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| Yong Chan Lee |
Professor of Medicine Director, Gastrointestinal Research Laboratory Veterans Affairs Medical Center, Univ. California San Francisco San Francisco, USA |
| Jong Pil Im | Seoul National University College of Medicine, Seoul, Korea |
| Robert S. Bresalier | University of Texas M. D. Anderson Cancer Center, Houston, USA |
| Steven H. Itzkowitz | Mount Sinai Medical Center, NY, USA |
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Albert J. Czaja
Correspondence to: Albert J. Czaja, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, 200 First Street S.W., Rochester, MN 55905, USA, Tel: +1-507-284-2691, Fax: +1-507-284-0538, E-mail: czaja.albert@mayo.edu
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Gut Liver 2016;10(2):177-203. https://doi.org/10.5009/gnl15352
Published online March 15, 2016, Published date March 15, 2016
Copyright © Gut and Liver.
Autoimmune hepatitis is characterized by autoantibodies, hypergammaglobulinemia, and interface hepatitis on histological examination. The features lack diagnostic specificity, and other diseases that may resemble autoimmune hepatitis must be excluded. The clinical presentation may be acute, acute severe (fulminant), or asymptomatic; conventional autoantibodies may be absent; centrilobular necrosis and bile duct changes may be present; and the disease may occur after liver transplantation or with features that suggest overlapping disorders. The diagnostic criteria have been codified, and diagnostic scoring systems can support clinical judgment. Nonstandard autoantibodies, including antibodies to actin, α-actinin, soluble liver antigen, perinuclear antineutrophil antigen, asialoglycoprotein receptor, and liver cytosol type 1, are tools that can support the diagnosis, especially in patients with atypical features. Prednisone or prednisolone in combination with azathioprine is the preferred treatment, and strategies using these medications in various doses can ameliorate treatment failure, incomplete response, drug intolerance, and relapse after drug withdrawal. Budesonide, mycophenolate mofetil, and calcineurin inhibitors can be considered in selected patients as frontline or salvage therapies. Molecular (recombinant proteins and monoclonal antibodies), cellular (adoptive transfer and antigenic manipulation), and pharmacological (antioxidants, antifibrotics, and antiapoptotic agents) interventions constitute future directions in management. The evolving knowledge of the pathogenic pathways and the advances in technology promise new management algorithms.
Keywords: Diagnosis, Atypical phenotypes, Autoantibodies, Treatment
Autoimmune hepatitis has diverse clinical phenotypes, and this diversity has complicated its diagnosis and management.1–5 The classical perception of autoimmune hepatitis as a chronic inflammatory liver disease that affects mainly young white women has been expanded,6–8 and diagnostic boundaries now encompass patients of both genders9,10 all ages,11–14 and various ethnic groups.5,15 Patients may have acute, acute severe (fulminant), or asymptomatic presentations; they may lack conventional serological markers; and they may have atypical histological features.1–5 Autoimmune hepatitis must now be considered in all patients with acute and chronic hepatitis of undetermined cause, including patients with graft dysfunction after liver transplantation.16–18
Diagnostic criteria have been codified, and diagnostic scoring systems have been developed to supplement clinical judgment in difficult cases.19–21 The repertoire of serological markers has been expanded to improve diagnosis, and investigational assays are evolving that may have prognostic implications.22–31 Corticosteroids alone or in combination with azathioprine are the mainstays of treatment,17,18,32–34 but regimens, involving calcineurin inhibitors, mycophenolate mofetil, and budesonide, have emerged from diverse clinical experiences as alternative front-line and salvage therapies.35–51 Furthermore, the clarification of pathogenic molecular and cellular interactions have suggested new, testable, therapeutic interventions.34,52–60
The goals of this review are to describe the nonclassical clinical phenotypes of autoimmune hepatitis, present the diagnostic criteria that have been formalized for this disease, indicate the current and evolving serological repertoire, present guidelines for the administration of conventional treatment regimens, outline strategies for incorporating nonstandard drugs in the treatment of selected patients, and indicate the site-specific molecular, cellular and pharmacological interventions that constitute future directions in the management of this disease.
An acute presentation occurs in 25% to 75% of patients with autoimmune hepatitis,61–65 and an acute severe (fulminant) presentation, characterized by the development of hepatic encephalopathy within 26 weeks of disease discovery, occurs in 3% to 6% of North American and European patients (Table 1).66,67 Each presentation can suggest an acute viral, toxic, or drug-induced liver injury, and each can delay recognition and proper treatment of autoimmune hepatitis.
Classical features of autoimmune hepatitis may be absent or less evident in patients with an acute severe (fulminant) presentation. Antinuclear antibodies (ANA) are undetected or weakly positive in 29% to 39% of patients,68,69 and serum immunoglobulin G (IgG) levels are normal in 25% to 39% of individuals (Table 1).25,69 Centrilobular hemorrhagic necrosis and massive or submassive liver necrosis dominate the histological findings in 86% of patients.67,68
Central perivenulitis with a prominent lymphoplasmacytic infiltrate and interface hepatitis supports the diagnosis of autoimmune hepatitis in 50% to 90% of patients with acute liver failure,67 and a histological assessment has been encouraged if liver tissue can be obtained safely.69,70 Heterogeneous hypoattenuated regions within the liver can be demonstrated by unenhanced computed tomography in 65% of patients with autoimmune hepatitis and acute liver failure, and these findings are disease-specific.61,71
Autoimmune hepatitis is asymptomatic in 25% to 34% of patients, and the diagnosis must be considered in all individuals with newly discovered mild liver test abnormalities (Table 1).72,73 Symptoms develop in 26% to 70% of patients within 2 to 120 months (mean interval, 32 months), and histological findings, including the frequencies of moderate to severe interface hepatitis (87% vs 93%), periportal fibrosis (41% vs 41%), and bridging fibrosis (39% vs 48%), are similar between asymptomatic and symptomatic individuals.73
Untreated patients with mild, asymptomatic, autoimmune hepatitis improve spontaneously less frequently (12% vs 63%, p=0.006) and less completely than treated patients with severe symptomatic disease during 77±31 months of observation,74 and they have a lower 10-year survival (67% vs 98%, p=0.01).74 The uncertainty that mild autoimmune hepatitis remains mild compels the consideration of corticosteroid therapy in all patients with the diagnosis.
Patients with typical clinical and laboratory findings of autoimmune hepatitis may lack ANA, smooth muscle antibodies (SMA), and antibodies to liver kidney microsome type 1 (anti-LKM1) (Table 1).75–77 The revised original scoring system of the International Autoimmune Hepatitis Group (IAIHG) has reclassified 34% of patients with cryptogenic chronic hepatitis as definite or probable autoimmune hepatitis in one European study,78 and two North American studies have indicated that 19% to 22% of patients with cryptogenic hepatitis can be categorized as autoimmune hepatitis by the scoring system of the IAIHG79 or by clinical judgment.80 Lower frequencies of autoantibody-negative autoimmune hepatitis (1% to 5%) have been reported in other studies applying different diagnostic criteria.81,82 Auto-antibody-negative autoimmune hepatitis has been a cause of acute liver failure in 7% of British patients83 and 24% of Japanese patients with acute severe (fulminant) presentations.84
Antinuclear antibodies and SMA may emerge later in the course of the disease;85,86 or nonstandard autoantibodies may be detected and support the diagnosis.75 Antibodies to soluble liver antigen (anti-SLA) occur in 9% to 31% of these patients;26,83,87 atypical perinuclear antineutrophil cytoplasmic antibodies (pANCA) support the diagnosis in some patients;88 and immunoglobulin A (IgA) antibodies to tissue transglutaminase or endomysium may implicate celiac disease as the basis for the liver dysfunction in other patients.89–93 The absence of autoantibodies does not preclude the diagnosis of autoimmune hepatitis or a benefit from corticosteroid therapy.75,76,81
Interface hepatitis is the
Bile duct injury may also be present with interface hepatitis.98–100 Biliary lesions that are isolated, unassociated with a cholestatic clinical syndrome, and unaccompanied by antimitochondrial antibodies (AMA) may constitute AMA-negative primary biliary cholangitis (PBC) or small duct primary sclerosing cholangitis (PSC).100–104 Bile duct injury, including destructive cholangitis (florid duct lesions), in conjunction with AMA in patients with otherwise classical features of autoimmune hepatitis may constitute an overlap syndrome between autoimmune hepatitis and PBC.102,105–107 Bile duct injury manifested by ductopenia, portal fibrosis, and portal edema suggests an overlap syndrome with PSC.102
Autoimmune hepatitis can recur or develop
Diagnostic criteria for recurrent or
Patients with autoimmune hepatitis and features classically associated with PBC (AMA and histological features of bile duct injury or loss) and PSC (absence of AMA and cholangiographic changes of focal biliary strictures and dilations) have an overlap syndrome (Table 1).106,129,130 Patients with autoimmune hepatitis may also have a cholestatic syndrome in the absence of classical features of PBC and PSC.99 These patients may have an overlap syndrome with AMA-negative PBC or small duct PSC.102,103,107
The overlap syndromes occur in approximately 10% of patients with otherwise classical features of autoimmune hepatitis.107 The major clinical consequence of the overlap syndromes is a variable response to conventional treatment regimens, and for this reason the diagnosis should be considered in all patients with refractory autoimmune hepatitis.106 Treatment is empiric and based on weak clinical evidence. Corticosteroids in combination with low dose ursodeoxycholic acid (13 to 15 mg/kg daily) is a common management strategy endorsed by the major liver societies.105,130–132
The gold standard for the diagnosis is clinical judgment, and the strongest independent predictor of an overlap syndrome is the liver tissue examination.133,134 The “Paris criteria” provide an objective basis for diagnosing the overlap syndrome between autoimmune hepatitis and PBC,105 and they have a sensitivity of 92% and specificity of 97% compared to clinical judgment.135
Formalized diagnostic criteria ensure the application of a standardized diagnostic algorithm,19 and diagnostic scoring systems provide an evaluation template that can support the diagnosis in difficult cases.19–21 All diagnostic guidelines recommend the performance of a liver tissue examination to establish the diagnosis.17,19,33,136 Retrospective studies that propose elimination of the diagnostic tissue examination have failed to evaluate its importance in excluding patients with similar features but other diagnoses.137,138
The diagnostic criteria of the IAIHG require the presence of compatible laboratory (serum aspartate [AST] and alanine aminotransferase [ALT] abnormalities, hypergammaglobulinemia, and increased serum IgG level), serological (ANA, SMA or anti-LKM1 positivity) and histological findings (interface hepatitis with or without plasma cell infiltration).19 Diseases that can resemble autoimmune hepatitis must also be excluded by appropriate tests, and these include virus-related, drug-induced, alcoholic, hereditary (Wilson disease, hereditary hemochromatosis), metabolic (nonalcoholic fatty liver disease [NAFLD]), and immune-mediated cholestatic diseases (PBC and PSC).19 The designation of definite or probable autoimmune hepatitis reflects the level of confidence in the diagnosis based on the compatibility of the clinical features with classical autoimmune hepatitis. Two scoring systems are available for challenging cases.19,20
The revised original scoring system is a comprehensive template that evaluates 13 clinical categories and renders 27 possible grades (Table 2).19 This comprehensive scoring system was originally developed as a research tool by which to ensure the homogeneity of patient populations in clinical studies.139 It has emerged subsequently as a template by which to ensure the systematic evaluation of patients, and it can serve as a mechanism by which to bolster clinical judgment.21,140 The scoring system can accommodate deficiencies or inconsistencies in the clinical presentation and support the diagnosis in difficult cases by rendering a composite score before and after corticosteroid treatment.
A simplified scoring system has been developed to ease clinical application.20 It evaluates four clinical categories and renders nine possible grades (Table 3).20 The original revised scoring system has greater sensitivity for autoimmune hepatitis (100% vs 95%),21 whereas the simplified scoring system has superior specificity (90% vs 73%) and accuracy (92% vs 82%), using clinical judgment as the gold standard.21 The simplified scoring system does not grade the treatment response, and this difference may contribute to its lower sensitivity.141 The revised original scoring system reclassifies patients with cryptogenic hepatitis as autoimmune hepatitis more commonly than the simplified scoring system (95% vs 24%), whereas the simplified scoring system excludes the diagnosis of autoimmune hepatitis more frequently in liver diseases that have concurrent immune manifestations (83% vs 64%).21
The diagnostic scoring systems have been extensively evaluated and refined by retrospective analyses of patients that have been characterized in single medical centers and diagnosed by experts in autoimmune liver disease.20,21,140–143 These characterizations have not followed a predefined protocol; pooled experiences have been limited; and comparative studies between medical centers have not been performed.141 Furthermore, assessments have not always been uniform or complete in each patient.20 Collaborative prospective clinical studies that adhere to a pre-established protocol and that ensure a uniform and complete assessment of each patient are necessary to validate the scoring systems.
The scoring systems have been applied beyond their original design and intention. They have been used inappropriately to determine the presence of autoimmune hepatitis in patients with PBC,144–146 and this application has been discouraged.130 The scoring systems have also been used but not validated in patients with acute severe (fulminant) liver failure141,147 and in patients with graft dysfunction after liver transplantation.113
The performance parameters of the revised original and simplified scoring systems for autoimmune hepatitis are based on their compatibility with the gold standard of clinical judgment.19–21,140 The results of these scoring systems can never supersede clinical judgment, and they cannot make a clinically untenable diagnosis tenable. Misapplication of the scoring systems and overinterpretation of their results are major pitfalls that must be avoided.
