Apportioning Blame: Autoreactive CD4+ and CD8+ T Cells in Type 1 Diabetes

Arch Immunol Ther Exp (Warsz). 2017 Aug;65(4):275-284. doi: 10.1007/s00005-016-0452-4. Epub 2017 Jan 12.

Abstract

Type 1 diabetes (T1D) is one of the most studied archetypal organ-specific autoimmune diseases. Although many clinical, epidemiological, and pathological characteristics have been described, there are still important issues which need to be resolved as these will have a major impact on the development of future antigen-specific immunotherapies. An important question relates to T lymphocytes in the development of the disease, in particular their role in the destruction of insulin-producing beta cells. Since the discovery that certain class II histocompatibility complex molecules (HLA) are linked to the development of T1D, much research has focused on CD4+ helper T lymphocytes; however, recent studies highlight class I HLA molecules as an independent risk factor; hence, research into the role played by CD8+ cytotoxic T lymphocytes has gained momentum. In this review, we summarize recent studies clarifying the role played by both sets of autoreactive T lymphocytes in T1D, discuss the targets recognized by these cells and their phenotype in T1D patients. Finally, we will examine the possible generation of regulatory CD8+ T lymphocytes upon different immuno-intervention strategies.

Keywords: Autoantigens; CD8; Regulatory T cells; T lymphocytes; Type 1 diabetes.

Publication types

  • Review

MeSH terms

  • Animals
  • Autoantigens / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • Diabetes Mellitus, Type 1 / genetics
  • Diabetes Mellitus, Type 1 / immunology*
  • HLA Antigens / genetics*
  • Humans
  • Immunomodulation
  • Insulin / metabolism*
  • Insulin-Secreting Cells / immunology*
  • Polymorphism, Genetic
  • T-Lymphocytes, Regulatory / immunology*

Substances

  • Autoantigens
  • HLA Antigens
  • Insulin