Abstract
Aim The aim of this study was to evaluate, retrospectively, the frequency of anti-Saccharomyces cerevisiae antibodies (ASCA) in patients with primary biliary cirrhosis (PBC). Methods ASCA, IgG, and IgA, were determined by ELISA in sera of 95 PBC patients; 80 healthy blood donors served as controls. Results The frequency of ASCA (IgG or IgA) was significantly higher in PBC patients than in the control group (24.2% vs 3.7%, P = 0.0001). The frequency of ASCA IgG and ASCA IgA in PBC patients was also significantly higher than that found in the control group (18.9% vs 2.5%, P = 0.0006 and 11.6% vs 1.2%, P = 0.007, respectively). Six patients out of 95 (6.3%) had both ASCA IgG and ASCA IgA; in contrast, none of the control group had both isotypes (P = 0.02). There was no correlation between ASCA levels and mitochondrial autoantibodies (AMA) titres in PBC patients. Conclusion We conclude that ASCA are common in patients with PBC.
Similar content being viewed by others
References
Kaplan MM, Gershwin ME (2005) Primary biliary cirrhosis. N Engl J Med 353:1261–1273
Quinton JF, Sendid B, Reumaux D, Duthilleul P, Cortot A, Grandbastien B, Charrier G, Targan SR, Colombel JF, Poulain D (1998) Anti-Saccharomyces cerevisiae mannan antibodies combined with antineutrophil cytoplasmic autoantibodies in inflammatory bowel disease: prevalence and diagnostic role. Gut 42:788–791
Toumi D, Mankaï A, Belhadj R, Ghedira-Besbes L, Jeddi M, Ghedira I (2007) Anti-Saccharomyces cerevisiae antibodies in coeliac disease. Scand J Gastroenterol 42:821–826
Mallant-Hent RCh, Mary B, von Blomberg E, Yuksel Z, Wahab PJ, Gundy C, Meyer GA, Mulder CJ (2006) Disappearance of anti-Saccharomyces cerevisiae antibodies in coeliac disease during a gluten-free diet. Eur J Gastroenterol Hepatol 18:75–78
Granito A, Zauli D, Muratori P, Muratori L, Grassi A, Bortolotti R, Petrolini N, Veronesi L, Gionchetti P, Bianchi FB, Volta U (2005) Anti-Saccharomyces cerevisiae and perinuclear anti-neutrophil cytoplasmic antibodies in coeliac disease before and after gluten-free diet. Aliment Pharmacol Ther 21:881–887
Candelli M, Nista EC, Carloni E, Pignataro G, Rigante D, Gasbarrini A (2003) Anti-Saccharomyces cerevisiae antibodies and coeliac disease. Scand J Gastroenterol 38:1191–1192
Damoiseaux JG, Bouten B, Linders AM, Austen J, Roozendaal C, Russel MG, Forget PP, Tervaert JW (2002) Diagnostic value of anti-Saccharomyces cerevisiae and antineutrophil cytoplasmic antibodies for inflammatory bowel disease: high prevalence in patients with celiac disease. J Clin Immunol 22:281–288
Reddy KR, Colombel JF, Poulain D, Krawitt EL (2001) Anti-Saccharomyces cerevisiae antibodies in autoimmune liver disease. Am J Gastroenterol 96:252–253
Muratori P, Muratori L, Guidi M, Maccariello S, Pappas G, Ferrari R, Gionchetti P, Campieri M, Bianchi FB (2003) Anti-Saccharomyces cerevisiae antibodies (ASCA) and autoimmune liver diseases. Clin Exp Immunol 132:473–476
Czaja AJ, Shums Z, Donaldson PT, Norman GL (2004) Frequency and significance of antibodies to Saccharomyces cerevisiae in autoimmune hepatitis. Dig Dis Sci 49:611–618
Krause I, Monselise Y, Milo G, Weinberger A (2002) Anti-Saccharomyces cerevisiae antibodies a novel serologic marker for Behcet’s disease. Clin Exp Rheumatol 20(4 Suppl 26):S21–S24
Torok HP, Glas J, Gruber R, Brumberger V, Strasser C, Kellner H, Marker-Hermann E, Folwaczny C (2004) Inflammatory bowel disease-specific autoantibodies in HLA-B27-associated spondyloarthropathies: increased prevalence of ASCA and pANCA. Digestion 70:49–54