Antinuclear antibodies, SMA, and anti-LKM1 characterize most patients with autoimmune hepatitis, and they should be assessed in all candidates for the diagnosis (Table 4).17 Antinuclear antibodies and SMA are usually present in the absence of anti-LKM1, and anti-LKM1 are usually detected in the absence of ANA and SMA.148,149 This exclusivity has justified the designations of type 1 autoimmune hepatitis for those patients with ANA and/or SMA, and type 2 autoimmune hepatitis for those patients with anti-LKM1.148
The subtypes of autoimmune hepatitis have been associated with different age groups148 and genetic predispositions,150–153 but they have not been associated with major differences in treatment outcomes.17,33,154 Accordingly, the subtypes have not been endorsed as valid pathological entities. Indeed, among adults with autoimmune hepatitis, there have been no significant clinical, laboratory, histological, genetic or outcome differences to justify a designation of type 1 and type 2 autoimmune hepatitis.155
Antinuclear antibodies and SMA lack disease- and organ-specificity (Table 4). Antinuclear antibodies are present in 80% of patients with autoimmune hepatitis, and SMA occur in 63%.156 These antibodies also occur commonly in other liver diseases. Antinuclear antibodies are present in 20% to 40% of patients with alcoholic liver disease, NAFLD, chronic viral hepatitis, PBC or PSC.156–158 Smooth muscle antibodies occur in 3% to 16% of patients with alcoholic liver disease, NAFLD, chronic hepatitis C, PBC or PSC.156–158 Each autoantibody has low sensitivity for the diagnosis (32% for ANA and 16% for SMA) when present as an isolated finding.156 The performance parameters of ANA and SMA are enhanced if both autoantibodies are present. The concurrence of ANA and SMA has a sensitivity of 43%, specificity of 99%, and diagnostic accuracy of 74% for autoimmune hepatitis.156
Antinuclear antibodies seem to be the most variable marker during the course of the disease,86 whereas SMA in titers >1:80 are associated with laboratory (77%) and histological (100%) activity.159 Antinuclear antibodies are reactive against multiple nuclear components, including centromere, ribonucleoproteins, ribonucleoprotein complexes and histones, and 46% of patients with ANA have multiple nuclear reactivities.160,161 Smooth muscle antibodies in autoimmune hepatitis are directed mainly against filamentous (F) actin, but nonactin reactivities are present in 14% of patients with SMA.162
Antibodies to LKM1 are present in 3% of North American adults149,156 and 14% to 38% of British children with autoimmune hepatitis (Table 4).11,163 They can also be demonstrated in 0% to 2% of North American patients156,164 and 10% of European patients with chronic hepatitis C.165,166 Antibodies to LKM1 have a sensitivity of only 1% for autoimmune hepatitis in North American adults, but their specificity is 99% and their diagnostic accuracy is 57%. Only 2% of patients with ANA or SMA have anti-LKM1.156 The cytochrome mono-oxygenase, P450 2D6, is the target antigen of anti-LKM1.167,168
The nonstandard autoantibodies constitute a repertoire of serological markers that can support or extend the diagnosis of autoimmune hepatitis to highly selected individuals in whom the standard biomarkers are insufficient to render a diagnosis.169–171 The presence of nonstandard autoantibodies can upgrade the diagnosis of autoimmune hepatitis by the revised original diagnostic scoring system of the IAIHG.17,19
Antibodies to actin (antiactin) are directed against filamentous (F) actin, and they are present in 87% of patients with autoimmune hepatitis (Table 5).162,170,172 They also occur in diverse immune-mediated, nonliver diseases, including systemic lupus erythematosus, Sjögren syndrome, rheumatoid arthritis, celiac disease, diabetes, autoimmune thyroiditis and Crohn’s disease.170 Antibodies to actin are a subset of SMA, and 86% to 100% of patients with autoimmune hepatitis and SMA have antiactin.162,173 Both SMA and antiactin are indirect markers of laboratory and histological activity in autoimmune hepatitis.159
Most patients with antiactin have at least SMA or other conventional autoantibodies, and the detection of antiactin is not critical for the diagnosis.162 Antibodies to actin have been associated with a higher frequency of death from hepatic failure or requirement for liver transplantation, but the prognostic implications of these antibodies are assay dependent.27,30,162,173–176 Multiple assays for antiactin are available, but none has been incorporated into a standard diagnostic repertoire.162,177
α-Actinins are cross-linking proteins that bind to actin and that are expressed as isoforms in muscle and nonmuscle cells.178 Antibodies to α-actinin have been found by enzyme-linked immunosorbent assay (ELISA) in 42% of patients with autoimmune hepatitis compared to 13% of patients with other liver diseases and 6% of healthy blood donors (Table 5).27 Antibodies to α-actinin are present in 66% of patients with autoimmune hepatitis who are positive for antifilamentous actin (anti-F actin), and the combination seems to be specific for the disease.27
Double reactivity to anti-F-actin and anti-α-actinin seems to have prognostic implications. Patients with both antibodies have clinical and histological activity and a severe form of the disease characterized by an acute onset.27 Patients who respond to corticosteroid regimens have lower baseline levels of anti-α-actinin than patients who relapse or respond incompletely, and the baseline level of anti-α-actinin has been an independent predictor of treatment response.30 The assay for anti-α-actinin is still investigational and not generally available.27,30
Antibodies to soluble liver antigen (anti-SLA) are present in 7% to 22% of patients with autoimmune hepatitis, and their occurrence varies among different ethnic groups (Table 5).26,31,87,179,180 Antibodies to soluble liver antigen seem to be least common in Japanese patients (7%)26 and most common in German patients (19% to 22%).26,87 The variability in serological expression may have a genetic basis, and anti-SLA have been associated with human leukocyte antigen (HLA) A1-B8 in Germany87 and HLA DRB*0301 in Britain25 and the United States.24
Antibodies to soluble liver antigen have high specificity for autoimmune hepatitis (99%),179 and they have been the sole marker of autoimmune hepatitis in 14% to 20% of patients who would otherwise have been classified as cryptogenic hepatitis.159,180,181 They also have been associated with more severe histological findings, longer treatment requirement to suppress inflammatory activity, increased frequency of relapse after drug withdrawal, and higher frequency of liver transplantation or death from liver failure than patients without this marker.24–26,87,179 The target antigen of anti-SLA is a transfer ribonucleic acid (RNA)-protein complex, now designated as SEPSECS (Sep [O-phosphoserine] tRNA:Sec [selenocysteine] tRNA synthase).23,182,183 Antibodies to soluble liver antigen have also been closely associated with antibodies to ribonucleoprotein/Sjögren syndrome A antigen (anti-Ro/SSA), and the clinical implications of this tightly linked expression (96% concurrence) remains unclear.31,184–186
Atypical pANCA are detected in 50% to 92% of patients with autoimmune hepatitis, often in high titer (mean titer, 11,410±1,875),88,187–189 and serum titers are not associated with laboratory tests of disease activity (serum AST, IgG, and γ-globulin levels).88 Atypical pANCA exhibit some selectivity in that they are absent in anti-LKM1-positive autoimmune hepatitis,190 but they can occur in chronic ulcerative colitis, PSC, PBC, chronic hepatitis C, and minocycline-induced autoimmune disease.187,188,191–193
The primary target antigen has been characterized as a 50 kDa protein on the inner side of the nuclear envelope,191 and it has been identified as β-tubulin isotype 5.189 Ninety-seven percent of patients with pANCA and autoimmune hepatitis have atypical pANCA, and 88% of the pANCA-positive patients have reactivity to β-tubulin isotype 5.189 The pANCA of autoimmune hepatitis also cross-react with an evolutionary precursor bacterial protein, FtsZ, and 82% of pANCA-positive patients with autoimmune hepatitis have reactivity to both proteins.189 These dual reactivities have justified speculation that intestinal micro-organisms trigger an immune response that results in liver inflammation in genetically susceptible individuals.189,194
The assessment of atypical pANCA has been included in the comprehensive diagnostic scoring system for autoimmune hepatitis,19 and the autoantibodies may be useful in developing the diagnosis of autoimmune hepatitis in patients who are otherwise seronegative and classified as cryptogenic chronic hepatitis.17,76,171,195 The presence of atypical pANCA has been associated with cirrhosis187 and relapse after corticosteroid withdrawal in autoimmune hepatitis,196 but the prognostic implications of atypical pANCA in autoimmune hepatitis have not been sufficiently established to warrant their routine assessment.17,88,197
Antibodies to the asialoglycoprotein receptor (anti-ASGPR) are present in 67% to 88% of patients with autoimmune hepatitis (Table 5).28,198–201 They occur in adults and children with autoimmune hepatitis, and they do not have an exclusive serological profile.202 Antibodies to the asialoglycoprotein receptor can be present in acute hepatitis A (57%), acute hepatitis B (35%), PBC (14% to 100%), chronic hepatitis C (14%), alcoholic liver disease (8%), and chronic hepatitis B (7%).28,198,199,203,204 The lack of disease specificity has compromised the diagnostic function of anti-ASGPR, and the major value of this serological marker may be in the assessment of patients who are seronegative for the conventional markers of autoimmune hepatitis.205
Antibodies to asialoglycoprotein receptor can disappear during corticosteroid therapy, and the disappearance has been associated with histological resolution.206 Patients with anti-ASGPR during corticosteroid therapy also have a higher frequency of relapse after drug withdrawal than patients in whom anti-ASGPR has disappeared or never been expressed (88% vs 33%, p=0.01).201,206 These attributes suggest that anti-ASGPR may be useful in defining end points of treatment.28 The inability to standardize the assay for anti-ASGPR has been the major limitation to its broad clinical application.28,199,201,207
Antibodies to liver cytosol type 1 (anti-LC1) co-exist with anti-LKM1 in 24% to 32% of patients with anti-LKM1-positive au-toimmune hepatitis (Table 5).208–210 They are also present in 12% to 33% of patients with chronic hepatitis C and anti-LKM1,211–214 and they occur infrequently in patients with autoimmune hepatitis and SMA and/or ANA.215 Antibodies to liver cytosol type 1 occur mainly in European children and young adults aged ≤20 years,209,210 and they are rarely found in white North American adults.216 Antibodies to liver cytosol type 1 may be the sole markers of autoimmune hepatitis in patients seronegative for SMA, ANA, and anti-LKM1,217,218 but this diagnostic role may be limited, especially in North American adults in whom the frequency of anti-LC1 has been low.216 Formiminotransferase cyclodeaminase is a cytosolic enzyme that has been identified as the target antigen of anti-LC1.219–222
Prednisone or prednisolone alone or in combination with azathioprine is the mainstay therapy of autoimmune hepatitis (Table 6).17,33 Combination therapy is preferred as lower doses of corticosteroid can be administered when combined with azathioprine, and the frequency of corticosteroid-related side effects is lower (10% vs 44%).223 Both regimens have otherwise similar outcomes.223 All patients with active autoimmune hepatitis are candidates for treatment regardless of symptom status (symptomatic versus asymptomatic) or disease severity (mild versus severe).34,74
Combination therapy is appropriate for most patients, especially those with an anticipated low tolerance for corticosteroids (individuals with obesity, diabetes, hypertension, osteopenia, or emotional instability).34 Monotherapy with corticosteroids is appropriate for patients with a known or anticipated intolerance of azathioprine (individuals with severe cytopenia [leukocyte count, <2.5×109/L; platelet count, <50×109/L], thiopurine methyltransferase deficiency [TPMT], or pregnancy) and for patients with acute severe autoimmune hepatitis or manifestations of acute liver failure.34
The immunosuppressive actions of azathioprine develop slowly over a 6-week period,224,225 and monotherapy with prednisone or prednisolone may have a more rapid action than combination therapy in patients with acute severe disease.49 Azathioprine is a category D drug for pregnancy in the United States, and congenital malformations have occurred in animal studies.226 Furthermore, azathioprine metabolites can pass the human placenta,227 and the drug has been of concern in the occurrence of human fetal complications.228 These concerns have been strongly counterbalanced by numerous studies in azathioprine-treated women with inflammatory bowel disease in whom the rarity or nonexistence of azathioprine-related fetal complications has been documented.184,229–233 Importantly, azathioprine is not an essential drug in the management of autoimmune hepatitis during pregnancy, and the drug can be replaced in pregnancy by an adjusted dose of prednisone or prednisolone.17,138
The preferred treatment regimen combining corticosteroids and azathioprine consists of an induction phase and a maintenance phase (Table 6).34 During the 4-week induction phase, prednisone or prednisolone, 30 mg daily, is administered for 1 week. The dose is then reduced to 20 mg daily for 1 week and 15 mg daily for 2 weeks. Azathioprine, 50 mg daily, is given as a fixed dose during the entire induction phase. After 4 weeks of induction, the dose of prednisone or prednisolone is adjusted to 10 mg daily. The dose of azathioprine is maintained at 50 mg daily. The maintenance phase is continued at fixed doses of prednisone or prednisolone, 10 mg daily, and azathioprine, 50 mg daily, until normalization of serum AST, ALT, bilirubin, and γ-globulin or IgG levels and resolution of the histological abnormalities.17 In Europe, prednisolone is preferred over prednisone, and it is commonly administered in a weight-based dose (up to 1 mg/kg daily) during the induction phase. Similarly, the dose of azathioprine is commonly weight-based (1 to 2 mg/kg daily).33,234,235
Blood leukocyte and platelet counts must be monitored throughout the induction and maintenance phases at 3 to 6 month intervals.17 Progressive cytopenia warrants the reduction or discontinuation of azathioprine. The determination of TPMT activity prior to treatment can identify the 0.3% of the normal population with absent TPMT activity.236 These patients are at risk for azathioprine-induced myelosuppression.138,237 Routine genotyping or phenotyping for TPMT activity has not correlated closely with the occurrence of azathioprine toxicity except in those patients with absent enzyme.238–240 Close monitoring of the clinical and hematological findings has been emphasized for all patients receiving this medication.17
Monotherapy with prednisone or prednisolone involves a 4-week induction phase and then a fixed-dose maintenance phase (Table 6).17 During the 4-week induction phase, prednisone or prednisolone, 60 mg daily, is administered for 1 week. The dose is then reduced to 40 mg daily for 1 week and 30 mg daily for 2 weeks.34 After 4 weeks of induction, the dose of prednisone or prednisolone is reduced to 20 mg daily, and the regimen is maintained until resolution of clinical, laboratory and histological findings.34 An adjuvant program of regular weight-bearing exercise, vitamin D and calcium supplementation, and treatment with bisphosphonates (if justified by bone densitometry or clinical history of bone disease) may protect against progressive corticosteroid-related osteopenia.17
Treatment is continued until normal laboratory tests and liver tissue.17 Normal liver tests are achieved in 66% to 91% of patients within 2 years.138,235,241 The average treatment duration until normal liver tests and normal or near-normal liver tissue is 22 months. Treatment may be extended for ≥3 years, but the frequency of remission decreases to 14% and progression to cirrhosis (54% vs 18%, p=0.03) and need for liver transplantation (15% vs 2%, p=0.048) increases compared to patients who respond fully within 12 months.242
In Europe, treatment is usually continued for at least 2 years before any decision regarding the discontinuation of therapy.235 Histological improvement commonly lags behind clinical and laboratory improvement by 3 to 8 months, and treatment should be continued beyond laboratory resolution before any attempt at drug withdrawal.243 Liver tissue examination is the preferred method of documenting histological resolution, but stable normal laboratory tests for 12 to 18 months may be sufficient to indicate the absence of histological activity and justify the termination of treatment.33
The decision to discontinue therapy must balance the possibility of a sustained long-term drug-free remission against the risk of relapse and the need for retreatment.244 The frequency of achieving a treatment-free state is 19% to 40% in studies of at least 3 years duration80,245–248 and 36% in studies of at least 5 years duration.248 The frequency of relapse after drug withdrawal is 50% to 87% depending on duration of follow-up.246,249,250 Relapse has been associated with progressive hepatic fibrosis in 10% and clinical deterioration in 3%, but in most instances relapse can be effectively treated with the prompt resumption of treatment.251
Ultimately, the decision to stop treatment must be based on patient preferences and the physician’s ability to monitor for relapse and promptly restart treatment if necessary.244 Drug withdrawal can be attempted under close monitoring, and the original treatment regimen can be rapidly resumed if serum aminotransferase levels increase. A rapid and complete response to retreatment can be anticipated (Table 6).249 A long term maintenance regimen can then be instituted after normalization of liver tests by increasing the dose of azathioprine to 2 mg/kg daily and gradually withdrawing the corticosteroid.17,32
Liver tests worsen during therapy (treatment failure) in 7% of patients,252 and they improve but not to normal levels (incomplete response) in 14%.242,253 Treatment-ending side effects associated with corticosteroid therapy occur in 12% to 29%, and they are mainly intolerable cosmetic changes, obesity, emotional instability, and vertebral compression.74,245,254 Treatment ending side effects associated with azathioprine therapy occur in 5% to 10% of patients, and they are mainly nausea, vomiting, rash, cytopenia (≤6%), pancreatitis, and liver toxicity.223,254,255 Patients with cirrhosis develop corticosteroid-induced side effects more commonly than patients without cirrhosis (25% vs 8%) presumably because of increased systemic levels of unbound (free) prednisolone,48,223 and they develop cytopenia that can suggest azathioprine toxicity more often (70% vs 26%, p<0.0001).239,240
Patients who fail conventional treatment are treated with high doses of the original medication (Table 6). The dose of prednisone or prednisolone is increased to 30 mg daily and the dose of azathioprine is increased to 150 mg daily.18,34,39,253,256 Patients receiving monotherapy are treated with prednisone or prednisolone, 60 mg daily. Treatment is continued at a fixed dose for one month. Thereafter, the doses of medication are reduced by 10 mg of prednisone or prednisolone and 50 mg of azathioprine after each month of laboratory and clinical improvement until conventional maintenance levels for that particular regimen are reached.
The inability to improve tests after 1 month justifies continuation of the medication in unaltered dose. Worsening of clinical or laboratory status after a dose reduction warrants an increase in the dose to the last level associated with improvement, and the regimen should be maintained for another month until an improvement warrants another attempt at dose reduction. Clinical and laboratory features improve in 70% to 100% of patients; laboratory resolution occurs in 35%; and treatment withdrawal is possible in 20% to 35%.39,257 Most patients remain on therapy indefinitely, and they are at risk for progression of their liver disease and the development of treatment-related side effects. Refractory progressive disease and manifestations of liver failure compel an evaluation for liver transplantation.
