Article (Scientific journals)
Identification of a novel autoantigen in inflammatory bowel disease by protein microarray.
Vermeulen, Nathalie; de Beeck, Katrijn Op; Vermeire, Severine et al.
2011In Inflammatory Bowel Diseases, 17 (6), p. 1291-300
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Keywords :
Autoantigens/immunology; Blotting, Western; Case-Control Studies; Colitis, Ulcerative/immunology; Crohn Disease/immunology; Female; Humans; Inflammatory Bowel Diseases/immunology; Male; Middle Aged; Protein Array Analysis
Abstract :
[en] BACKGROUND: Patients with inflammatory bowel disease (IBD) display immunoreactivity to self-antigens and microbial antigens. We used a protein microarray approach to identify novel autoantigens in IBD. METHODS: ProtoArray Human Protein Microarray v4.0 containing 8268 human proteins from Invitrogen (La Jolla, CA) was used. RESULTS: Twenty-five IBD patients and five healthy controls were screened for candidate autoantigens. For 256 antigens, IBD patients had a higher seroreactivity than controls. Twenty antigens were selected for further evaluation in a larger cohort (60 ulcerative colitis [UC] patients, 60 Crohn's disease [CD] patients, 60 healthy controls, and 60 gastrointestinal-diseased controls) by means of a customized protein microarray. Out of these 20 antigens, one antigen, family with sequence similarity 84 member A (FAM84A), was identified as a target antigen in IBD. Antibodies to FAM84A were significantly more prevalent in IBD patients (19%) than in gastrointestinal-diseased controls (1.7%) (P = 0.0008) and healthy controls (5%) (P = 0.01). Anti-FAM84A antibodies were found in 26.6% of UC patients and in 11.7% of CD patients. FAM84A was confirmed as target antigen in IBD by means of Western blotting in a large independent cohort (100 UC patients, 106 CD patients, 102 healthy controls, and 100 gastrointestinal-diseased controls). Antibodies to FAM84A were significantly more prevalent in IBD patients (20%) than in gastrointestinal-diseased controls (5%) (P = 0.0004) and healthy controls (0%) (P < 0.0001). Anti-FAM84A antibodies were found in 18% of UC patients and in 22% of CD patients. CONCLUSIONS: We identified FAM84A as a novel autoantigen in IBD. (Inflamm Bowel Dis 2011;).
Disciplines :
Gastroenterology & hepatology
Author, co-author :
Vermeulen, Nathalie
de Beeck, Katrijn Op
Vermeire, Severine
Van Steen, Kristel  ;  Université de Liège - ULiège > Dép. d'électric., électron. et informat. (Inst.Montefiore) > Bioinformatique
Michiels, Georges
Ballet, Vera
Rutgeerts, Paul
Bossuyt, Xavier
Language :
English
Title :
Identification of a novel autoantigen in inflammatory bowel disease by protein microarray.
Publication date :
2011
Journal title :
Inflammatory Bowel Diseases
ISSN :
1078-0998
eISSN :
1536-4844
Publisher :
Lippincott Williams & Wilkins, Hagerstown, United States - Maryland
Volume :
17
Issue :
6
Pages :
1291-300
Peer reviewed :
Peer Reviewed verified by ORBi
Commentary :
Copyright (c) 2010 Crohn's & Colitis Foundation of America, Inc.
Available on ORBi :
since 01 November 2011

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