Makharia GK, Sachdev V, Gupta R, Lal S, Pandey RM (2007) Anti-saccharomyces cerevisiae antibody does not differentiate between Crohn’s disease and intestinal tuberculosis. Dig Dis Sci 52:33–39
Bargou I, Mankaï A, Jamaa A, Ben Jazia I, Skandrani K, Sfar H, Baccouche A, Ajmi S, Letaief A, Fabien N, Jeddi M, Ghedira I (2007) Detection of M2 antimitochondrial antibodies by dot blot assay is more specific than by enzyme linked immunosorbent assay. Pathol Biol (Paris) (in press) doi:10.1016/j.patbio2007.05.001
D’Inca R, Annese V, di Leo V, Latiano A, Quaino V, Abazia C, Vettorato MG, Sturniolo GC (2006) Increased intestinal permeability and NOD2 variants in familial and sporadic Crohn’s disease. Aliment Pharmacol Ther 23:1455–1461
Duerksen DR, Wilhelm-Boyles C, Parry DM (2005) Intestinal permeability in long-term follow-up of patients with celiac disease on a gluten-free diet. Dig Dis Sci 50:785–790
Fresko I, Hamuryudan V, Demir M, Hizli N, Sayman H, Melikoglu M, Tunc R, Yurdakul S, Yazici H (2001) Intestinal permeability in Behcet’s syndrome. Ann Rheum Dis 60:65–66
Vaile JH, Meddings JB, Yacyshyn BR, Russell AS, Maksymowych WP (1999) Bowel permeability and CD45RO expression on circulating CD20+ B cells in patients with ankylosing spondylitis an their relatives. J Rheumatol 26:128–135
Di Leo V, Venturi C, Baragiotta A, Martines D, Floreani A (2003) Gastroduodenal and intestinal permeability in primary biliary cirrhosis. Eur J Gastroenterol Hepatol 15:967–973
Feld JJ, Meddings J, Heathcote EJ (2006) Abnormal intestinal permeability in primary biliary cirrhosis. Dig Dis Sci 51:1607–1613
Teoh KL, Mackay IR, Rowley MJ, Fussey SP (1994) Enzyme inhibitory autoantibodies to pyruvate dehydrogenase complex in primary biliary cirrhosis differ for mammalian, yeast and bacterial enzymes: implications for molecular mimicry. Hepatology 19:1029–1033
Cabiscol E, Piulats E, Echave P, Herrero E, Ros J (2000) Oxidative stress promotes specific protein damage in Saccharomyces cerevisiae. J Biol Chem 275:27393–27398
Fasano A (2006) Systemic autoimmune disorders in celiac disease. Curr Opin Gastroenterol 22:674–679
Fasano A, Shea-Donohue T (2005) Mechanisms of disease: the role of intestinal barrier function in the pathogenesis of gastrointestinal autoimmune diseases. Nat Clin Pract Gastroenterol Hepatol 2:416–422
Watts T, Berti I, Sapone A, Gerarduzzi T, Not T, Zielke R, Fasano A (2005) Role of the intestinal tight junction modulator zonulin in the pathogenesis of type I diabetes in BB diabetic-prone rats. Proc Natl Acad Sci 102:2916–2921
Sendid B, Quinton JF, Charrier G, Goulet O, Cortot A, Grandbastien B, Poulain D, Colombel JF (1998) Anti-Saccharomyces cerevisiae mannan antibodies in familial Crohn’s disease. Am J Gastroenterol 93:1306–1310
Monselise A, Weinberger A, Monselise Y, Fraser A, Sulkes J, Krause I (2006) Anti-Saccharomyces cerevisiae antibodies in Behcet’s disease—a familial study. Clin Exp Rheumatol 24(5 Suppl 42):S087–S090
Acknowledgement
This study is supported by the Research Unit of Auto-immunity and Allergy (03UR/07-02), Faculty of Pharmacy, Monastir, Tunisia.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Sakly, W., Jeddi, M. & Ghedira, I. Anti-Saccharomyces cerevisiae Antibodies in Primary Biliary Cirrhosis. Dig Dis Sci 53, 1983–1987 (2008). https://doi.org/10.1007/s10620-007-0092-y
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10620-007-0092-y