Expanded T cells from pancreatic lymph nodes of type 1 diabetic subjects recognize an insulin epitope

Nature. 2005 May 12;435(7039):224-8. doi: 10.1038/nature03625.

Abstract

In autoimmune type 1 diabetes, pathogenic T lymphocytes are associated with the specific destruction of insulin-producing beta-islet cells. Identification of the autoantigens involved in triggering this process is a central question. Here we examined T cells from pancreatic draining lymph nodes, the site of islet-cell-specific self-antigen presentation. We cloned single T cells in a non-biased manner from pancreatic draining lymph nodes of subjects with type 1 diabetes and from non-diabetic controls. A high degree of T-cell clonal expansion was observed in pancreatic lymph nodes from long-term diabetic patients but not from control subjects. The oligoclonally expanded T cells from diabetic subjects with DR4, a susceptibility allele for type 1 diabetes, recognized the insulin A 1-15 epitope restricted by DR4. These results identify insulin-reactive, clonally expanded T cells from the site of autoinflammatory drainage in long-term type 1 diabetics, indicating that insulin may indeed be the target antigen causing autoimmune diabetes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Case-Control Studies
  • Clone Cells / cytology
  • Clone Cells / immunology
  • Diabetes Mellitus, Type 1 / immunology*
  • Diabetes Mellitus, Type 1 / pathology
  • Epitopes, T-Lymphocyte / immunology*
  • HLA-DR Antigens / immunology
  • HLA-DRB1 Chains
  • Humans
  • Insulin / immunology*
  • Lymph Nodes / cytology
  • Lymph Nodes / immunology*
  • Molecular Sequence Data
  • Pancreas / immunology*
  • Receptors, Antigen, T-Cell / chemistry
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / immunology
  • Substrate Specificity
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology*

Substances

  • Epitopes, T-Lymphocyte
  • HLA-DR Antigens
  • HLA-DRB1 Chains
  • Insulin
  • Receptors, Antigen, T-Cell