Patients who have not achieved clinical, laboratory and histological normality after 36 months of conventional treatment can be classified as having an incomplete response.242 They are unlikely to achieve complete resolution with additional treatment, and the risk of drug-induced side effects increases. Management can be adjusted to prevent progression of the disease with the lowest tolerated dose of medication possible (Table 6). Therapy with prednisone or prednisolone, 10 mg daily, in combination with azathioprine, 2 mg/kg daily, can be started, and the doses can be gradually decreased to maintain a normal or near-normal serum AST level.253 Treatment is indefinite, and the final regimen may consist of low dose corticosteroid in combination with azathioprine or monotherapy with dose-adjusted azathioprine or corticosteroid.32,258,259
Patients with drug-intolerance are treated by decreasing the dose of the toxic medication or discontinuing its use (Table 6).17,253 The dose of the tolerated medication can be adjusted to suppress inflammatory activity. Mycophenolate mofetil (1 to 2 g daily) has been used for azathioprine intolerance, and it has successfully replaced azathioprine in 58% of cases.41,45,46,49,50 Mycophenolate mofetil has side effects in 3% to 34% of patients, including cytopenia, which may resemble those of azathioprine, and it should be administered with caution or avoided in cytopenic patients.49,260,261 It also has well documented teratogenic effects that preclude its use in pregnancy.262–265
Budesonide, mycophenolate mofetil, and the calcineurin inhibitors (cyclosporine and tacrolimus) have been used as alternative frontline and salvage therapies in autoimmune hepatitis.34 Budesonide has emerged mainly as an alternative frontline therapy in selected patients, whereas mycophenolate mofetil and the calcineurin inhibitors have been used mainly as salvage therapies.34
Budesonide (6 to 9 mg daily) in combination with azathioprine (1 to 2 mg/kg daily) has been shown by randomized clinical trial to normalize serum AST and ALT levels more frequently (47% vs 18%) and with fewer side effects (28% vs 53%) than conventional combination therapy with prednisone (40 mg daily tapered to 10 mg daily) and azathioprine (1 to 2 mg/kg daily) when administered for 6 months (Table 7).44 The histological response has not been documented; the durability of the response is unclear; and the low frequency of laboratory response (18%) and high frequency of side effects (53%) in the patients receiving conventional corticosteroid therapy are unexplained. Nevertheless, budesonide, a next generation glucocorticoid, in combination with azathioprine has emerged as an alternative frontline treatment for autoimmune hepatitis.34
Subset analyses of children randomized to each regimen have disclosed similar frequencies of laboratory resolution (16% vs 15%) and side effects (47% vs 63%) between the budesonide and standard regimens.266 For this reason, the superiority of budesonide therapy over standard treatment to induce remission in juvenile patients has been questioned.267 These observations indicate that budesonide therapy can have variable effects in different populations and that careful patient selection may be the key determinant of outcome.
Therapy with budesonide has been associated with the development of corticosteroid-induced complications in patients with cirrhosis,268,269 break-through exacerbations of the liver disease during treatment that have required standard therapy,270 and severe arthralgias and myalgias in patients previously treated with prednisone that have justified readministration of the standard drug regimen.271 Combination therapy with budesonide and azathioprine may be most appropriate in treatment-naïve patients with mild liver inflammation, early stage disease, and absence of concurrent immune diseases. The presence of obesity, diabetes, hypertension, or osteopenia that might be worsened by prednisone treatment also support consideration of the budesonide regimen.34
Mycophenolate mofetil, a next generation purine antagonist, has been used as a frontline and salvage therapy for autoimmune hepatitis.34 As a frontline treatment in 59 patients treated for 3 to 92 months (mean, 26 months), mycophenolate mofetil (1 g daily adjusted to a final dose of 1.5 to 2 g daily) in combination with prednisolone (0.5 to 1 mg/kg daily followed by a tapered withdrawal) normalized serum ALT and γ-globulin levels in 88%, induced a partial laboratory improvement in 12%, allowed the withdrawal of corticosteroids in 58%, and induced treatment-ending side effects in 3% (Table 7).47 Therapy with mycophenolate mofetil and prednisolone can be effective and safe in treatment-naïve patients, but comparative clinical trials with standard therapy are necessary to establish its preference.
Mycophenolate mofetil has also been used as a salvage therapy for patients with corticosteroid-refractory liver disease or azathioprine intolerance.34 Composite analysis of the several, small, single center experiences indicates that mycophenolate mofetil can induce improvement of laboratory tests in 45%, facilitate the withdrawal of corticosteroids in 40%, and cause treatment-ending side effects in 15% (Table 7).34,50 Outcomes can be improved by using the treatment in a selective fashion. Therapy with mycophenolate mofetil has rescued patients who are azathioprine intolerant more commonly than patients who are refractory to conventional corticosteroid treatment (58% vs 23%),34,41,45,46,50 whereas children with autoimmune hepatitis and sclerosing cholangitis have not responded.
Caveats that must be considered before instituting therapy include recognition than the drug is 6 to 7 times more expensive than azathioprine, treatment is commonly indefinite, side effects develop in 3% to 34%, and pregnancy is an absolute contraindication to its use.49,272,273
Cyclosporine has been used successfully as a frontline agent in children and adults with autoimmune hepatitis,36,274,275 but the only randomized clinical trial involving 39 patients has indicated equivalency rather than superiority of cyclosporine therapy to standard combination therapy (Table 7).51 In the absence of clear advantages that outweigh the risks of treatment (hypertension, nephrotoxicity, infection, pancreatitis, neurotoxicity and malignancy) and its expense, frontline therapy with cyclosporine cannot be justified.49 Similarly, tacrolimus (3 mg twice daily) has also had success as a frontline treatment in 21 patients who improved their serum ALT and AST levels after 3 months.35 The cytopenia and nephrotoxicity that developed in these patients were not treatment-ending, but validation of this regimen by randomized clinical trial has not emerged after 20 years.
The calcineurin inhibitors have also been used successfully to salvage patients with corticosteroid-refractory autoimmune hepatitis.34 Composite clinical experiences with cyclosporine in 22 such patients have indicated improvement of variable degree in 93% and failure of response due to recalcitrance, drug toxicity, or noncompliance in 7%.49,50 Similarly, composite experiences with tacrolimus involving 44 patients have indicated improvement in 87% and failure of response in 13%.35,38,50,276 The calcineurin inhibitors have been associated with serious side effects, including a paradoxical heightened state of autoreactivity, and endorsement of these agents as rescue therapies has not been universal.49,277 Furthermore, the calcineurin inhibitors have mainly immunosuppressive rather than anti-inflammatory effects, and they have not been effective in preventing autoimmune hepatitis after liver transplantation.113,278
Treatment with the calcineurin inhibitors is commonly indefinite, and it requires experience to ensure careful monitoring and appropriate dose adjustment. Cyclosporine (Neoral) has been administered in doses of 2 to 5 mg/kg body weight with dose adjustments to achieve trough levels of 100 to 300 ng/mL,34,36,49 and tacrolimus has been administered at a starting dose of 0.5 to 1 mg daily and increased to 1 to 3 mg twice daily as tolerated to achieve a serum level of 3 ng/mL (range, 1.7 to 10.7 ng/mL).34,35,38,49,276,279
Small clinical experiences with rapamycin (sirolimus), rituximab, and infliximab have illustrated the continuing effort that is being expended to develop rescue therapies that can supplant or supplement current corticosteroid-based regimens for auto-immune hepatitis.34,49,54,253 Rapamycin (1 to 3 mg daily adjusted to maintain blood levels of 5 to 8 μg/dL) has suppressed the inflammatory manifestations of six patients with recurrent or
Rituximab has improved isolated cases of autoimmune hepatitis with idiopathic thrombocytopenic purpura,281 cryoglobulinemic glomerulonephritis,282 previous B cell lymphoma,283 and Evans syndrome (hemolytic anemia and idiopathic thrombocytopenia),284 and rituximab (two infusions of 1,000 mg 2 weeks apart) has reduced serum AST levels in all six treated patients, improved histological features in four biopsied patients, and allowed corticosteroid withdrawal in three of four patients in a small treatment trial (Table 8).285
Similarly, a small trial of infliximab (infusions of 5 mg/kg body weight at time zero, 2 weeks, 6 weeks, and every 4 to 8 weeks thereafter) in 11 patients with refractory autoimmune hepatitis has normalized liver tests in eight patients, improved histological activity indices in five patients, and allowed treatment withdrawal in three patients (Table 8).55 The development of side effects (mainly infectious complications) in seven of the 11 patients receiving infliximab, including three patients (27%) who required discontinuation of the drug, underscores the importance of establishing safety profiles, dosing guidelines, and monitoring strategies for each drug under trial before considering routine clinical application.286–291
Liver transplantation is the ultimate rescue therapy for patients that present with features of liver failure or who develop these features during standard treatment.256 The 5- and 10-year patient survivals after liver transplantation exceed 70% in adults,118,292–294 and the 5-year survival is as high as 86% in children.295 Recurrent disease can progress to cirrhosis,296 and 13% to 50% of adults with recurrent disease develop graft failure.115,297,298 Retransplantation may be necessary with the understanding that autoimmune hepatitis may still recur.115,296 Importantly, serious consequences of recurrent autoimmune hepatitis have not been uniformly experienced in all centers. The actuarial 5-year survivals for patients and grafts after recurrent autoimmune hepatitis have been 100% and 87% in one experience,115 and patient and graft survivals have been similar to those of patients transplanted for nonautoimmune liver diseases in other experiences.118,297,299 The risk of recurrent auto-immune hepatitis after liver transplantation should not affect the transplant decision. Liver transplantation is indicated by a model of end-stage liver disease (MELD) score >16 points, acute decompensation, intractable symptoms, treatment intolerance, or detection of liver cancer.293
Most new therapeutic interventions have not moved beyond the theoretical stage in autoimmune hepatitis, but their premise and promise are founded on studies already performed in cell cultures, animal models, or preliminary clinical trials in other immune-mediated diseases.34,52,53,300,301 They await rigorous study in autoimmune hepatitis.
Monoclonal antibodies to tumor necrosis factor-α (infliximab)55 and monoclonal antibodies to CD20 (rituximab)285 have already begun an evaluation process in the treatment of autoimmune hepatitis (Table 8). Other molecular interventions that have advanced in animal studies and clinical trials outside autoimmune hepatitis also warrant consideration in this disease. Molecular interventions are intended to blunt or correct detrimental pathological mechanisms, but they may also interfere with normal homeostatic mechanisms and have unintended consequences. Their introduction as therapeutic agents requires an awareness of these possible consequences and rigorous evaluation in clinical trials.
Cytotoxic T lymphocyte antigen-4 fused with immunoglobulin (CTLA-4Ig) is a dimeric recombinant human fusion protein that is a homologue of the CD28 molecule expressed on the surface of CD4+ T lymphocytes (Table 8).52 CTLA-4Ig can interfere with the binding of CD28 with the B7 ligands (CD80 and CD86) expressed on antigen-presenting cells and prevent completion of the signaling pathway necessary for lymphocyte activation.302 CTLA-4Ig is already approved for use in rheumatoid arthritis, and it has improved the serological and histological manifestations of PBC in a murine model.303
Nonmitogenic monoclonal antibodies to CD3 target the T cell antigen receptor of T lymphocytes, and they can promote the apoptosis of immune cells (Table 8).300,304 The newly released apoptotic bodies can then be ingested by macrophages and dendritic cells, and these cells can in turn produce transforming growth factor β (TGF-β).305 Regulatory T cells that express the latency-associated peptide can be induced by TGF-β and expand the immunosuppressive effect.306 Antibodies to CD3 have already been shown to induce complete and durable remission in nonobese diabetic mice,307 and clinical trials have demonstrated its effectiveness in maintaining or increasing insulin production in patients with insulin-dependent autoimmune diabetes.308
Simtuzumab (GS-6624) is a monoclonal antibody that is directed against the enzyme that promotes the cross-linkage of collagen fibrils and expansion of extracellular matrix (Table 8). Simtuzumab has been safe and well-tolerated in Phase 1 studies involving patients with hepatic fibrosis, and this monoclonal antibody to lysyl oxidase-like 2 has entered Phase 2 clinical studies designed to prevent hepatic fibrosis in NAFLD and PSC (
Regulatory T cells and natural killer T cells are cell populations that help modulate immune reactivity, and they have been manipulated to suppress inflammatory and immune responses in animal models of diverse immune-mediated diseases (Table 8).59,300 Regulatory T cells can be expanded by pharmacological agents (corticosteroids, rapamycin, mycophenolate mofetil, and 1, 25 dihydroxyvitamin D3)59 or by the adoptive transfer of autologous cells that have been expanded or newly generated
Natural killer T cells have stimulatory and inhibitory actions on the innate and adaptive immune responses, and they are amenable to manipulation by antigenic stimuli that promote the desired predominant action (Table 8).59,300,314 Natural killer T cells expressing a semi-invariant antigen receptor recognize glycolipid antigens bound to the CD1 antigen-presenting molecule, and glycolipid antigens can be designed to elicit the preferred action of these cells.315 Natural killer T cells have been evaluated in animal models of type 1 diabetes, systemic lupus erythematosus, rheumatoid arthritis, and autoimmune encephalomyelitis,300 and studies in experimental autoimmune hepatitis have supported the further investigation of their pathogenic role and therapeutic implications in this disease.316,317
Mesenchymal stromal cells also affect the innate and adaptive immune responses by modulating the activity of macrophages, natural killer cells, and dendritic cells and by inhibiting the activity of B and T lymphocytes (Table 8).60 The adoptive transfer of mesenchymal stromal cells has been effective in murine models of rheumatoid arthritis and radiation-induced liver injury,301,318 and its therapeutic promise has been supported by preliminary human experiences in refractory Crohn’s disease, corticosteroid-resistant graft-versus-host disease, and allograft rejection after kidney transplantation.319–321 Serious side effects have not been encountered in mid-term human studies, but questions remain regarding the preferred expansion technique, the rare occurrence of immunogenicity in animal models, and the possible induction of chromosome aberrations, transient aneuploidy, or malignant transformations in cell cultures from murine and human sources.60 There have been no reported experiences in autoimmune hepatitis.320
The generation of reactive oxygen species from Kupffer cells and myofibroblasts promotes the apoptosis of hepatocytes, the release of apoptotic bodies, and the activation of hepatic stellate cells.322,323 Antioxidants (N-acetylcysteine, S-adenosyl-L-methionine, and vitamin E) have already been shown in clinical experiences to decrease histological activity, TGF-β production, and fibrosis in NAFLD (Table 8).324,325 They have also improved mortality in alcoholic cirrhosis,326 and enhanced early viral responses in chronic hepatitis C.327 Angiotensin inhibitors may inhibit the transformation of hepatic stellate cells into myofibroblasts, and losartan has decreased fibrosis in chronic hepatitis C.328 The antioxidants and the angiotensin inhibitors are feasible antiapoptotic and antifibrotic agents that warrant evaluation as adjunctive therapies in autoimmune hepatitis.329–332
Agents that reduce apoptosis are feasible interventions in autoimmune hepatitis if their actions can be directed to the pertinent cell population. Caspase inhibitors have reduced apoptosis in murine models of acute liver injury,333 bile duct ligation,334 NAFLD,335 and acute liver failure after massive hepatectomy.336 They have also been used in limited clinical experiences involving patients with chronic hepatitis C337,338 and NAFLD337 and in organs for liver transplantation to protect against ischemia/re-perfusion injury.339 The major concern is the possibility of unintended interference with normal apoptotic pathways that guard against the invasion of pathogens and the malignant transformation of cells.57 Caspase inhibitors have not been evaluated in autoimmune hepatitis.
Patients with chronic liver disease, including autoimmune hepatitis, have reduced serum levels of 25-hydroxyvitamin D, and this deficiency has been associated with disease severity and hepatic fibrosis.340–345 Vitamin D protects against oxidative stress, limits the proliferation of myofibroblasts, stimulates the expansion of regulatory T cells, reduces the production of pro-inflammatory cytokines, and modulates activation of immune effector cells.346–348 Low serum levels of 25-hydroxyvitamin D may compromise these diverse beneficial actions, and vitamin D supplementation may be a measure to bolster actions that protect hepatocytes.349 The impact of supplemental vitamin D therapy on the severity and responsiveness of corticosteroid-treated autoimmune hepatitis also requires evaluation.
