潘卡
医学
抗中性粒细胞胞浆抗体
溃疡性结肠炎
自身抗体
炎症性肠病
抗体
免疫学
胃肠病学
烯醇化酶
原发性硬化性胆管炎
自身免疫性肝炎
内科学
血管炎
疾病
肝炎
免疫组织化学
作者
Nathalie Vermeulen,Ingrid Arijs,Sofie Joossens,Séverine Vermeire,Stefan Clerens,K. Van den Bergh,G Michiels,Lut Arckens,Frans Schuit,Leentje Van Lommel,Paul Rutgeerts,Xavier Bossuyt
出处
期刊:Clinical Chemistry
[American Association for Clinical Chemistry]
日期:2008-01-25
卷期号:54 (3): 534-541
被引量:49
标识
DOI:10.1373/clinchem.2007.098368
摘要
Patients with inflammatory bowel disease (IBD) carry autoantibodies such as perinuclear antineutrophil cytoplasmic antibodies (pANCA). alpha-Enolase has been proposed as a target antigen in IBD. We evaluated the prevalence and diagnostic value of anti-alpha-enolase antibodies in IBD and related disorders.We used a classic proteomic approach with extracts from granulocytes and pANCA-positive ulcerative colitis (UC) sera to confirm alpha-enolase as a target antigen. By means of Western blot analysis, we screened a cohort of 525 subjects for the presence of anti-alpha-enolase antibodies. We performed GeneArray experiments on RNA extracted from colonic mucosal biopsies from 35 IBD and 6 control patients.We detected anti-alpha-enolase antibodies 49.0% of patients with UC, 50.0% of patients with Crohn's disease, 30.5% of patients with primary sclerosing cholangitis, 37.8% of patients with autoimmune hepatitis, 34.0% of patients with ANCA-positive vasculitis, 31.0% of non-IBD gastrointestinal controls, and 8.5% of healthy controls. Gene array experiments showed a significant upregulation of alpha-enolase mRNA in colonic mucosal biopsies from patients with IBD, but not from controls. There was no association between the presence of pANCA and anti-alpha-enolase antibodies. Preabsorption with alpha-enolase did not eliminate the pANCA pattern on indirect immunofluorescence.Anti-alpha-enolase antibodies are present in a substantial proportion of patients with IBD, patients with various inflammatory/autoimmune disorders, and non-IBD gastrointestinal controls. Therefore, anti-alpha-enolase antibodies are of limited diagnostic value for the diagnosis of IBD.
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