eISSN: 1644-4124
ISSN: 1426-3912
Central European Journal of Immunology
Current issue Archive Manuscripts accepted About the journal Abstracting and indexing Subscription Contact Instructions for authors
SCImago Journal & Country Rank

vol. 35

Clinical immunology
Laboratory diagnosis of autoimmune hepatitis

Urszula Demkow

Centr Eur J Immunol 2010; 35 (1): 37-40
Online publish date: 2010/04/06
Article file
- Laboratory diagnosis.pdf  [0.06 MB]
Get citation
JabRef, Mendeley
Papers, Reference Manager, RefWorks, Zotero
Autoimmune liver diseases include 3 distinct disease entities: autoimmune hepatitis (AIH), primary biliary cirrhosis (PBC) and primary sclerosing cholangitis (PSC) [1]. In most cases each condition is associated with distinct serological profile, morphological changes, clinical course and response to therapy although overlapping syndromes also have been described [2]. Autoimmune hepatitis is a disease characterised by inflammation and destruction of the hepa­tic parenchyma which shows a good response to immunosuppressive therapy. PBC and PSC are primarily autoimmune diseases of the biliary tract [3, 4]. In PBC, damage is restricted to the small intralobular bile ducts whereas, in PSC the extrahepatic and/or intrahepatic ducts may be affected. Autoimmune etiology of these diseases is proved by the presence of hypergammaglobulinemia and of a variety of autoantibodies. Additionally, up to 70% of patients with these conditions have at least one concomitant immunological disorder, most frequently Sjögren’s syndrome, rheumatoid arthritis, thyroiditis, diabetes or ulcerative colitis [1]. Although familial AIH, PBC, or PSC is rare, there appears to be an underlying genetic susceptibility to each condition as evidenced by well established associations with various HLA haplotypes or allotypes, several of which are also associated with other autoimmune disorders [1, 5].
There is no specific diagnostic test for autoimmune hepatic diseases. Diagnosis is based on careful exclusion of other causes of chronic liver disease like viral, metabolic, genetic and toxic aetiologies of chronic hepatitis or hepatic injury, together with the finding of several suggestive laboratory markers like autoantibodies, some of which, such as antimitochondrial antibodies (AMA) in PBC, are relatively disease-specific but most others, such as anti-nuclear antibodies, are non-specific markers. The diseases can be confirmed by histological examination revealing specific morphological changes [1, 4].
Autoantibodies contribute to the diagnosis of AIH and have led to the serological subclassification into three distinct types [1, 4]. Based on these results, a serological subclassification of AIH has been developed [6-8]. Although this classification remains controversial, it has resulted in the delineation of three subtypes which can be distinguished on the basis of the presence of different autoantibodies (Figure 1). The classical form of AIH (type 1) displays antinuclear antibodies (ANA.) This form of AIH represents 80% of all cases of AIH, making it the most prevalent subclass. Antinuclear antibodies show specificity for both functional and structural proteins in the cell nucleus. They can be directed against nuclear membranes, proteins or DNA [8-13]. Unfortunately the target antigens are heterogeneous and incompletely defined even within a single disease such as AIH. For the diagnostic work-up of AIH the molecular characterization of target antigen specificity does not supply important additional information to increase diagnostic precision [8]. Screening determinations of ANA are routinely performed by indirect immunofluorescence on cryostat sections of rat liver and on Hep 2 cell slides [8]. Most commonly, a homogeneous or speckled immunofluorescence pattern is demonstrable. Antinuclear antibodies have been found to be reactive with an array of antigens. They represent the most common autoantibody in AIH and occur in high titres usually exceeding 1 : 160. However, the titre does not correlate with the course of disease, prognosis, progression, requirement of transplantation or disease activity [8]. Anti-smooth muscle antibodies (SMA) are directed against cytoskeletal proteins such as actin, troponin and tropomyosin [14, 15]. They frequently occur in high titres in association with ANA. They are not highly specific for AIH and have been shown to occur in advanced liver diseases of other etiologies, in infectious diseases and in rheumatic disorders. In these cases titres are often lower than 1 : 80. SMA autoantibodies are also determined by indirect immunofluorescence