Nonclassical Phenotypes of Autoimmune Hepatitis at Presentation
| Nonclassical phenotype | Features | Implications |
|---|---|---|
| Acute onset | Frequency, 25%–75%63,65 Newly developed or exacerbated pre-existent disease61,63 |
Can resemble acute viral, drug-induced, toxic or ischemic injury61 Responds well to standard treatment61,63 |
| Acute severe (fulminant) onset | Frequency, 3%–6%66,67 Onset encephalopathy ≤26 weeks61 Classical features may be absent68 Centrilobular necrosis in 86%67 Lymphoplasmacytic infiltrates and interface hepatitis in 50%–90%67 Heterogeneous hypoattenuated regions by unenhanced CT71 |
Can resemble acute viral, drug-induced, toxic or ischemic injury61 Requires transplantation evaluation61 Variable response to corticosteroids and possible complications (sepsis)61 |
| Asymptomatic presentation | Frequency, 25%–34%72,73 Histological features similar to symptomatic patients73 Become symptomatic in 26%–70%72,73 Survival without treatment possible72 |
Low frequency of resolution if untreated (12% vs 63%)74 Lower 10-year survival if untreated than in treated severe AIH (67% vs 98%)74 Consider treating all patients74 |
| Autoantibody-negative phenotype | Scoring systems diagnostic, 19%–22%75 Acute liver failure possible83,84 Anti-SLA positive in 9%–31%26,83 |
Steroid-responsive, 67%–87%75,81 Test for nonstandard antibodies75 Exclude celiac disease89,90,93 |
| Atypical histological patterns | Centrilobular necrosis in 29%94 Bile duct injury or loss possible100,101 |
May reflect severity and acuity of AIH94 or suggest other diagnoses102 |
| Graft dysfunction posttransplant | Recurrent AIH, 8%–12% after 1st year122 Anti-GSTT1 common in |
Variable steroid response113 Cirrhosis and graft failure possible113 Retransplantation required, 23%–50%113 |
| Overlap syndrome | Mixed features of AIH+PBC or PSC102,107 “Paris criteria” for AIH+PBC105,135 |
Variable treatment response52,53 Frequently treated with steroids+UDCA130 |
CT, computed tomography; AIH, autoimmune hepatitis; anti-SLA, antibodies to soluble liver antigen; anti-GSTT1, antibodies to glutathione-S-transferase T1; PBC, primary biliary cholangitis; PSC, primary sclerosing cholangitis; UDCA, ursodeoxycholic acid.
Comprehensive Diagnostic Scoring System of the International Autoimmune Hepatitis Group
| Clinical features | Points | Clinical features | Points |
|---|---|---|---|
| Female | +2 | Average alcohol intake (g/day) | |
| <25 | +2 | ||
| >60 | −2 | ||
| AP:AST (or ALT) ratio | Histologic findings | ||
| <1.5 | +2 | Interface hepatitis | +3 |
| 1.5–3.0 | 0 | Lymphoplasmacytic infiltrate | +1 |
| >3.0 | −2 | Rosette formation | +1 |
| Biliary changes | −3 | ||
| Other atypical changes | −3 | ||
| None of above | −5 | ||
| Serum globulin or IgG level above ULN | Concurrent immune disease, including celiac disease | +2 | |
| >2.0 | +3 | Other autoantibodies | +2 |
| 1.5–2.0 | +2 | HLA DRB1*03 or DRB1*04 | +1 |
| 1.0–1.5 | +1 | ||
| <1.0 | 0 | ||
| ANA, SMA, or anti-LKM1 | Response to corticosteroids | ||
| >1:80 | +3 | Complete | +2 |
| 1:80 | +2 | Relapse after drug withdrawal | +3 |
| 1:40 | +1 | ||
| <1:40 | 0 | ||
| AMA positive | −4 | ||
| Hepatitis markers | Aggregate score pretreatment | ||
| Positive | −3 | Definite autoimmune hepatitis | >15 |
| Negative | +3 | Probable autoimmune hepatitis | 10–15 |
| Hepatotoxic drug exposure | Aggregate score posttreatment | ||
| Positive | −4 | Definite autoimmune hepatitis | >17 |
| Negative | +1 | Probable autoimmune hepatitis | 12–17 |
AP, alkaline phosphatase; AST, aspartate aminotransferase; ALT, alanine aminotransferase; IgG, immunoglobulin G; ULN, upper limit of the normal range; HLA, human leukocyte antigen; ANA, antinuclear antibodies; SMA, smooth muscle antibodies; anti-LKM1, antibodies to liver kidney microsome type 1; AMA, antimitochondrial antibodies.
Adapted from Alvarez F,
Simplified Diagnostic Scoring System of the International Autoimmune Hepatitis Group
| Category | Scoring elements | Results | Points |
|---|---|---|---|
| Autoantibodies | ANA or SMA | 1:40 by IIF | +1 |
| ANA or SMA | ≥1:80 by IIF | +2 | |
| Anti-LKM1 (alternative to ANA and SMA) | ≥1:40 by IIF | +2 | |
| Anti-SLA (alternative to ANA, SMA and LKM1) | Positive | +2 | |
| Immunoglobulins | Immunoglobulin G level | >ULN | +1 |
| >1.1 times ULN | +2 | ||
| Histological findings | Interface hepatitis | Compatible features | +1 |
| Typical features | +2 | ||
| Viral markers | IgM anti-HAV, HBsAg, HBV DNA, HCV RNA | No viral markers | +2 |
| Probable diagnosis | ≥6 | ||
| Definite diagnosis | ≥7 |
ANA, antinuclear antibodies; SMA, smooth muscle antibodies; anti-LKM1, antibodies to liver kidney microsome type 1; SLA, soluble liver antigen; IIF, indirect immunofluorescence; ULN, upper limit of the normal range; IgM, immunoglobulin M; HAV, hepatitis A virus; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; DNA, deoxyribonucleic acid; HCV, hepatitis C virus; RNA, ribonucleic acid.
Adapted from Hennes EM,
Standard Antibodies for the Diagnosis of Autoimmune Hepatitis
| Standard antibodies | Antigenic target(s) | Clinical features |
|---|---|---|
| ANA | Centromere, ribonucleoproteins, ribonucleoprotein complexes, histones160,161 | Lacks organ and disease specificity156 |
| Present in 80% of adults with AIH156 | ||
| Occurs in 20%–40% with non-AIH156–158 | ||
| Sensitivity for AIH when isolated finding, 32%156 | ||
| Specificity for AIH when isolated finding, 76%156 | ||
| Diagnostic accuracy for AIH, 56%156 | ||
| Concurrent ANA and SMA most diagnostic (74%)156 | ||
| Titers can vary outside disease activity86,156 | ||
| SMA | Filamentous (F) actin, 86%162 | Lacks organ and disease specificity156 |
| Nonactin components, 14%162 | Present in 63% of adults with AIH156 | |
| Occurs in 3%–16% with non-AIH156–158 | ||
| Sensitivity for AIH when isolated finding, 16%156 | ||
| Specificity for AIH when isolated finding, 96%156 | ||
| Diagnostic accuracy for AIH, 61%156 | ||
| Concurrent SMA and ANA most diagnostic (74%)156 | ||
| Titers >1:80 associated with disease activity159 | ||
| Anti-LKM1 | Cytochrome P450 2D6167,168 | Present in 3% of North American adults with AIH149 |
| Detected in 14%–38% of British children with AIH11,163 | ||
| Occurs in 0%–10% of chronic hepatitis C156,164–166 | ||
| Low concurrence with SMA and ANA, 2%156 | ||
| High specificity (99%), low sensitivity (1%)156 | ||
| Diagnostic accuracy in North American adults, 57%156 |
ANA, antinuclear antibodies; AIH, autoimmune hepatitis; SMA, smooth muscle antibodies; anti-LKM1, antibodies to liver kidney microsome type 1.
Nonstandard Antibodies for the Diagnosis of Autoimmune Hepatitis
| Nonstandard antibodies | Antigenic target(s) | Clinical features |
|---|---|---|
| Antibodies to actin (antiactin) | Filamentous (F) actin162 | Present in 87% with AIH162,170,172 |
| Nonactin components162 | Concurrent with SMA in 86%–100% with AIH162,173 | |
| SMA without antiactin in 14% with AIH162 | ||
| Indirect marker of disease activity159,162 | ||
| No standardized assay162,177 | ||
| Antibodies to α-actinin (anti-α-actinin) | α-Actinin178 | Present in 42% of patients with AIH27 |
| Antiactin+anti-α-actinin associated with severity27 | ||
| Baseline level predictive of treatment response30 | ||
| Investigational assay not generally available27,30 | ||
| Antibodies to soluble liver antigen (anti-SLA) | Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase (SEPSECS)23,182,183 | Present in 7%–22% with AIH26,31,87,179,180 |
| Genetic association with HLA DRB1*030124,25 | ||
| Associated with severity, response, relapse, survival24–26 | ||
| Useful in diagnosing seronegative patients159,180,181 | ||
| Specificity, 99%, and sensitivity, 11%179 | ||
| Atypical perinuclear antineutrophil cytoplasmic antibodies (pANCA) | β-Tubulin isotype 5189 | Cross reacts with precursor bacterial protein (FtsZ)189 |
| Present in 50%–92% with typical AIH88,187–189 | ||
| Absent in anti-LKM1-positive AIH190 | ||
| Detected in CUC, PSC, PBC, minocycline injury188,191,193 | ||
| Useful in classifying seronegative AIH17,76,171,195 | ||
| Antibodies to asialoglycoprotein receptor (anti-ASGPR) | Asialoglycoprotein receptor198,199 | Present in 67%–88% with AIH28,198–201 |
| Occurs in other acute and chronic liver diseases198,203,204 | ||
| Useful in classifying seronegative AIH205 | ||
| Correlates with laboratory and histological activity206 | ||
| May predict relapse and define treatment end points201,206 | ||
| Antibodies to liver cytosol type 1 (anti-LC1) | Formiminotransferase cyclodeaminase219–222 | Present in 24%–32% of anti-LKM1-positive AIH208–210 |
| Occurs in chronic hepatitis C and anti-LKM1211–214 | ||
| Useful in classifying seronegative AIH217,218 | ||
| Rare in North American adults with AIH216 |
AIH, autoimmune hepatitis; SMA, smooth muscle antibodies; HLA, human leukocyte antigen; anti-LKM1, antibodies to liver kidney microsome type 1; CUC, chronic ulcerative colitis; PSC, primary sclerosing cholangitis; PBC, primary biliary cholangitis.
Standard Drug Regimens for Autoimmune Hepatitis
| Clinical situation | Combination therapy | Monotherapy | |
|---|---|---|---|
| Prednisone or prednisolone | Azathioprine | Prednisone or prednisolone | |
| xTreatment-naïve* | 30 mg daily×1 wk17,18,34 | 50 mg daily fixed dose17,18,34 | 60 mg daily×1 wk17,18,34 |
| 20 mg daily×1 wk | 40 mg daily×1 wk | ||
| 15 mg daily×2 wk | 30 mg daily×2 wk | ||
| 10 mg daily maintenance | 20 mg daily maintenance | ||
| Treatment failure | 30 mg daily×1 mo253,256 | 150 mg daily×1 mo253,256 | 60 mg daily×1 mo253,256 |
| 20 mg daily×1 mo if improved | 100 mg daily×1 mo if improved | Reduce dose by 10 mg for each month of improvement until 20 mg daily maintenance | |
| 10 daily maintenance if improvement continues | 50 mg daily maintenance if improvement continues | ||
| Increase dose to last level of improvement×1 mo if worsens | Increase dose to last level of improvement×1 mo if worsens | Increase dose to last level of improvement×1 mo if worsens | |
| Increase to 30 mg daily if worsening continues | Increase to 150 mg daily if worsening continues | Increase to 60 mg daily if worsening continues | |
| Incomplete response | 10 mg daily253 | 2 mg/kg daily253 | 20 mg daily253 |
| Dose reductions to maintain normal or near-normal liver tests with goal of drug withdrawal | Fixed dose as steroid dose reduced or discontinued with goal of indefinite azathioprine maintenance | Dose reductions to lowest dose possible to maintain normal or near-normal liver tests | |
| Drug intolerance | Decrease dose or discontinue steroid17,253 | Decrease dose or discontinue azathioprine17,253 | Decrease dose or discontinue steroid17,253 |
| Increase azathioprine dose to 100 or 150 mg daily if necessary | Increase dose of steroid as needed or cautiously consider mycophenolate mofetil, 1–2 g daily41,45,46 | Add azathioprine, 50 mg daily, and adjust dose | |
| Relapse after drug withdrawal | Resume original regimen until resolution of liver tests | Resume original regimen until resolution of liver tests | Resume original regimen for until resolution of liver tests |
| Gradually withdraw and discontinue as dose of azathioprine increased17,253 | Increase dose to 2 mg/kg daily and continue indefinitely17,32,253 | Decrease steroid dose to lowest level and maintain indefinitely17,253,259 | |
Treatment-naïve regimens in Europe commonly include prednisolone at 1 mg/kg daily and azathioprine at 1–2 mg/kg daily.33,234,235
Alternative Drug Regimens for Autoimmune Hepatitis
| Clinical situation | Budesonide | Mycophenolate mofetil | Calcineurin inhibitors |
|---|---|---|---|
| Treatment-naïve | 6–9 mg daily combined with azathioprine, 1–2 mg daily44 | 1.5–2 g daily combined with prednisolone, 0.5–1 mg/kg daily47 | Cyclosporine, 2–5 mg/kg daily (trough, 100–300 ng/mL)36 |
| Outcomes in juvenile AIH equivalent to standard therapy266 | No established superiority over standard therapy34 | Tacrolimus, 3 mg twice daily (serum level, 3 ng/mL)35 | |
| Preferred in mild, noncirrhotic, uncomplicated AIH and patients with low steroid tolerance34 | Equivalent to standard combination therapy and not preferred51,274,275 | ||
| Treatment failure | Not effective in limited trial271 | Effective in 23%34,50 | Cyclosporine effective in 93%49 |
| Side effects with cirrhosis268,269 | Avoid in pregnancy and severe cytopenia49,272,273 | Tacrolimus effective in 87%38,276 | |
| Low enthusiasm despite success49,277 | |||
| Drug intolerance | Difficult to switch with prednisone without severe withdrawal symptoms271 | Effective in 58%34,50 | Limited use in steroid intolerance and associated with other complexities36,49 |
| Avoid in pregnancy and severe cytopenia49,272,273 |
AIH, autoimmune hepatitis.
Emerging Molecular, Cellular and Pharmacological Interventions for Autoimmune Hepatitis
| Emerging interventions | Putative actions | Experience |
|---|---|---|
| Molecular interventions | ||
| CTLA-4Ig (abatacept) | Disrupts CD28 binding to B7 ligands52 | Approved for rheumatoid arthritis52 |
| Dampens T lymphocyte activation34,300 | Improved murine model of PBC303 | |
| Anti-CD20 (rituximab) | Inhibits B lymphocyte activation53,300 | Isolated patients with AIH281–284 |
| Effective in refractory AIH285 | ||
| Anti-TNF-α (infliximab) | Inhibits TNF-α and interferes with maturation of cytotoxic T cells34,52 | Effective in refractory AIH55 |
| Frequent side effects (27%)55 | ||
| Nonmitogenic anti-CD3 | Binds to antigen receptor of T cells300 | Effective in diabetic model307 |
| Promotes apoptosis of immune cells34,53 | Increases insulin in diabetic humans308 | |
| Anti-lysyl oxidase-like 2 (simtuzumab) | Inhibits lysyl oxidase and antifibrotic323 | Phase 2 studies to prevent fibrosis in NAFLD and PSC (https://clinicaltrials.gov) |
| Prevents cross-linkage of collagen322 | ||
| Cellular interventions | ||
| Adoptive transfer of regulatory T cells | Corrects deficiencies in cell population60 | Effective in models of AIH56,312 |
| Expands immune regulatory population60 | Effective in model of PBC313 | |
| Adoptive transfer of mesenchymal stromal cells | Affects innate and adaptive immunity60 | Effective in models of RA301 |
| Inhibits B and T lymphocytes60 | Promising in early human studies319–321 | |
| Modulation of natural killer T cells | Tailored glycolipid antigens skew dual immune actions favorably59,314,315 | Effective in animal models of diabetes, RA, SLE and AIH300,316,317 |
| Pharmacological prospects | ||
| Antioxidants (N-acetylcysteine, S-adenosyl-L methionine) | Reduce reactive oxygen species322,323 | Effective in NAFLD, chronic hepatitis C, and alcoholic cirrhosis324–327 |
| Decrease hepatocyte apoptosis322,323 | ||
| Inhibit stellate cell activation322,323 | ||
| Angiotensin inhibitors (losartan) | Reduce profibrotic transformation of hepatic stellate cells to myofibroblasts322 | Decreased fibrosis in chronic hepatitis C328 |
CTLA-4Ig, cytotoxic T lymphocyte antigen-4 fused with human immunoglobulin; PBC, primary biliary cholangitis; AIH, autoimmune hepatitis; TNF-α, tumor necrosis factor-alpha; NAFLD, nonalcoholic fatty liver disease; PSC, primary sclerosing cholangitis; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus.
Gut and Liver 2016; 10(2): 177-203
Published online March 15, 2016 https://doi.org/10.5009/gnl15352
Copyright © Gut and Liver.
