Small intestinal T cells of celiac disease patients recognize a natural pepsin fragment of gliadin

Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):10050-4. doi: 10.1073/pnas.95.17.10050.

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

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Celiac Disease / etiology
  • Celiac Disease / immunology*
  • Celiac Disease / pathology
  • Clone Cells
  • Gliadin / chemistry
  • Gliadin / genetics
  • Gliadin / immunology*
  • HLA-DQ Antigens
  • Humans
  • Immunodominant Epitopes / chemistry
  • Immunodominant Epitopes / genetics
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / pathology
  • Intestine, Small / immunology*
  • Intestine, Small / pathology
  • Lymphocyte Activation
  • Molecular Sequence Data
  • Pepsin A
  • Peptide Fragments / chemistry
  • Peptide Fragments / genetics
  • Peptide Fragments / immunology*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / pathology

Substances

  • HLA-DQ Antigens
  • HLA-DQ2 antigen
  • HLA-DQ8 antigen
  • Immunodominant Epitopes
  • Peptide Fragments
  • Gliadin
  • Pepsin A