on cryostat sections of rat stomach. In paediatric patients, SMA autoantibodies may be the only marker of AIH type 1. When present in very young patients with AIH type 1 the titres may be as low as 1 : 40. The patients with type 2 of AIH have autoantibodies directed against antigens expressed in the endoplasmic reticulum (ER) termed anti-microsomal autoantibodies, these were shown to possess specificity against cytochrome P450 monoxygenases expressed in the ER. Anti-microsomal antibodies are directed against CYP2D6 – expressed not only in the liver but also in the kidney (liver/kidney microsomal antibodies LKM) [8, 16-18]. The third serological group of AIH (type 3) present with an antibody directed against a protein present in the 100 000 γ supernatant of liver homogenate [8, 17]. This was termed anti-soluble liver antigen; it was independently described as anti-liver pancreas autoantibody (SLA/LP) [6, 18-20]. SLA/LP autoantibo­dies have recently been shown to be directed against a UGA repressor t-RNA-associated protein [21-24]. These two antibodies have been reported in only about 30% of patients, and some of these patients do not have ANA, SMA, or anti-LKM1. There is some evidence that anti-SLA and anti-LP are one and the same autoantibody. These findings represent a major advance in the study of autoimmune hepatitis [25]. Investigators claim that anti-SLA/LP has 100% specificity (with 30% sensitivity) for autoimmune hepatitis. Cloning of SLA/LP provided the opportunity for the development of a simple and widely available test for the antibody. Type 3 shares clinical similarity with AIH type 1; because of this similarity, it is believed by some researchers not to represent a distinct subclass of its own [4, 26]. 70-80% of patients with AIH present with high titres ANA, SMA, SLA/LP or anti-LKM, but diagnosis can be difficult in the 20–30% who do not have these markers [6, 25]. Many such patients have other autoantibodies, including those showing perinuclear staining on neutrophils (pANCA) and antibodies reacting with the hepatocyte-specific asialoglycoprotein receptor (ASGPR) [6, 25]. However, testing for anti-ASGPR is not yet widely available and neither this antibody nor pANCA is exclusive to autoimmune hepatitis. single underlying mechanism but is most likely a group of diseases with a similar clinical presentation. In view of his, it is interesting to note that AIH occurs in 10% of patients with autoimmune polyglandular syndrome type 1 (APS-1) [6, 26]. Autoimmune polyglandular syndrome type 1 combines hypoparathyroidism, mucocutaneous fungal infections, adrenal insufficiency and a number of other immune-mediated symptoms such as nail dystrophy, vitiligo and alopecia. In patients with APS-1 who develop AIH, autoantibodies are present which are also directed against CYP proteins, namely, CYP1A2 and CYP2A6 [6, 27].
Primary sclerosing cholangitis (PSC) is a chronic and progressive cholestatic liver disease, which is characterized by inflammation and fibrosis of mainly the large bile ducts leading to biliary cirrhosis in a high percentage of patients [28, 29]. Primary sclerosis cholangitis usually involves both the intrahepatic and extrahepatic biliary tree. It is often associated with underlying inflammatory bowel disease, especially ulcerative colitis [28]. After secondary causes of sclerosing cholangitis are eliminated, biochemical tests, clinical presentation, and histology suggest the diagnosis [28, 29]. In PSC multiple non-specific autoantibodies, which are rather epiphenomena to chronic inflammation, can be found including ANA in 7-77%, anticardiolipin antibodies in 4–66%, SMA antibodies in 13-20%, anti-thyroid peroxidase (TPO) antibodies in 16% and rheumatoid factor in 15% [28, 29]. Atypical perinuclear-staining, antineutrophil antibodies (p-ANCA) can be found in 60-93% of patients with PSC but also in patients with AIH. Anti-neutrophil antibodies associated with PSC are distinct from c-ANCA and classical p-ANCA which are commonly used as diagnostic and therapeutic seromarkers for Wegeners granulomatosis and microscopic polyangiitis, respectively. Primary sclerosis cholangitis, ulcerative colitis and autoimmune he­pa­titis are associated with atypical p-ANCA which has a distinct staining pattern on indirect immunofluorescence microscopy [30]. Although a few studies have demonstrated some correlation between particular clinical parameters and the presence of autoantibodies, there is presently insufficient evidence to make use of any of them in determining prognosis. Most are present at low prevalence and at relatively low titres [28, 29].