Albert J. Czaja
Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, MN, USA
Correspondence to: Albert J. Czaja, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, 200 First Street S.W., Rochester, MN 55905, USA, Tel: +1-507-284-2691, Fax: +1-507-284-0538, E-mail: czaja.albert@mayo.edu
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Autoimmune hepatitis is characterized by autoantibodies, hypergammaglobulinemia, and interface hepatitis on histological examination. The features lack diagnostic specificity, and other diseases that may resemble autoimmune hepatitis must be excluded. The clinical presentation may be acute, acute severe (fulminant), or asymptomatic; conventional autoantibodies may be absent; centrilobular necrosis and bile duct changes may be present; and the disease may occur after liver transplantation or with features that suggest overlapping disorders. The diagnostic criteria have been codified, and diagnostic scoring systems can support clinical judgment. Nonstandard autoantibodies, including antibodies to actin, α-actinin, soluble liver antigen, perinuclear antineutrophil antigen, asialoglycoprotein receptor, and liver cytosol type 1, are tools that can support the diagnosis, especially in patients with atypical features. Prednisone or prednisolone in combination with azathioprine is the preferred treatment, and strategies using these medications in various doses can ameliorate treatment failure, incomplete response, drug intolerance, and relapse after drug withdrawal. Budesonide, mycophenolate mofetil, and calcineurin inhibitors can be considered in selected patients as frontline or salvage therapies. Molecular (recombinant proteins and monoclonal antibodies), cellular (adoptive transfer and antigenic manipulation), and pharmacological (antioxidants, antifibrotics, and antiapoptotic agents) interventions constitute future directions in management. The evolving knowledge of the pathogenic pathways and the advances in technology promise new management algorithms.
Keywords: Diagnosis, Atypical phenotypes, Autoantibodies, Treatment
Autoimmune hepatitis has diverse clinical phenotypes, and this diversity has complicated its diagnosis and management.1–5 The classical perception of autoimmune hepatitis as a chronic inflammatory liver disease that affects mainly young white women has been expanded,6–8 and diagnostic boundaries now encompass patients of both genders9,10 all ages,11–14 and various ethnic groups.5,15 Patients may have acute, acute severe (fulminant), or asymptomatic presentations; they may lack conventional serological markers; and they may have atypical histological features.1–5 Autoimmune hepatitis must now be considered in all patients with acute and chronic hepatitis of undetermined cause, including patients with graft dysfunction after liver transplantation.16–18
Diagnostic criteria have been codified, and diagnostic scoring systems have been developed to supplement clinical judgment in difficult cases.19–21 The repertoire of serological markers has been expanded to improve diagnosis, and investigational assays are evolving that may have prognostic implications.22–31 Corticosteroids alone or in combination with azathioprine are the mainstays of treatment,17,18,32–34 but regimens, involving calcineurin inhibitors, mycophenolate mofetil, and budesonide, have emerged from diverse clinical experiences as alternative front-line and salvage therapies.35–51 Furthermore, the clarification of pathogenic molecular and cellular interactions have suggested new, testable, therapeutic interventions.34,52–60
The goals of this review are to describe the nonclassical clinical phenotypes of autoimmune hepatitis, present the diagnostic criteria that have been formalized for this disease, indicate the current and evolving serological repertoire, present guidelines for the administration of conventional treatment regimens, outline strategies for incorporating nonstandard drugs in the treatment of selected patients, and indicate the site-specific molecular, cellular and pharmacological interventions that constitute future directions in the management of this disease.
An acute presentation occurs in 25% to 75% of patients with autoimmune hepatitis,61–65 and an acute severe (fulminant) presentation, characterized by the development of hepatic encephalopathy within 26 weeks of disease discovery, occurs in 3% to 6% of North American and European patients (Table 1).66,67 Each presentation can suggest an acute viral, toxic, or drug-induced liver injury, and each can delay recognition and proper treatment of autoimmune hepatitis.
Classical features of autoimmune hepatitis may be absent or less evident in patients with an acute severe (fulminant) presentation. Antinuclear antibodies (ANA) are undetected or weakly positive in 29% to 39% of patients,68,69 and serum immunoglobulin G (IgG) levels are normal in 25% to 39% of individuals (Table 1).25,69 Centrilobular hemorrhagic necrosis and massive or submassive liver necrosis dominate the histological findings in 86% of patients.67,68
Central perivenulitis with a prominent lymphoplasmacytic infiltrate and interface hepatitis supports the diagnosis of autoimmune hepatitis in 50% to 90% of patients with acute liver failure,67 and a histological assessment has been encouraged if liver tissue can be obtained safely.69,70 Heterogeneous hypoattenuated regions within the liver can be demonstrated by unenhanced computed tomography in 65% of patients with autoimmune hepatitis and acute liver failure, and these findings are disease-specific.61,71
Autoimmune hepatitis is asymptomatic in 25% to 34% of patients, and the diagnosis must be considered in all individuals with newly discovered mild liver test abnormalities (Table 1).72,73 Symptoms develop in 26% to 70% of patients within 2 to 120 months (mean interval, 32 months), and histological findings, including the frequencies of moderate to severe interface hepatitis (87% vs 93%), periportal fibrosis (41% vs 41%), and bridging fibrosis (39% vs 48%), are similar between asymptomatic and symptomatic individuals.73
Untreated patients with mild, asymptomatic, autoimmune hepatitis improve spontaneously less frequently (12% vs 63%, p=0.006) and less completely than treated patients with severe symptomatic disease during 77±31 months of observation,74 and they have a lower 10-year survival (67% vs 98%, p=0.01).74 The uncertainty that mild autoimmune hepatitis remains mild compels the consideration of corticosteroid therapy in all patients with the diagnosis.
Patients with typical clinical and laboratory findings of autoimmune hepatitis may lack ANA, smooth muscle antibodies (SMA), and antibodies to liver kidney microsome type 1 (anti-LKM1) (Table 1).75–77 The revised original scoring system of the International Autoimmune Hepatitis Group (IAIHG) has reclassified 34% of patients with cryptogenic chronic hepatitis as definite or probable autoimmune hepatitis in one European study,78 and two North American studies have indicated that 19% to 22% of patients with cryptogenic hepatitis can be categorized as autoimmune hepatitis by the scoring system of the IAIHG79 or by clinical judgment.80 Lower frequencies of autoantibody-negative autoimmune hepatitis (1% to 5%) have been reported in other studies applying different diagnostic criteria.81,82 Auto-antibody-negative autoimmune hepatitis has been a cause of acute liver failure in 7% of British patients83 and 24% of Japanese patients with acute severe (fulminant) presentations.84
Antinuclear antibodies and SMA may emerge later in the course of the disease;85,86 or nonstandard autoantibodies may be detected and support the diagnosis.75 Antibodies to soluble liver antigen (anti-SLA) occur in 9% to 31% of these patients;26,83,87 atypical perinuclear antineutrophil cytoplasmic antibodies (pANCA) support the diagnosis in some patients;88 and immunoglobulin A (IgA) antibodies to tissue transglutaminase or endomysium may implicate celiac disease as the basis for the liver dysfunction in other patients.89–93 The absence of autoantibodies does not preclude the diagnosis of autoimmune hepatitis or a benefit from corticosteroid therapy.75,76,81
Interface hepatitis is the
Bile duct injury may also be present with interface hepatitis.98–100 Biliary lesions that are isolated, unassociated with a cholestatic clinical syndrome, and unaccompanied by antimitochondrial antibodies (AMA) may constitute AMA-negative primary biliary cholangitis (PBC) or small duct primary sclerosing cholangitis (PSC).100–104 Bile duct injury, including destructive cholangitis (florid duct lesions), in conjunction with AMA in patients with otherwise classical features of autoimmune hepatitis may constitute an overlap syndrome between autoimmune hepatitis and PBC.102,105–107 Bile duct injury manifested by ductopenia, portal fibrosis, and portal edema suggests an overlap syndrome with PSC.102
Autoimmune hepatitis can recur or develop
Diagnostic criteria for recurrent or
Patients with autoimmune hepatitis and features classically associated with PBC (AMA and histological features of bile duct injury or loss) and PSC (absence of AMA and cholangiographic changes of focal biliary strictures and dilations) have an overlap syndrome (Table 1).106,129,130 Patients with autoimmune hepatitis may also have a cholestatic syndrome in the absence of classical features of PBC and PSC.99 These patients may have an overlap syndrome with AMA-negative PBC or small duct PSC.102,103,107
The overlap syndromes occur in approximately 10% of patients with otherwise classical features of autoimmune hepatitis.107 The major clinical consequence of the overlap syndromes is a variable response to conventional treatment regimens, and for this reason the diagnosis should be considered in all patients with refractory autoimmune hepatitis.106 Treatment is empiric and based on weak clinical evidence. Corticosteroids in combination with low dose ursodeoxycholic acid (13 to 15 mg/kg daily) is a common management strategy endorsed by the major liver societies.105,130–132
The gold standard for the diagnosis is clinical judgment, and the strongest independent predictor of an overlap syndrome is the liver tissue examination.133,134 The “Paris criteria” provide an objective basis for diagnosing the overlap syndrome between autoimmune hepatitis and PBC,105 and they have a sensitivity of 92% and specificity of 97% compared to clinical judgment.135
Formalized diagnostic criteria ensure the application of a standardized diagnostic algorithm,19 and diagnostic scoring systems provide an evaluation template that can support the diagnosis in difficult cases.19–21 All diagnostic guidelines recommend the performance of a liver tissue examination to establish the diagnosis.17,19,33,136 Retrospective studies that propose elimination of the diagnostic tissue examination have failed to evaluate its importance in excluding patients with similar features but other diagnoses.137,138
The diagnostic criteria of the IAIHG require the presence of compatible laboratory (serum aspartate [AST] and alanine aminotransferase [ALT] abnormalities, hypergammaglobulinemia, and increased serum IgG level), serological (ANA, SMA or anti-LKM1 positivity) and histological findings (interface hepatitis with or without plasma cell infiltration).19 Diseases that can resemble autoimmune hepatitis must also be excluded by appropriate tests, and these include virus-related, drug-induced, alcoholic, hereditary (Wilson disease, hereditary hemochromatosis), metabolic (nonalcoholic fatty liver disease [NAFLD]), and immune-mediated cholestatic diseases (PBC and PSC).19 The designation of definite or probable autoimmune hepatitis reflects the level of confidence in the diagnosis based on the compatibility of the clinical features with classical autoimmune hepatitis. Two scoring systems are available for challenging cases.19,20
The revised original scoring system is a comprehensive template that evaluates 13 clinical categories and renders 27 possible grades (Table 2).19 This comprehensive scoring system was originally developed as a research tool by which to ensure the homogeneity of patient populations in clinical studies.139 It has emerged subsequently as a template by which to ensure the systematic evaluation of patients, and it can serve as a mechanism by which to bolster clinical judgment.21,140 The scoring system can accommodate deficiencies or inconsistencies in the clinical presentation and support the diagnosis in difficult cases by rendering a composite score before and after corticosteroid treatment.
A simplified scoring system has been developed to ease clinical application.20 It evaluates four clinical categories and renders nine possible grades (Table 3).20 The original revised scoring system has greater sensitivity for autoimmune hepatitis (100% vs 95%),21 whereas the simplified scoring system has superior specificity (90% vs 73%) and accuracy (92% vs 82%), using clinical judgment as the gold standard.21 The simplified scoring system does not grade the treatment response, and this difference may contribute to its lower sensitivity.141 The revised original scoring system reclassifies patients with cryptogenic hepatitis as autoimmune hepatitis more commonly than the simplified scoring system (95% vs 24%), whereas the simplified scoring system excludes the diagnosis of autoimmune hepatitis more frequently in liver diseases that have concurrent immune manifestations (83% vs 64%).21
The diagnostic scoring systems have been extensively evaluated and refined by retrospective analyses of patients that have been characterized in single medical centers and diagnosed by experts in autoimmune liver disease.20,21,140–143 These characterizations have not followed a predefined protocol; pooled experiences have been limited; and comparative studies between medical centers have not been performed.141 Furthermore, assessments have not always been uniform or complete in each patient.20 Collaborative prospective clinical studies that adhere to a pre-established protocol and that ensure a uniform and complete assessment of each patient are necessary to validate the scoring systems.
The scoring systems have been applied beyond their original design and intention. They have been used inappropriately to determine the presence of autoimmune hepatitis in patients with PBC,144–146 and this application has been discouraged.130 The scoring systems have also been used but not validated in patients with acute severe (fulminant) liver failure141,147 and in patients with graft dysfunction after liver transplantation.113
The performance parameters of the revised original and simplified scoring systems for autoimmune hepatitis are based on their compatibility with the gold standard of clinical judgment.19–21,140 The results of these scoring systems can never supersede clinical judgment, and they cannot make a clinically untenable diagnosis tenable. Misapplication of the scoring systems and overinterpretation of their results are major pitfalls that must be avoided.
