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Clinical Immunology |
-enolase Antibodies in Patients with Inflammatory Bowel Disease1 Department of Internal Medicine, University Hospital Leuven;2 Laboratory of Neuroplasticity and Neuroproteomics, Katholieke Universiteit Leuven;3 Department of Laboratory Medicine, University Hospital Leuven;4 Department of Molecular Celbiology, University Hospital Leuven, Leuven, Belgium.
aAddress correspondence to this author at: Laboratory Medicine, University Hospital Gasthuisberg, Herestraat 49-3000 Leuven, Belgium. Fax 32-16-347931; e-mail Xavier.Bossuyt{at}uz.kuleuven.ac.be.
Background: Patients with inflammatory bowel disease (IBD) carry autoantibodies such as perinuclear antineutrophil cytoplasmic antibodies (pANCA).
-Enolase has been proposed as a target antigen in IBD. We evaluated the prevalence and diagnostic value of anti–
-enolase antibodies in IBD and related disorders.
Methods: We used a classic proteomic approach with extracts from granulocytes and pANCA-positive ulcerative colitis (UC) sera to confirm
-enolase as a target antigen. By means of Western blot analysis, we screened a cohort of 525 subjects for the presence of anti–
-enolase antibodies. We performed GeneArray experiments on RNA extracted from colonic mucosal biopsies from 35 IBD and 6 control patients.
Results: We detected anti–
-enolase antibodies 49.0% of patients with UC, 50.0% of patients with Crohns 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
-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–
-enolase antibodies. Preabsorption with
-enolase did not eliminate the pANCA pattern on indirect immunofluorescence.
Conclusions: Anti–
-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–
-enolase antibodies are of limited diagnostic value for the diagnosis of IBD.
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