Evidence from twins for acquired cellular immune hyperactivity in type 1 diabetes

Immunology. 2002 Aug;106(4):584-9. doi: 10.1046/j.1365-2567.2002.01449.x.

Abstract

Type 1 diabetes has been associated with an increased frequency of activated T cells and T-cell hyperactivity to non-specific and disease-specific stimuli including the islet autoantigen glutamic acid decarboxylase 65 (GAD). To address whether T-cell hyperactivity is genetic or acquired we measured whole blood cytokines in vitro in response to GAD or tetanus in 18 identical twin pairs, nine discordant for type 1 diabetes. In addition, the activity of 2', 5' oligoadenylate synthetase (OAS) in blood mononuclear cells was measured as a marker of viral infection. Interleukin-2 (IL-2) basally and IL-2 and interferon-gamma (IFN-gamma) in response to GAD, were detected more frequently and at higher levels in diabetic compared to non-diabetic twins. IL-10 was not different between groups. OAS activity was increased in diabetic compared to non-diabetic twins and showed a correlation with basal IL-2 and GAD-stimulated IFN-gamma and IL-10. These findings suggest that T-cell hyperactivity in type 1 diabetes is an acquired trait and could reflect persisting virus expression.

Publication types

  • Twin Study

MeSH terms

  • 2',5'-Oligoadenylate Synthetase / blood
  • Autoantigens / immunology
  • Biomarkers / blood
  • Cytokines / biosynthesis
  • Diabetes Mellitus, Type 1 / genetics
  • Diabetes Mellitus, Type 1 / immunology*
  • Diseases in Twins*
  • Glutamate Decarboxylase / immunology
  • Humans
  • Immunity, Cellular
  • Interleukin-2 / biosynthesis
  • Interleukin-2 / blood
  • Registries
  • Tetanus Toxoid / immunology
  • Twins, Monozygotic
  • Virus Diseases / immunology

Substances

  • Autoantigens
  • Biomarkers
  • Cytokines
  • Interleukin-2
  • Tetanus Toxoid
  • 2',5'-Oligoadenylate Synthetase
  • Glutamate Decarboxylase