Antinuclear antibodies, SMA, and anti-LKM1 characterize most patients with autoimmune hepatitis, and they should be assessed in all candidates for the diagnosis (Table 4).17 Antinuclear antibodies and SMA are usually present in the absence of anti-LKM1, and anti-LKM1 are usually detected in the absence of ANA and SMA.148,149 This exclusivity has justified the designations of type 1 autoimmune hepatitis for those patients with ANA and/or SMA, and type 2 autoimmune hepatitis for those patients with anti-LKM1.148
The subtypes of autoimmune hepatitis have been associated with different age groups148 and genetic predispositions,150–153 but they have not been associated with major differences in treatment outcomes.17,33,154 Accordingly, the subtypes have not been endorsed as valid pathological entities. Indeed, among adults with autoimmune hepatitis, there have been no significant clinical, laboratory, histological, genetic or outcome differences to justify a designation of type 1 and type 2 autoimmune hepatitis.155
Antinuclear antibodies and SMA lack disease- and organ-specificity (Table 4). Antinuclear antibodies are present in 80% of patients with autoimmune hepatitis, and SMA occur in 63%.156 These antibodies also occur commonly in other liver diseases. Antinuclear antibodies are present in 20% to 40% of patients with alcoholic liver disease, NAFLD, chronic viral hepatitis, PBC or PSC.156–158 Smooth muscle antibodies occur in 3% to 16% of patients with alcoholic liver disease, NAFLD, chronic hepatitis C, PBC or PSC.156–158 Each autoantibody has low sensitivity for the diagnosis (32% for ANA and 16% for SMA) when present as an isolated finding.156 The performance parameters of ANA and SMA are enhanced if both autoantibodies are present. The concurrence of ANA and SMA has a sensitivity of 43%, specificity of 99%, and diagnostic accuracy of 74% for autoimmune hepatitis.156
Antinuclear antibodies seem to be the most variable marker during the course of the disease,86 whereas SMA in titers >1:80 are associated with laboratory (77%) and histological (100%) activity.159 Antinuclear antibodies are reactive against multiple nuclear components, including centromere, ribonucleoproteins, ribonucleoprotein complexes and histones, and 46% of patients with ANA have multiple nuclear reactivities.160,161 Smooth muscle antibodies in autoimmune hepatitis are directed mainly against filamentous (F) actin, but nonactin reactivities are present in 14% of patients with SMA.162
Antibodies to LKM1 are present in 3% of North American adults149,156 and 14% to 38% of British children with autoimmune hepatitis (Table 4).11,163 They can also be demonstrated in 0% to 2% of North American patients156,164 and 10% of European patients with chronic hepatitis C.165,166 Antibodies to LKM1 have a sensitivity of only 1% for autoimmune hepatitis in North American adults, but their specificity is 99% and their diagnostic accuracy is 57%. Only 2% of patients with ANA or SMA have anti-LKM1.156 The cytochrome mono-oxygenase, P450 2D6, is the target antigen of anti-LKM1.167,168
The nonstandard autoantibodies constitute a repertoire of serological markers that can support or extend the diagnosis of autoimmune hepatitis to highly selected individuals in whom the standard biomarkers are insufficient to render a diagnosis.169–171 The presence of nonstandard autoantibodies can upgrade the diagnosis of autoimmune hepatitis by the revised original diagnostic scoring system of the IAIHG.17,19
Antibodies to actin (antiactin) are directed against filamentous (F) actin, and they are present in 87% of patients with autoimmune hepatitis (Table 5).162,170,172 They also occur in diverse immune-mediated, nonliver diseases, including systemic lupus erythematosus, Sjögren syndrome, rheumatoid arthritis, celiac disease, diabetes, autoimmune thyroiditis and Crohn’s disease.170 Antibodies to actin are a subset of SMA, and 86% to 100% of patients with autoimmune hepatitis and SMA have antiactin.162,173 Both SMA and antiactin are indirect markers of laboratory and histological activity in autoimmune hepatitis.159
Most patients with antiactin have at least SMA or other conventional autoantibodies, and the detection of antiactin is not critical for the diagnosis.162 Antibodies to actin have been associated with a higher frequency of death from hepatic failure or requirement for liver transplantation, but the prognostic implications of these antibodies are assay dependent.27,30,162,173–176 Multiple assays for antiactin are available, but none has been incorporated into a standard diagnostic repertoire.162,177
α-Actinins are cross-linking proteins that bind to actin and that are expressed as isoforms in muscle and nonmuscle cells.178 Antibodies to α-actinin have been found by enzyme-linked immunosorbent assay (ELISA) in 42% of patients with autoimmune hepatitis compared to 13% of patients with other liver diseases and 6% of healthy blood donors (Table 5).27 Antibodies to α-actinin are present in 66% of patients with autoimmune hepatitis who are positive for antifilamentous actin (anti-F actin), and the combination seems to be specific for the disease.27
Double reactivity to anti-F-actin and anti-α-actinin seems to have prognostic implications. Patients with both antibodies have clinical and histological activity and a severe form of the disease characterized by an acute onset.27 Patients who respond to corticosteroid regimens have lower baseline levels of anti-α-actinin than patients who relapse or respond incompletely, and the baseline level of anti-α-actinin has been an independent predictor of treatment response.30 The assay for anti-α-actinin is still investigational and not generally available.27,30
Antibodies to soluble liver antigen (anti-SLA) are present in 7% to 22% of patients with autoimmune hepatitis, and their occurrence varies among different ethnic groups (Table 5).26,31,87,179,180 Antibodies to soluble liver antigen seem to be least common in Japanese patients (7%)26 and most common in German patients (19% to 22%).26,87 The variability in serological expression may have a genetic basis, and anti-SLA have been associated with human leukocyte antigen (HLA) A1-B8 in Germany87 and HLA DRB*0301 in Britain25 and the United States.24
Antibodies to soluble liver antigen have high specificity for autoimmune hepatitis (99%),179 and they have been the sole marker of autoimmune hepatitis in 14% to 20% of patients who would otherwise have been classified as cryptogenic hepatitis.159,180,181 They also have been associated with more severe histological findings, longer treatment requirement to suppress inflammatory activity, increased frequency of relapse after drug withdrawal, and higher frequency of liver transplantation or death from liver failure than patients without this marker.24–26,87,179 The target antigen of anti-SLA is a transfer ribonucleic acid (RNA)-protein complex, now designated as SEPSECS (Sep [O-phosphoserine] tRNA:Sec [selenocysteine] tRNA synthase).23,182,183 Antibodies to soluble liver antigen have also been closely associated with antibodies to ribonucleoprotein/Sjögren syndrome A antigen (anti-Ro/SSA), and the clinical implications of this tightly linked expression (96% concurrence) remains unclear.31,184–186
Atypical pANCA are detected in 50% to 92% of patients with autoimmune hepatitis, often in high titer (mean titer, 11,410±1,875),88,187–189 and serum titers are not associated with laboratory tests of disease activity (serum AST, IgG, and γ-globulin levels).88 Atypical pANCA exhibit some selectivity in that they are absent in anti-LKM1-positive autoimmune hepatitis,190 but they can occur in chronic ulcerative colitis, PSC, PBC, chronic hepatitis C, and minocycline-induced autoimmune disease.187,188,191–193
The primary target antigen has been characterized as a 50 kDa protein on the inner side of the nuclear envelope,191 and it has been identified as β-tubulin isotype 5.189 Ninety-seven percent of patients with pANCA and autoimmune hepatitis have atypical pANCA, and 88% of the pANCA-positive patients have reactivity to β-tubulin isotype 5.189 The pANCA of autoimmune hepatitis also cross-react with an evolutionary precursor bacterial protein, FtsZ, and 82% of pANCA-positive patients with autoimmune hepatitis have reactivity to both proteins.189 These dual reactivities have justified speculation that intestinal micro-organisms trigger an immune response that results in liver inflammation in genetically susceptible individuals.189,194
The assessment of atypical pANCA has been included in the comprehensive diagnostic scoring system for autoimmune hepatitis,19 and the autoantibodies may be useful in developing the diagnosis of autoimmune hepatitis in patients who are otherwise seronegative and classified as cryptogenic chronic hepatitis.17,76,171,195 The presence of atypical pANCA has been associated with cirrhosis187 and relapse after corticosteroid withdrawal in autoimmune hepatitis,196 but the prognostic implications of atypical pANCA in autoimmune hepatitis have not been sufficiently established to warrant their routine assessment.17,88,197
Antibodies to the asialoglycoprotein receptor (anti-ASGPR) are present in 67% to 88% of patients with autoimmune hepatitis (Table 5).28,198–201 They occur in adults and children with autoimmune hepatitis, and they do not have an exclusive serological profile.202 Antibodies to the asialoglycoprotein receptor can be present in acute hepatitis A (57%), acute hepatitis B (35%), PBC (14% to 100%), chronic hepatitis C (14%), alcoholic liver disease (8%), and chronic hepatitis B (7%).28,198,199,203,204 The lack of disease specificity has compromised the diagnostic function of anti-ASGPR, and the major value of this serological marker may be in the assessment of patients who are seronegative for the conventional markers of autoimmune hepatitis.205
Antibodies to asialoglycoprotein receptor can disappear during corticosteroid therapy, and the disappearance has been associated with histological resolution.206 Patients with anti-ASGPR during corticosteroid therapy also have a higher frequency of relapse after drug withdrawal than patients in whom anti-ASGPR has disappeared or never been expressed (88% vs 33%, p=0.01).201,206 These attributes suggest that anti-ASGPR may be useful in defining end points of treatment.28 The inability to standardize the assay for anti-ASGPR has been the major limitation to its broad clinical application.28,199,201,207
Antibodies to liver cytosol type 1 (anti-LC1) co-exist with anti-LKM1 in 24% to 32% of patients with anti-LKM1-positive au-toimmune hepatitis (Table 5).208–210 They are also present in 12% to 33% of patients with chronic hepatitis C and anti-LKM1,211–214 and they occur infrequently in patients with autoimmune hepatitis and SMA and/or ANA.215 Antibodies to liver cytosol type 1 occur mainly in European children and young adults aged ≤20 years,209,210 and they are rarely found in white North American adults.216 Antibodies to liver cytosol type 1 may be the sole markers of autoimmune hepatitis in patients seronegative for SMA, ANA, and anti-LKM1,217,218 but this diagnostic role may be limited, especially in North American adults in whom the frequency of anti-LC1 has been low.216 Formiminotransferase cyclodeaminase is a cytosolic enzyme that has been identified as the target antigen of anti-LC1.219–222
Prednisone or prednisolone alone or in combination with azathioprine is the mainstay therapy of autoimmune hepatitis (Table 6).17,33 Combination therapy is preferred as lower doses of corticosteroid can be administered when combined with azathioprine, and the frequency of corticosteroid-related side effects is lower (10% vs 44%).223 Both regimens have otherwise similar outcomes.223 All patients with active autoimmune hepatitis are candidates for treatment regardless of symptom status (symptomatic versus asymptomatic) or disease severity (mild versus severe).34,74
Combination therapy is appropriate for most patients, especially those with an anticipated low tolerance for corticosteroids (individuals with obesity, diabetes, hypertension, osteopenia, or emotional instability).34 Monotherapy with corticosteroids is appropriate for patients with a known or anticipated intolerance of azathioprine (individuals with severe cytopenia [leukocyte count, <2.5×109/L; platelet count, <50×109/L], thiopurine methyltransferase deficiency [TPMT], or pregnancy) and for patients with acute severe autoimmune hepatitis or manifestations of acute liver failure.34
The immunosuppressive actions of azathioprine develop slowly over a 6-week period,224,225 and monotherapy with prednisone or prednisolone may have a more rapid action than combination therapy in patients with acute severe disease.49 Azathioprine is a category D drug for pregnancy in the United States, and congenital malformations have occurred in animal studies.226 Furthermore, azathioprine metabolites can pass the human placenta,227 and the drug has been of concern in the occurrence of human fetal complications.228 These concerns have been strongly counterbalanced by numerous studies in azathioprine-treated women with inflammatory bowel disease in whom the rarity or nonexistence of azathioprine-related fetal complications has been documented.184,229–233 Importantly, azathioprine is not an essential drug in the management of autoimmune hepatitis during pregnancy, and the drug can be replaced in pregnancy by an adjusted dose of prednisone or prednisolone.17,138
The preferred treatment regimen combining corticosteroids and azathioprine consists of an induction phase and a maintenance phase (Table 6).34 During the 4-week induction phase, prednisone or prednisolone, 30 mg daily, is administered for 1 week. The dose is then reduced to 20 mg daily for 1 week and 15 mg daily for 2 weeks. Azathioprine, 50 mg daily, is given as a fixed dose during the entire induction phase. After 4 weeks of induction, the dose of prednisone or prednisolone is adjusted to 10 mg daily. The dose of azathioprine is maintained at 50 mg daily. The maintenance phase is continued at fixed doses of prednisone or prednisolone, 10 mg daily, and azathioprine, 50 mg daily, until normalization of serum AST, ALT, bilirubin, and γ-globulin or IgG levels and resolution of the histological abnormalities.17 In Europe, prednisolone is preferred over prednisone, and it is commonly administered in a weight-based dose (up to 1 mg/kg daily) during the induction phase. Similarly, the dose of azathioprine is commonly weight-based (1 to 2 mg/kg daily).33,234,235
Blood leukocyte and platelet counts must be monitored throughout the induction and maintenance phases at 3 to 6 month intervals.17 Progressive cytopenia warrants the reduction or discontinuation of azathioprine. The determination of TPMT activity prior to treatment can identify the 0.3% of the normal population with absent TPMT activity.236 These patients are at risk for azathioprine-induced myelosuppression.138,237 Routine genotyping or phenotyping for TPMT activity has not correlated closely with the occurrence of azathioprine toxicity except in those patients with absent enzyme.238–240 Close monitoring of the clinical and hematological findings has been emphasized for all patients receiving this medication.17
Monotherapy with prednisone or prednisolone involves a 4-week induction phase and then a fixed-dose maintenance phase (Table 6).17 During the 4-week induction phase, prednisone or prednisolone, 60 mg daily, is administered for 1 week. The dose is then reduced to 40 mg daily for 1 week and 30 mg daily for 2 weeks.34 After 4 weeks of induction, the dose of prednisone or prednisolone is reduced to 20 mg daily, and the regimen is maintained until resolution of clinical, laboratory and histological findings.34 An adjuvant program of regular weight-bearing exercise, vitamin D and calcium supplementation, and treatment with bisphosphonates (if justified by bone densitometry or clinical history of bone disease) may protect against progressive corticosteroid-related osteopenia.17
Treatment is continued until normal laboratory tests and liver tissue.17 Normal liver tests are achieved in 66% to 91% of patients within 2 years.138,235,241 The average treatment duration until normal liver tests and normal or near-normal liver tissue is 22 months. Treatment may be extended for ≥3 years, but the frequency of remission decreases to 14% and progression to cirrhosis (54% vs 18%, p=0.03) and need for liver transplantation (15% vs 2%, p=0.048) increases compared to patients who respond fully within 12 months.242
In Europe, treatment is usually continued for at least 2 years before any decision regarding the discontinuation of therapy.235 Histological improvement commonly lags behind clinical and laboratory improvement by 3 to 8 months, and treatment should be continued beyond laboratory resolution before any attempt at drug withdrawal.243 Liver tissue examination is the preferred method of documenting histological resolution, but stable normal laboratory tests for 12 to 18 months may be sufficient to indicate the absence of histological activity and justify the termination of treatment.33
The decision to discontinue therapy must balance the possibility of a sustained long-term drug-free remission against the risk of relapse and the need for retreatment.244 The frequency of achieving a treatment-free state is 19% to 40% in studies of at least 3 years duration80,245–248 and 36% in studies of at least 5 years duration.248 The frequency of relapse after drug withdrawal is 50% to 87% depending on duration of follow-up.246,249,250 Relapse has been associated with progressive hepatic fibrosis in 10% and clinical deterioration in 3%, but in most instances relapse can be effectively treated with the prompt resumption of treatment.251
Ultimately, the decision to stop treatment must be based on patient preferences and the physician’s ability to monitor for relapse and promptly restart treatment if necessary.244 Drug withdrawal can be attempted under close monitoring, and the original treatment regimen can be rapidly resumed if serum aminotransferase levels increase. A rapid and complete response to retreatment can be anticipated (Table 6).249 A long term maintenance regimen can then be instituted after normalization of liver tests by increasing the dose of azathioprine to 2 mg/kg daily and gradually withdrawing the corticosteroid.17,32
Liver tests worsen during therapy (treatment failure) in 7% of patients,252 and they improve but not to normal levels (incomplete response) in 14%.242,253 Treatment-ending side effects associated with corticosteroid therapy occur in 12% to 29%, and they are mainly intolerable cosmetic changes, obesity, emotional instability, and vertebral compression.74,245,254 Treatment ending side effects associated with azathioprine therapy occur in 5% to 10% of patients, and they are mainly nausea, vomiting, rash, cytopenia (≤6%), pancreatitis, and liver toxicity.223,254,255 Patients with cirrhosis develop corticosteroid-induced side effects more commonly than patients without cirrhosis (25% vs 8%) presumably because of increased systemic levels of unbound (free) prednisolone,48,223 and they develop cytopenia that can suggest azathioprine toxicity more often (70% vs 26%, p<0.0001).239,240
Patients who fail conventional treatment are treated with high doses of the original medication (Table 6). The dose of prednisone or prednisolone is increased to 30 mg daily and the dose of azathioprine is increased to 150 mg daily.18,34,39,253,256 Patients receiving monotherapy are treated with prednisone or prednisolone, 60 mg daily. Treatment is continued at a fixed dose for one month. Thereafter, the doses of medication are reduced by 10 mg of prednisone or prednisolone and 50 mg of azathioprine after each month of laboratory and clinical improvement until conventional maintenance levels for that particular regimen are reached.
The inability to improve tests after 1 month justifies continuation of the medication in unaltered dose. Worsening of clinical or laboratory status after a dose reduction warrants an increase in the dose to the last level associated with improvement, and the regimen should be maintained for another month until an improvement warrants another attempt at dose reduction. Clinical and laboratory features improve in 70% to 100% of patients; laboratory resolution occurs in 35%; and treatment withdrawal is possible in 20% to 35%.39,257 Most patients remain on therapy indefinitely, and they are at risk for progression of their liver disease and the development of treatment-related side effects. Refractory progressive disease and manifestations of liver failure compel an evaluation for liver transplantation.
Patients who have not achieved clinical, laboratory and histological normality after 36 months of conventional treatment can be classified as having an incomplete response.242 They are unlikely to achieve complete resolution with additional treatment, and the risk of drug-induced side effects increases. Management can be adjusted to prevent progression of the disease with the lowest tolerated dose of medication possible (Table 6). Therapy with prednisone or prednisolone, 10 mg daily, in combination with azathioprine, 2 mg/kg daily, can be started, and the doses can be gradually decreased to maintain a normal or near-normal serum AST level.253 Treatment is indefinite, and the final regimen may consist of low dose corticosteroid in combination with azathioprine or monotherapy with dose-adjusted azathioprine or corticosteroid.32,258,259
Patients with drug-intolerance are treated by decreasing the dose of the toxic medication or discontinuing its use (Table 6).17,253 The dose of the tolerated medication can be adjusted to suppress inflammatory activity. Mycophenolate mofetil (1 to 2 g daily) has been used for azathioprine intolerance, and it has successfully replaced azathioprine in 58% of cases.41,45,46,49,50 Mycophenolate mofetil has side effects in 3% to 34% of patients, including cytopenia, which may resemble those of azathioprine, and it should be administered with caution or avoided in cytopenic patients.49,260,261 It also has well documented teratogenic effects that preclude its use in pregnancy.262–265
Budesonide, mycophenolate mofetil, and the calcineurin inhibitors (cyclosporine and tacrolimus) have been used as alternative frontline and salvage therapies in autoimmune hepatitis.34 Budesonide has emerged mainly as an alternative frontline therapy in selected patients, whereas mycophenolate mofetil and the calcineurin inhibitors have been used mainly as salvage therapies.34
Budesonide (6 to 9 mg daily) in combination with azathioprine (1 to 2 mg/kg daily) has been shown by randomized clinical trial to normalize serum AST and ALT levels more frequently (47% vs 18%) and with fewer side effects (28% vs 53%) than conventional combination therapy with prednisone (40 mg daily tapered to 10 mg daily) and azathioprine (1 to 2 mg/kg daily) when administered for 6 months (Table 7).44 The histological response has not been documented; the durability of the response is unclear; and the low frequency of laboratory response (18%) and high frequency of side effects (53%) in the patients receiving conventional corticosteroid therapy are unexplained. Nevertheless, budesonide, a next generation glucocorticoid, in combination with azathioprine has emerged as an alternative frontline treatment for autoimmune hepatitis.34
Subset analyses of children randomized to each regimen have disclosed similar frequencies of laboratory resolution (16% vs 15%) and side effects (47% vs 63%) between the budesonide and standard regimens.266 For this reason, the superiority of budesonide therapy over standard treatment to induce remission in juvenile patients has been questioned.267 These observations indicate that budesonide therapy can have variable effects in different populations and that careful patient selection may be the key determinant of outcome.
