Deleting islet autoimmunity

Cell Biochem Biophys. 2007;48(2-3):177-82. doi: 10.1007/s12013-007-0022-9.

Abstract

Even though there are numerous autoantigens for type 1 diabetes, current evidence suggests that a single autoantigen, namely insulin, is responsible for the key initiating event in autoimmunity. If a single autoantigen is necessary for triggering the autoimmune process, then antigen-specific therapy to block or delete the immune response against that autoantigen before epitope spreading occurs, may become a larger focus of future immunotherapeutic strategies. In this article, we review current literature regarding insulin as an autoantigen and potential approaches to deleting insulin-reactive T cells through the use of peptide vaccines and targeted T cell receptor immunizations.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Autoantigens / immunology
  • Autoimmunity / immunology*
  • Diabetes Mellitus, Type 1 / immunology*
  • Diabetes Mellitus, Type 1 / therapy
  • Epitopes, T-Lymphocyte / immunology
  • Immunotherapy
  • Insulin / immunology*
  • Islets of Langerhans / immunology*
  • Peptide Fragments / immunology
  • T-Lymphocytes / immunology

Substances

  • Autoantigens
  • Epitopes, T-Lymphocyte
  • Insulin
  • Peptide Fragments
  • insulin B (9-23)