Abstract
Celiac disease is a common severe intestinal disease resulting from intolerance to dietary wheat gluten and related proteins. The large majority of patients expresses the HLA-DQ2 and/or DQ8 molecules, and gluten-specific HLA-DQ-restricted T cells have been found at the site of the lesion in the gut. The nature of peptides that are recognized by such T cells, however, has been unclear so far. We now report the identification of a gliadin-derived epitope that dominantly is recognized by intestinal gluten-specific HLA-DQ8-restricted T cells. The characterization of such epitopes is a key step toward the development of strategies to interfere in mechanisms involved in the pathogenesis of celiac disease.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Celiac Disease / etiology
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Celiac Disease / immunology*
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Celiac Disease / pathology
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Clone Cells
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Gliadin / chemistry
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Gliadin / genetics
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Gliadin / immunology*
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HLA-DQ Antigens
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Humans
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Immunodominant Epitopes / chemistry
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Immunodominant Epitopes / genetics
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Intestinal Mucosa / immunology
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Intestinal Mucosa / pathology
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Intestine, Small / immunology*
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Intestine, Small / pathology
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Lymphocyte Activation
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Molecular Sequence Data
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Pepsin A
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Peptide Fragments / chemistry
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Peptide Fragments / genetics
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Peptide Fragments / immunology*
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T-Lymphocytes / immunology*
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T-Lymphocytes / pathology
Substances
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HLA-DQ Antigens
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HLA-DQ2 antigen
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HLA-DQ8 antigen
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Immunodominant Epitopes
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Peptide Fragments
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Gliadin
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Pepsin A