Therapy with budesonide has been associated with the development of corticosteroid-induced complications in patients with cirrhosis,268,269 break-through exacerbations of the liver disease during treatment that have required standard therapy,270 and severe arthralgias and myalgias in patients previously treated with prednisone that have justified readministration of the standard drug regimen.271 Combination therapy with budesonide and azathioprine may be most appropriate in treatment-naïve patients with mild liver inflammation, early stage disease, and absence of concurrent immune diseases. The presence of obesity, diabetes, hypertension, or osteopenia that might be worsened by prednisone treatment also support consideration of the budesonide regimen.34
Mycophenolate mofetil, a next generation purine antagonist, has been used as a frontline and salvage therapy for autoimmune hepatitis.34 As a frontline treatment in 59 patients treated for 3 to 92 months (mean, 26 months), mycophenolate mofetil (1 g daily adjusted to a final dose of 1.5 to 2 g daily) in combination with prednisolone (0.5 to 1 mg/kg daily followed by a tapered withdrawal) normalized serum ALT and γ-globulin levels in 88%, induced a partial laboratory improvement in 12%, allowed the withdrawal of corticosteroids in 58%, and induced treatment-ending side effects in 3% (Table 7).47 Therapy with mycophenolate mofetil and prednisolone can be effective and safe in treatment-naïve patients, but comparative clinical trials with standard therapy are necessary to establish its preference.
Mycophenolate mofetil has also been used as a salvage therapy for patients with corticosteroid-refractory liver disease or azathioprine intolerance.34 Composite analysis of the several, small, single center experiences indicates that mycophenolate mofetil can induce improvement of laboratory tests in 45%, facilitate the withdrawal of corticosteroids in 40%, and cause treatment-ending side effects in 15% (Table 7).34,50 Outcomes can be improved by using the treatment in a selective fashion. Therapy with mycophenolate mofetil has rescued patients who are azathioprine intolerant more commonly than patients who are refractory to conventional corticosteroid treatment (58% vs 23%),34,41,45,46,50 whereas children with autoimmune hepatitis and sclerosing cholangitis have not responded.
Caveats that must be considered before instituting therapy include recognition than the drug is 6 to 7 times more expensive than azathioprine, treatment is commonly indefinite, side effects develop in 3% to 34%, and pregnancy is an absolute contraindication to its use.49,272,273
Cyclosporine has been used successfully as a frontline agent in children and adults with autoimmune hepatitis,36,274,275 but the only randomized clinical trial involving 39 patients has indicated equivalency rather than superiority of cyclosporine therapy to standard combination therapy (Table 7).51 In the absence of clear advantages that outweigh the risks of treatment (hypertension, nephrotoxicity, infection, pancreatitis, neurotoxicity and malignancy) and its expense, frontline therapy with cyclosporine cannot be justified.49 Similarly, tacrolimus (3 mg twice daily) has also had success as a frontline treatment in 21 patients who improved their serum ALT and AST levels after 3 months.35 The cytopenia and nephrotoxicity that developed in these patients were not treatment-ending, but validation of this regimen by randomized clinical trial has not emerged after 20 years.
The calcineurin inhibitors have also been used successfully to salvage patients with corticosteroid-refractory autoimmune hepatitis.34 Composite clinical experiences with cyclosporine in 22 such patients have indicated improvement of variable degree in 93% and failure of response due to recalcitrance, drug toxicity, or noncompliance in 7%.49,50 Similarly, composite experiences with tacrolimus involving 44 patients have indicated improvement in 87% and failure of response in 13%.35,38,50,276 The calcineurin inhibitors have been associated with serious side effects, including a paradoxical heightened state of autoreactivity, and endorsement of these agents as rescue therapies has not been universal.49,277 Furthermore, the calcineurin inhibitors have mainly immunosuppressive rather than anti-inflammatory effects, and they have not been effective in preventing autoimmune hepatitis after liver transplantation.113,278
Treatment with the calcineurin inhibitors is commonly indefinite, and it requires experience to ensure careful monitoring and appropriate dose adjustment. Cyclosporine (Neoral) has been administered in doses of 2 to 5 mg/kg body weight with dose adjustments to achieve trough levels of 100 to 300 ng/mL,34,36,49 and tacrolimus has been administered at a starting dose of 0.5 to 1 mg daily and increased to 1 to 3 mg twice daily as tolerated to achieve a serum level of 3 ng/mL (range, 1.7 to 10.7 ng/mL).34,35,38,49,276,279
Small clinical experiences with rapamycin (sirolimus), rituximab, and infliximab have illustrated the continuing effort that is being expended to develop rescue therapies that can supplant or supplement current corticosteroid-based regimens for auto-immune hepatitis.34,49,54,253 Rapamycin (1 to 3 mg daily adjusted to maintain blood levels of 5 to 8 μg/dL) has suppressed the inflammatory manifestations of six patients with recurrent or
Rituximab has improved isolated cases of autoimmune hepatitis with idiopathic thrombocytopenic purpura,281 cryoglobulinemic glomerulonephritis,282 previous B cell lymphoma,283 and Evans syndrome (hemolytic anemia and idiopathic thrombocytopenia),284 and rituximab (two infusions of 1,000 mg 2 weeks apart) has reduced serum AST levels in all six treated patients, improved histological features in four biopsied patients, and allowed corticosteroid withdrawal in three of four patients in a small treatment trial (Table 8).285
Similarly, a small trial of infliximab (infusions of 5 mg/kg body weight at time zero, 2 weeks, 6 weeks, and every 4 to 8 weeks thereafter) in 11 patients with refractory autoimmune hepatitis has normalized liver tests in eight patients, improved histological activity indices in five patients, and allowed treatment withdrawal in three patients (Table 8).55 The development of side effects (mainly infectious complications) in seven of the 11 patients receiving infliximab, including three patients (27%) who required discontinuation of the drug, underscores the importance of establishing safety profiles, dosing guidelines, and monitoring strategies for each drug under trial before considering routine clinical application.286–291
Liver transplantation is the ultimate rescue therapy for patients that present with features of liver failure or who develop these features during standard treatment.256 The 5- and 10-year patient survivals after liver transplantation exceed 70% in adults,118,292–294 and the 5-year survival is as high as 86% in children.295 Recurrent disease can progress to cirrhosis,296 and 13% to 50% of adults with recurrent disease develop graft failure.115,297,298 Retransplantation may be necessary with the understanding that autoimmune hepatitis may still recur.115,296 Importantly, serious consequences of recurrent autoimmune hepatitis have not been uniformly experienced in all centers. The actuarial 5-year survivals for patients and grafts after recurrent autoimmune hepatitis have been 100% and 87% in one experience,115 and patient and graft survivals have been similar to those of patients transplanted for nonautoimmune liver diseases in other experiences.118,297,299 The risk of recurrent auto-immune hepatitis after liver transplantation should not affect the transplant decision. Liver transplantation is indicated by a model of end-stage liver disease (MELD) score >16 points, acute decompensation, intractable symptoms, treatment intolerance, or detection of liver cancer.293
Most new therapeutic interventions have not moved beyond the theoretical stage in autoimmune hepatitis, but their premise and promise are founded on studies already performed in cell cultures, animal models, or preliminary clinical trials in other immune-mediated diseases.34,52,53,300,301 They await rigorous study in autoimmune hepatitis.
Monoclonal antibodies to tumor necrosis factor-α (infliximab)55 and monoclonal antibodies to CD20 (rituximab)285 have already begun an evaluation process in the treatment of autoimmune hepatitis (Table 8). Other molecular interventions that have advanced in animal studies and clinical trials outside autoimmune hepatitis also warrant consideration in this disease. Molecular interventions are intended to blunt or correct detrimental pathological mechanisms, but they may also interfere with normal homeostatic mechanisms and have unintended consequences. Their introduction as therapeutic agents requires an awareness of these possible consequences and rigorous evaluation in clinical trials.
Cytotoxic T lymphocyte antigen-4 fused with immunoglobulin (CTLA-4Ig) is a dimeric recombinant human fusion protein that is a homologue of the CD28 molecule expressed on the surface of CD4+ T lymphocytes (Table 8).52 CTLA-4Ig can interfere with the binding of CD28 with the B7 ligands (CD80 and CD86) expressed on antigen-presenting cells and prevent completion of the signaling pathway necessary for lymphocyte activation.302 CTLA-4Ig is already approved for use in rheumatoid arthritis, and it has improved the serological and histological manifestations of PBC in a murine model.303
Nonmitogenic monoclonal antibodies to CD3 target the T cell antigen receptor of T lymphocytes, and they can promote the apoptosis of immune cells (Table 8).300,304 The newly released apoptotic bodies can then be ingested by macrophages and dendritic cells, and these cells can in turn produce transforming growth factor β (TGF-β).305 Regulatory T cells that express the latency-associated peptide can be induced by TGF-β and expand the immunosuppressive effect.306 Antibodies to CD3 have already been shown to induce complete and durable remission in nonobese diabetic mice,307 and clinical trials have demonstrated its effectiveness in maintaining or increasing insulin production in patients with insulin-dependent autoimmune diabetes.308
Simtuzumab (GS-6624) is a monoclonal antibody that is directed against the enzyme that promotes the cross-linkage of collagen fibrils and expansion of extracellular matrix (Table 8). Simtuzumab has been safe and well-tolerated in Phase 1 studies involving patients with hepatic fibrosis, and this monoclonal antibody to lysyl oxidase-like 2 has entered Phase 2 clinical studies designed to prevent hepatic fibrosis in NAFLD and PSC (
Regulatory T cells and natural killer T cells are cell populations that help modulate immune reactivity, and they have been manipulated to suppress inflammatory and immune responses in animal models of diverse immune-mediated diseases (Table 8).59,300 Regulatory T cells can be expanded by pharmacological agents (corticosteroids, rapamycin, mycophenolate mofetil, and 1, 25 dihydroxyvitamin D3)59 or by the adoptive transfer of autologous cells that have been expanded or newly generated
Natural killer T cells have stimulatory and inhibitory actions on the innate and adaptive immune responses, and they are amenable to manipulation by antigenic stimuli that promote the desired predominant action (Table 8).59,300,314 Natural killer T cells expressing a semi-invariant antigen receptor recognize glycolipid antigens bound to the CD1 antigen-presenting molecule, and glycolipid antigens can be designed to elicit the preferred action of these cells.315 Natural killer T cells have been evaluated in animal models of type 1 diabetes, systemic lupus erythematosus, rheumatoid arthritis, and autoimmune encephalomyelitis,300 and studies in experimental autoimmune hepatitis have supported the further investigation of their pathogenic role and therapeutic implications in this disease.316,317
Mesenchymal stromal cells also affect the innate and adaptive immune responses by modulating the activity of macrophages, natural killer cells, and dendritic cells and by inhibiting the activity of B and T lymphocytes (Table 8).60 The adoptive transfer of mesenchymal stromal cells has been effective in murine models of rheumatoid arthritis and radiation-induced liver injury,301,318 and its therapeutic promise has been supported by preliminary human experiences in refractory Crohn’s disease, corticosteroid-resistant graft-versus-host disease, and allograft rejection after kidney transplantation.319–321 Serious side effects have not been encountered in mid-term human studies, but questions remain regarding the preferred expansion technique, the rare occurrence of immunogenicity in animal models, and the possible induction of chromosome aberrations, transient aneuploidy, or malignant transformations in cell cultures from murine and human sources.60 There have been no reported experiences in autoimmune hepatitis.320
The generation of reactive oxygen species from Kupffer cells and myofibroblasts promotes the apoptosis of hepatocytes, the release of apoptotic bodies, and the activation of hepatic stellate cells.322,323 Antioxidants (N-acetylcysteine, S-adenosyl-L-methionine, and vitamin E) have already been shown in clinical experiences to decrease histological activity, TGF-β production, and fibrosis in NAFLD (Table 8).324,325 They have also improved mortality in alcoholic cirrhosis,326 and enhanced early viral responses in chronic hepatitis C.327 Angiotensin inhibitors may inhibit the transformation of hepatic stellate cells into myofibroblasts, and losartan has decreased fibrosis in chronic hepatitis C.328 The antioxidants and the angiotensin inhibitors are feasible antiapoptotic and antifibrotic agents that warrant evaluation as adjunctive therapies in autoimmune hepatitis.329–332
Agents that reduce apoptosis are feasible interventions in autoimmune hepatitis if their actions can be directed to the pertinent cell population. Caspase inhibitors have reduced apoptosis in murine models of acute liver injury,333 bile duct ligation,334 NAFLD,335 and acute liver failure after massive hepatectomy.336 They have also been used in limited clinical experiences involving patients with chronic hepatitis C337,338 and NAFLD337 and in organs for liver transplantation to protect against ischemia/re-perfusion injury.339 The major concern is the possibility of unintended interference with normal apoptotic pathways that guard against the invasion of pathogens and the malignant transformation of cells.57 Caspase inhibitors have not been evaluated in autoimmune hepatitis.
Patients with chronic liver disease, including autoimmune hepatitis, have reduced serum levels of 25-hydroxyvitamin D, and this deficiency has been associated with disease severity and hepatic fibrosis.340–345 Vitamin D protects against oxidative stress, limits the proliferation of myofibroblasts, stimulates the expansion of regulatory T cells, reduces the production of pro-inflammatory cytokines, and modulates activation of immune effector cells.346–348 Low serum levels of 25-hydroxyvitamin D may compromise these diverse beneficial actions, and vitamin D supplementation may be a measure to bolster actions that protect hepatocytes.349 The impact of supplemental vitamin D therapy on the severity and responsiveness of corticosteroid-treated autoimmune hepatitis also requires evaluation.
Table 1 Nonclassical Phenotypes of Autoimmune Hepatitis at Presentation
| Nonclassical phenotype | Features | Implications |
|---|---|---|
| Acute onset | Frequency, 25%–75%63,65 | Can resemble acute viral, drug-induced, toxic or ischemic injury61 |
| Acute severe (fulminant) onset | Frequency, 3%–6%66,67 | Can resemble acute viral, drug-induced, toxic or ischemic injury61 |
| Asymptomatic presentation | Frequency, 25%–34%72,73 | Low frequency of resolution if untreated (12% vs 63%)74 |
| Autoantibody-negative phenotype | Scoring systems diagnostic, 19%–22%75 | Steroid-responsive, 67%–87%75,81 |
| Atypical histological patterns | Centrilobular necrosis in 29%94 | May reflect severity and acuity of AIH94 or suggest other diagnoses102 |
| Graft dysfunction posttransplant | Recurrent AIH, 8%–12% after 1st year122 | Variable steroid response113 |
| Overlap syndrome | Mixed features of AIH+PBC or PSC102,107 | Variable treatment response52,53 |
CT, computed tomography; AIH, autoimmune hepatitis; anti-SLA, antibodies to soluble liver antigen; anti-GSTT1, antibodies to glutathione-S-transferase T1; PBC, primary biliary cholangitis; PSC, primary sclerosing cholangitis; UDCA, ursodeoxycholic acid.