Primary biliary cirrhosis (PBC) is a chronic liver disease characterised by cholestasis, antimitochondrial antibody (AMA) and lymphocyte-predominant portal inflammation with a variable degree of fibrosis. While its pathogenesis remains obscure, considerable progress has been made in characterizing the autoantibody response that occurs in PBC. Seropositivity for AMA antibody is not specific for the disease, but remains highly sensitive (98%) [31]. The targets of the AMA response are enzymatic members of the family of the 2-oxo-acid dehydrogenase complexes [31, 32]. Approximately 90–95% of PBC serum samples react against the pyruvate dehydrogenase E2 complex. Antimitochondrial antibody are very heterogeneous with respect to antigen specificity and polyclonality of the B-cell response leading to their formation [32]. These factors, combined with antibody avidity and expression of immunoglobulin isotypes and subclasses, can account for considerably variable inter-laboratory sensitivity and specificity in the detection of AMA. Antimitochondrial antibody can be detected by IIF, complement fixation, immunodiffusion, radioimmunoassay (RIA), enzyme linked immunosorbent assay (ELISA), immunoblotting (IB), and a novel functional assay that depends on demonstrating inhibition of the catalytic activity of the respective enzyme [32]. For IIF, some laboratories employ commercially prepared HEp-2 substrates, although other laboratories use the conventional cryopreserved rodent kidney substrates [32]. A shortcoming of IIF techniques is that, compared to ELISA, they lack sensitivity and the ability to distinguish autoantibodies to specific molecular targets [32]. An advantage of IIF, especially when HEp-2 substrates are used, is the ability to detect other relevant autoantibodies such as those directed against nuclear pore complexes, centromere and other intracellular antigens that may have diagnostic and prognostic importance in PBC. In the near future, new test systems and assays are emerging and they include bead technology and other solid phase antigen arrays [32]. Each assay has limitations when determining the sensitivity, specificity and the positive predictive value for the detection of AMA. For most clinical cases, the detection of pyruvate dehydrogenase complex-E2 (PDC-E2) alone may be sufficient to ensure the diagnosis [5, 32]. However, to achieve acceptable diagnostic relevance (i.e., positive predictive value) more than one assay may be required [32]. The simultaneous detection of autoantibodies to numerous antigens in a single assay, such as the mocroarray technique, may provide useful alternatives to current protocols. Although AMA is considered the humoral hallmark of PBC, antibodies against various mitochondrial enzymes can be frequently detected in patients with infectious liver diseases [32]. Depending on the assay used, up to 15% of PBC patients have been found to be AMA-negative. Sera from a subgroup of patients, including some AMA-negative patients, are positive for antibodies to nuclear components including Sp100, promyelocytic leukemia proteins, and two components of the nuclear pore complex. Antinuclear antibodies are also detectable in approximately 50% of subjects with PBC. Two particular autoantibodies, those that recognize nuclear pore membrane protein gp210 and those against nuclear body protein sp100, appear to be highly specific and detectable in approximately 25% of individuals with PBC. ANA against other nuclear envelope and nuclear body proteins also occur less frequently but appear to be highly specific for PBC [33]. Most clinical laboratories use indirect immunofluorescence microscopy to detect ANA and two labeling patterns that predominate in PBC are punctate nuclear rim and multiple nuclear dots. Antibodies giving these patterns most often recognize nuclear pore membrane protein gp210 and nuclear body protein sp100, respectively. These ANA are highly specific for PBC and detected in approximately 25% of patients [33]. Less frequently, ANA apparently unique to PBC recognize other proteins of the nuclear envelope and nuclear bodies. The antibodies against gp210, sp100 and some other nuclear proteins are very specific to PBC and may therefore be useful diagnostic markers. The clinical significance of ANA in PBC has been widely investigated and data indicate that, unlike AMA, they are not associated with disease severity and may be present many years before other clinical, biochemical, or histological manifestations occur. Antinuclear antibody and smooth muscle antibody arise in 35% and 66% of patients with primary biliary cirrhosis, respectively [32, 33]. Serum anticentromere antibodies in patients affected by the CREST syndrome (calcinosis, Raynaud’s phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasias) are noted in 10-15% of instances. Other autoantibodies in association with the disease include rheumatoid factor (70%) and antithyroid (antimicrosomal, antithyroglobulin) antibodies (40%) [33].
