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Binding of peptides from the N-terminal region of alpha-gliadin to the celiac disease-associated HLA-DQ2 molecule assessed in biochemical and T cell assays
Author(s): Johansen BH, Gjertsen HA, Vartdal F, Buus S, Thorsby E, Lundin KEA, Sollid LM
Source: CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY    Volume: 79    Issue: 3    Pages: 288-293    Published: JUN 1996  
Times Cited: 25     References: 23     
Abstract: Celiac disease (CD) is most probably an immunological disease, precipitated in susceptible individuals by ingestion of wheat gliadin and related proteins from other cereals. The disease shows a strong HLA association predominantly to the cis- or trans-encoded HLA-DQ(alpha 1*0501, beta 1*02) (i.e., DQ2) heterodimer. T cell recognition of gliadin peptides presented by DQ2 in the intestinal mucosa is central in the immunopathogenesis of CD. Here we describe a study where overlapping peptides from the N-terminal region of alpha-gliadin have been tested in biochemical assays for binding to affinity-purified DQ2 and DR3 (i.e., DR(alpha, beta 1*0301)) molecules. The peptides were also tested for binding to DQ2 in a functional binding assay, where binding was measured as the capacity to inhibit the stimulation of a gliadin-specific, DQ2-restricted T lymphocyte clone RNnT alpha 33. In both assay systems the overlapping gliadin peptides were found to bind with weak or intermediate affinity to DQ2. No or only very weak binding was found to DR3 in the biochemical binding assay. Overall, the results question the role of these peptides in the T-cell-mediated immunopathogenesis of CD. The in vitro assays described here provide new methods for the screening of potentially toxic peptides. (C) 1996 Academic Press, Inc.
Document Type: Article
Language: English
Reprint Address: Johansen, BH (reprint author), UNIV OSLO, NATL HOSP, INST TRANSPLANTAT IMMUNOL, N-0027 OSLO, NORWAY
Addresses:
1. UNIV COPENHAGEN, INST MED MICROBIOL & IMMUNOL, COPENHAGEN, DENMARK
Publisher: ACADEMIC PRESS INC JNL-COMP SUBSCRIPTIONS, 525 B ST, STE 1900, SAN DIEGO, CA 92101-4495
Subject Category: Immunology; Pathology
IDS Number: UM794
ISSN: 0090-1229
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