Table 2 Comprehensive Diagnostic Scoring System of the International Autoimmune Hepatitis Group
| Clinical features | Points | Clinical features | Points |
|---|---|---|---|
| Female | +2 | Average alcohol intake (g/day) | |
| <25 | +2 | ||
| >60 | −2 | ||
| AP:AST (or ALT) ratio | Histologic findings | ||
| <1.5 | +2 | Interface hepatitis | +3 |
| 1.5–3.0 | 0 | Lymphoplasmacytic infiltrate | +1 |
| >3.0 | −2 | Rosette formation | +1 |
| Biliary changes | −3 | ||
| Other atypical changes | −3 | ||
| None of above | −5 | ||
| Serum globulin or IgG level above ULN | Concurrent immune disease, including celiac disease | +2 | |
| >2.0 | +3 | Other autoantibodies | +2 |
| 1.5–2.0 | +2 | HLA DRB1*03 or DRB1*04 | +1 |
| 1.0–1.5 | +1 | ||
| <1.0 | 0 | ||
| ANA, SMA, or anti-LKM1 | Response to corticosteroids | ||
| >1:80 | +3 | Complete | +2 |
| 1:80 | +2 | Relapse after drug withdrawal | +3 |
| 1:40 | +1 | ||
| <1:40 | 0 | ||
| AMA positive | −4 | ||
| Hepatitis markers | Aggregate score pretreatment | ||
| Positive | −3 | Definite autoimmune hepatitis | >15 |
| Negative | +3 | Probable autoimmune hepatitis | 10–15 |
| Hepatotoxic drug exposure | Aggregate score posttreatment | ||
| Positive | −4 | Definite autoimmune hepatitis | >17 |
| Negative | +1 | Probable autoimmune hepatitis | 12–17 |
AP, alkaline phosphatase; AST, aspartate aminotransferase; ALT, alanine aminotransferase; IgG, immunoglobulin G; ULN, upper limit of the normal range; HLA, human leukocyte antigen; ANA, antinuclear antibodies; SMA, smooth muscle antibodies; anti-LKM1, antibodies to liver kidney microsome type 1; AMA, antimitochondrial antibodies.
Adapted from Alvarez F,
Table 3 Simplified Diagnostic Scoring System of the International Autoimmune Hepatitis Group
| Category | Scoring elements | Results | Points |
|---|---|---|---|
| Autoantibodies | ANA or SMA | 1:40 by IIF | +1 |
| ANA or SMA | ≥1:80 by IIF | +2 | |
| Anti-LKM1 (alternative to ANA and SMA) | ≥1:40 by IIF | +2 | |
| Anti-SLA (alternative to ANA, SMA and LKM1) | Positive | +2 | |
| Immunoglobulins | Immunoglobulin G level | >ULN | +1 |
| >1.1 times ULN | +2 | ||
| Histological findings | Interface hepatitis | Compatible features | +1 |
| Typical features | +2 | ||
| Viral markers | IgM anti-HAV, HBsAg, HBV DNA, HCV RNA | No viral markers | +2 |
| Probable diagnosis | ≥6 | ||
| Definite diagnosis | ≥7 |
ANA, antinuclear antibodies; SMA, smooth muscle antibodies; anti-LKM1, antibodies to liver kidney microsome type 1; SLA, soluble liver antigen; IIF, indirect immunofluorescence; ULN, upper limit of the normal range; IgM, immunoglobulin M; HAV, hepatitis A virus; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; DNA, deoxyribonucleic acid; HCV, hepatitis C virus; RNA, ribonucleic acid.
Adapted from Hennes EM,
Table 4 Standard Antibodies for the Diagnosis of Autoimmune Hepatitis
| Standard antibodies | Antigenic target(s) | Clinical features |
|---|---|---|
| ANA | Centromere, ribonucleoproteins, ribonucleoprotein complexes, histones160,161 | Lacks organ and disease specificity156 |
| Present in 80% of adults with AIH156 | ||
| Occurs in 20%–40% with non-AIH156–158 | ||
| Sensitivity for AIH when isolated finding, 32%156 | ||
| Specificity for AIH when isolated finding, 76%156 | ||
| Diagnostic accuracy for AIH, 56%156 | ||
| Concurrent ANA and SMA most diagnostic (74%)156 | ||
| Titers can vary outside disease activity86,156 | ||
| SMA | Filamentous (F) actin, 86%162 | Lacks organ and disease specificity156 |
| Nonactin components, 14%162 | Present in 63% of adults with AIH156 | |
| Occurs in 3%–16% with non-AIH156–158 | ||
| Sensitivity for AIH when isolated finding, 16%156 | ||
| Specificity for AIH when isolated finding, 96%156 | ||
| Diagnostic accuracy for AIH, 61%156 | ||
| Concurrent SMA and ANA most diagnostic (74%)156 | ||
| Titers >1:80 associated with disease activity159 | ||
| Anti-LKM1 | Cytochrome P450 2D6167,168 | Present in 3% of North American adults with AIH149 |
| Detected in 14%–38% of British children with AIH11,163 | ||
| Occurs in 0%–10% of chronic hepatitis C156,164–166 | ||
| Low concurrence with SMA and ANA, 2%156 | ||
| High specificity (99%), low sensitivity (1%)156 | ||
| Diagnostic accuracy in North American adults, 57%156 |
ANA, antinuclear antibodies; AIH, autoimmune hepatitis; SMA, smooth muscle antibodies; anti-LKM1, antibodies to liver kidney microsome type 1.
Table 5 Nonstandard Antibodies for the Diagnosis of Autoimmune Hepatitis
| Nonstandard antibodies | Antigenic target(s) | Clinical features |
|---|---|---|
| Antibodies to actin (antiactin) | Filamentous (F) actin162 | Present in 87% with AIH162,170,172 |
| Nonactin components162 | Concurrent with SMA in 86%–100% with AIH162,173 | |
| SMA without antiactin in 14% with AIH162 | ||
| Indirect marker of disease activity159,162 | ||
| No standardized assay162,177 | ||
| Antibodies to α-actinin (anti-α-actinin) | α-Actinin178 | Present in 42% of patients with AIH27 |
| Antiactin+anti-α-actinin associated with severity27 | ||
| Baseline level predictive of treatment response30 | ||
| Investigational assay not generally available27,30 | ||
| Antibodies to soluble liver antigen (anti-SLA) | Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase (SEPSECS)23,182,183 | Present in 7%–22% with AIH26,31,87,179,180 |
| Genetic association with HLA DRB1*030124,25 | ||
| Associated with severity, response, relapse, survival24–26 | ||
| Useful in diagnosing seronegative patients159,180,181 | ||
| Specificity, 99%, and sensitivity, 11%179 | ||
| Atypical perinuclear antineutrophil cytoplasmic antibodies (pANCA) | β-Tubulin isotype 5189 | Cross reacts with precursor bacterial protein (FtsZ)189 |
| Present in 50%–92% with typical AIH88,187–189 | ||
| Absent in anti-LKM1-positive AIH190 | ||
| Detected in CUC, PSC, PBC, minocycline injury188,191,193 | ||
| Useful in classifying seronegative AIH17,76,171,195 | ||
| Antibodies to asialoglycoprotein receptor (anti-ASGPR) | Asialoglycoprotein receptor198,199 | Present in 67%–88% with AIH28,198–201 |
| Occurs in other acute and chronic liver diseases198,203,204 | ||
| Useful in classifying seronegative AIH205 | ||
| Correlates with laboratory and histological activity206 | ||
| May predict relapse and define treatment end points201,206 | ||
| Antibodies to liver cytosol type 1 (anti-LC1) | Formiminotransferase cyclodeaminase219–222 | Present in 24%–32% of anti-LKM1-positive AIH208–210 |
| Occurs in chronic hepatitis C and anti-LKM1211–214 | ||
| Useful in classifying seronegative AIH217,218 | ||
| Rare in North American adults with AIH216 |
AIH, autoimmune hepatitis; SMA, smooth muscle antibodies; HLA, human leukocyte antigen; anti-LKM1, antibodies to liver kidney microsome type 1; CUC, chronic ulcerative colitis; PSC, primary sclerosing cholangitis; PBC, primary biliary cholangitis.
Table 6 Standard Drug Regimens for Autoimmune Hepatitis
| Clinical situation | Combination therapy | Monotherapy | |
|---|---|---|---|
| Prednisone or prednisolone | Azathioprine | Prednisone or prednisolone | |
| xTreatment-naïve* | 30 mg daily×1 wk17,18,34 | 50 mg daily fixed dose17,18,34 | 60 mg daily×1 wk17,18,34 |
| 20 mg daily×1 wk | 40 mg daily×1 wk | ||
| 15 mg daily×2 wk | 30 mg daily×2 wk | ||
| 10 mg daily maintenance | 20 mg daily maintenance | ||
| Treatment failure | 30 mg daily×1 mo253,256 | 150 mg daily×1 mo253,256 | 60 mg daily×1 mo253,256 |
| 20 mg daily×1 mo if improved | 100 mg daily×1 mo if improved | Reduce dose by 10 mg for each month of improvement until 20 mg daily maintenance | |
| 10 daily maintenance if improvement continues | 50 mg daily maintenance if improvement continues | ||
| Increase dose to last level of improvement×1 mo if worsens | Increase dose to last level of improvement×1 mo if worsens | Increase dose to last level of improvement×1 mo if worsens | |
| Increase to 30 mg daily if worsening continues | Increase to 150 mg daily if worsening continues | Increase to 60 mg daily if worsening continues | |
| Incomplete response | 10 mg daily253 | 2 mg/kg daily253 | 20 mg daily253 |
| Dose reductions to maintain normal or near-normal liver tests with goal of drug withdrawal | Fixed dose as steroid dose reduced or discontinued with goal of indefinite azathioprine maintenance | Dose reductions to lowest dose possible to maintain normal or near-normal liver tests | |
| Drug intolerance | Decrease dose or discontinue steroid17,253 | Decrease dose or discontinue azathioprine17,253 | Decrease dose or discontinue steroid17,253 |
| Increase azathioprine dose to 100 or 150 mg daily if necessary | Increase dose of steroid as needed or cautiously consider mycophenolate mofetil, 1–2 g daily41,45,46 | Add azathioprine, 50 mg daily, and adjust dose | |
| Relapse after drug withdrawal | Resume original regimen until resolution of liver tests | Resume original regimen until resolution of liver tests | Resume original regimen for until resolution of liver tests |
| Gradually withdraw and discontinue as dose of azathioprine increased17,253 | Increase dose to 2 mg/kg daily and continue indefinitely17,32,253 | Decrease steroid dose to lowest level and maintain indefinitely17,253,259 | |
*Treatment-naïve regimens in Europe commonly include prednisolone at 1 mg/kg daily and azathioprine at 1–2 mg/kg daily.33,234,235
Table 7 Alternative Drug Regimens for Autoimmune Hepatitis
| Clinical situation | Budesonide | Mycophenolate mofetil | Calcineurin inhibitors |
|---|---|---|---|
| Treatment-naïve | 6–9 mg daily combined with azathioprine, 1–2 mg daily44 | 1.5–2 g daily combined with prednisolone, 0.5–1 mg/kg daily47 | Cyclosporine, 2–5 mg/kg daily (trough, 100–300 ng/mL)36 |
| Outcomes in juvenile AIH equivalent to standard therapy266 | No established superiority over standard therapy34 | Tacrolimus, 3 mg twice daily (serum level, 3 ng/mL)35 | |
| Preferred in mild, noncirrhotic, uncomplicated AIH and patients with low steroid tolerance34 | Equivalent to standard combination therapy and not preferred51,274,275 | ||
| Treatment failure | Not effective in limited trial271 | Effective in 23%34,50 | Cyclosporine effective in 93%49 |
| Side effects with cirrhosis268,269 | Avoid in pregnancy and severe cytopenia49,272,273 | Tacrolimus effective in 87%38,276 | |
| Low enthusiasm despite success49,277 | |||
| Drug intolerance | Difficult to switch with prednisone without severe withdrawal symptoms271 | Effective in 58%34,50 | Limited use in steroid intolerance and associated with other complexities36,49 |
| Avoid in pregnancy and severe cytopenia49,272,273 |
AIH, autoimmune hepatitis.
Table 8 Emerging Molecular, Cellular and Pharmacological Interventions for Autoimmune Hepatitis
| Emerging interventions | Putative actions | Experience |
|---|---|---|
| Molecular interventions | ||
| CTLA-4Ig (abatacept) | Disrupts CD28 binding to B7 ligands52 | Approved for rheumatoid arthritis52 |
| Dampens T lymphocyte activation34,300 | Improved murine model of PBC303 | |
| Anti-CD20 (rituximab) | Inhibits B lymphocyte activation53,300 | Isolated patients with AIH281–284 |
| Effective in refractory AIH285 | ||
| Anti-TNF-α (infliximab) | Inhibits TNF-α and interferes with maturation of cytotoxic T cells34,52 | Effective in refractory AIH55 |
| Frequent side effects (27%)55 | ||
| Nonmitogenic anti-CD3 | Binds to antigen receptor of T cells300 | Effective in diabetic model307 |
| Promotes apoptosis of immune cells34,53 | Increases insulin in diabetic humans308 | |
| Anti-lysyl oxidase-like 2 (simtuzumab) | Inhibits lysyl oxidase and antifibrotic323 | Phase 2 studies to prevent fibrosis in NAFLD and PSC (https://clinicaltrials.gov) |
| Prevents cross-linkage of collagen322 | ||
| Cellular interventions | ||
| Adoptive transfer of regulatory T cells | Corrects deficiencies in cell population60 | Effective in models of AIH56,312 |
| Expands immune regulatory population60 | Effective in model of PBC313 | |
| Adoptive transfer of mesenchymal stromal cells | Affects innate and adaptive immunity60 | Effective in models of RA301 |
| Inhibits B and T lymphocytes60 | Promising in early human studies319–321 | |
| Modulation of natural killer T cells | Tailored glycolipid antigens skew dual immune actions favorably59,314,315 | Effective in animal models of diabetes, RA, SLE and AIH300,316,317 |
| Pharmacological prospects | ||
| Antioxidants (N-acetylcysteine, S-adenosyl-L methionine) | Reduce reactive oxygen species322,323 | Effective in NAFLD, chronic hepatitis C, and alcoholic cirrhosis324–327 |
| Decrease hepatocyte apoptosis322,323 | ||
| Inhibit stellate cell activation322,323 | ||
| Angiotensin inhibitors (losartan) | Reduce profibrotic transformation of hepatic stellate cells to myofibroblasts322 | Decreased fibrosis in chronic hepatitis C328 |
CTLA-4Ig, cytotoxic T lymphocyte antigen-4 fused with human immunoglobulin; PBC, primary biliary cholangitis; AIH, autoimmune hepatitis; TNF-α, tumor necrosis factor-alpha; NAFLD, nonalcoholic fatty liver disease; PSC, primary sclerosing cholangitis; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus.
pISSN 1976-2283
eISSN 2005-1212
Gut and Liver is an international journal of gastroenterology, focusing on the gastrointestinal tract, liver, biliary tree, pancreas, motility, and neurogastroenterology. Gut atnd Liver delivers up-to-date, authoritative papers on both clinical and research-based topics in gastroenterology. The Journal publishes original articles, case reports, brief communications, letters to the editor and invited review articles in the field of gastroenterology. The Journal is operated by internationally renowned editorial boards and designed to provide a global opportunity to promote academic developments in the field of gastroenterology and hepatology. +MORE
| Yong Chan Lee |
Professor of Medicine Director, Gastrointestinal Research Laboratory Veterans Affairs Medical Center, Univ. California San Francisco San Francisco, USA |
| Jong Pil Im | Seoul National University College of Medicine, Seoul, Korea |
| Robert S. Bresalier | University of Texas M. D. Anderson Cancer Center, Houston, USA |
| Steven H. Itzkowitz | Mount Sinai Medical Center, NY, USA |
All papers submitted to Gut and Liver are reviewed by the editorial team before being sent out for an external peer review to rule out papers that have low priority, insufficient originality, scientific flaws, or the absence of a message of importance to the readers of the Journal. A decision about these papers will usually be made within two or three weeks.
The remaining articles are usually sent to two reviewers. It would be very helpful if you could suggest a selection of reviewers and include their contact details. We may not always use the reviewers you recommend, but suggesting reviewers will make our reviewer database much richer; in the end, everyone will benefit. We reserve the right to return manuscripts in which no reviewers are suggested.
The final responsibility for the decision to accept or reject lies with the editors. In many cases, papers may be rejected despite favorable reviews because of editorial policy or a lack of space. The editor retains the right to determine publication priorities, the style of the paper, and to request, if necessary, that the material submitted be shortened for publication.
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