Although much progress has been made in the understanding of the clinical expression of autoimmune hepatitis, its pathogenesis remains obscure despite more than 30 years of research [6]. There is considerable evidence pointing to a genetic susceptibility to the disease, [1, 5, 6] which may be related to one or more defects in the control of liver autoreactivity [25]. A characteristic feature of AIH is the fact that none of the major autoantigens detected by common autoantibodies in AIH are liver-specific, and not all are disease-specific. The diagnosis of AIH therefore rely on autoantibodies as a single positive identification marker. It is rather a diagnosis reached by the exclusion of other factors leading to chronic hepatitis, which include viral, toxic, genetic and metabolic aetiologies. The diagnosis of AIH is a probability best reflected in the AIH diagnostic score [4]. The most typical constellations of the antibodies for autoimmune liver diseases are presented in Table 1.

1. McFarlane IG, Heneghan MA (2004): Autoimmunity and the female liver. Hepatology Research 28: 171-176.  
2. Manns MP (1998): The concept of autoimmune liver diseases. In: Krawitt EL, Wiesner RH, Nishioka M, editors. Autoimmune liver diseases. 2nd ed. Amsterdam: Elsevier: 21-34.  
3. Dienes HP, Erberich H, Dries V, Schirmacher P, Lohse A (2002): Autoimmune hepatitis and overlap syndromes. Clin. Liver Dis.6: 349-362.  
4. International Autoimmune Hepatitis Group Report: review of criteria for diagnosis of autoimmune hepatitis. (1999): J Hepatol 31: 929-938.  
5. Strettell MDJ, Donaldson PT, Thomson LJ et al. (1997): Allelic basis for HLA-encoded susceptibility to type 1 autoimmune hepatitis, Gastroenterology 112: 2028-2035.
6. Strassburg CP, Manns MP (2003): Autoimmune hepatitis Best Practice & Research in Clinical Gastroenterology 17: 291-306.  
7. Manns MP, Strassburg CP (2001): Autoimmune hepatitis: clinical challenges, Gastroenterology 120: 1502-1517.  
8. Strassburg CP, Manns MP (1999): Antinuclear antibody (ANA) patterns in hepatic and extrahepatic autoimmune disease. Journal of Hepatology 31: 751-756.  
9. Strassburg C, Alex B, Zindy F et al. (1996): Identification of cyclin A as a molecular target of antinuclear antibodies (ANA) in hepatic and non-hepatic autoimmune diseases. J Hepatol 25: 859-866.
10. Tan MT (1991): Autoantibodies in pathology and cell biology. Cell 67: 841-842.
11. Czaja AJ, Nishioka M, Morhed SA, Haciya T (1994): Patterns of nuclear immunofluorescence and reactivities to recombinant nuclear antigens in autoimmune hepatitis. Gastroenterology 107: 200-207.
12. Czaja AJ, Ming C, Shirai M, Nishioka M (1995): Frequency and significance of antibodies to histones in autoimmune hepatitis. J Hepatol 23: 32-38.
13. Czaja AJ, Cassani F, Cataleta M et al. (1996): Frequency and significance of antibodies to actin in type 1 autoimmune hepatitis. Hepatology 24: 1068-1073.
14. Toh BH (1979): Smooth muscles autoantibodies and autoantigens. Clin Exp Immunol 1979; 38: 621-628.
15. Obermayer-Straub P, Strassburg CP, Manns MP (2000): Target proteins in human autoimmunity: cytochromes P450 and UDP- glucuronosyltransferases. Can J Gastroenterol. 2000; 14: 429-439.
16. Zanger UM, Hauri HP, Loeper J et al. (1988): Antibodies against human cytochrome P-450db1 in autoimmune hepatitis type 2. Proc Natl Acad Sci U S A 85: 8256-8260.
17. Guenguen M, Meunier-Rotival M, Bernard O, Alvarez F (1988): Anti-liver-kidney microsome antibody recognizes a cytochrome P450 from the IID subfamily. J Exp Med 168: 801-811.
18. Homberg JC, Abuaf N, Bernard O et al. (1987): Chronic active hepatitis associated with anti liver/kidney microsome type 1: a second type of “autoimmune” hepatitis. Hepatology 7: 1333-1339.
19. Manns M, Gerken G, Kyriatsoulis A et al. (1987): Characterization of a new subgroup of autoimmune chronic active hepatitis by autoantibodies against a soluble liver antygen. Lancet 1: 292-294.
20. Stechemesser E, Klein R, Berg PA (1993): Characterization and clinical relevance of liver-pancreas antibodies in autoimmune hepatitis. Hepatology 18: 1-9.
21. Costa M, Rodriguez-Sanchez JL, Czaja AJ, Gelpi C (2000): Isolation and characterization of cDNA encoding the antigenic protein of the human tRNP(Ser)Sec complex recognized by autoantibodies from patients with type-1 autoimmune hepatitis. Clin Exp Immunol 12: 364-374.
22. Gelpi C, Sontheimer E, Rodriguez-Sanchez J (1992): Autoantibodies against a serine tRNA-protein complex implicated in cotranslational selenocysteine insertion. Proc Nat Acad Sci U S A 89: 9739-9743.
23. Wies I, Brunner S, Henninger J et al. (2000): Identification of target antigen for SLA/LP autoantibodies in autoimmune hepatitis. Lancet 355: 1510-1515.
24. Volkmann M, Martin L, Bäurle A et al. (2001): Soluble liver antigen: isolation of a 35 kD recombinant protein (SLA-P35) specifically recognizing sera from patients with autoimmune hepatitis type 3. Hepatology 33: 591-596.
25. McFarlane IG (2000): Lessons about antibodies in autoimmune heptatitis. Lancet 355: 1475-1476.
26. Obermayer-Straub P, Perheentupa J, Braun S et al. (2001): Hepatic autoantigens in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. Gastroenterology 121: 668-677.
27. Obermayer-Straub P, Strassburg CP, Manns MP (2000): Autoimmune polyglandular syndrome type 1. Clin Rev Allergy Immunol 18: 167-183.
28. Reau, Nancy S; Kalloo, Anthony N (2002): Sclerosing cholangitis. Diagnosis and management Techniques in Gastrointestinal Endoscopy 4: 147-156.
29. Angulo P, Gershwin JB, Eric M, et. al. (2000): Serum autoantibodies in patients with primary sclerosing cholangitis. J Hepatol 32; 182-187.
30. Cullen S, Chapman R (2003): Primary sclerosing cholangitis. Autoimmunity Reviews 2: 305-312.
31. Talwalkar JA, Lindor KD (2003): Primary biliary cirrhosis. Lancet 362: 53-61.
32. Fritzler, Marvin J; Manns, Michael P (2002): Anti-mitochondrial autoantibodies. Clin and Applied Immunology Reviews 3: 87-113.
33. Worman HJ, Courvalin J-C (2003): Antinuclear antibodies specific for primary biliary cirrhosis. Autoimmun Rev 2: 211-217.
Copyright: © 2010 Polish Society of Experimental and Clinical Immunology This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Quick links
© 2019 Termedia Sp. z o.o. All rights reserved.
Developed by Bentus.
PayU - płatności internetowe