A T cell extrinsic mechanism by which IL-2 dampens Th17 differentiation

J Autoimmun. 2015 May:59:38-42. doi: 10.1016/j.jaut.2015.02.001. Epub 2015 Feb 26.

Abstract

Genetic variants in il2 and il2ra have been associated with autoimmune disease susceptibility in both genome-wide association studies (GWAS) in humans and in genetic linkage studies in experimental models of autoimmunity. Specifically, genetic variants resulting in a low IL-2 phenotype are susceptibility alleles while variants resulting in a high IL-2 phenotype are resistance alleles. The association of high IL-2 phenotypes with resistance has been attributed primarily to the T cell intrinsic promotion of regulatory T cell development, maintenance, and function; however, IL-2 can also act T cell intrinsically to dampen differentiation of pathogenic IL-17-producing Th17 cells. Here, we have uncovered a novel T cell extrinsic mechanism whereby IL-2 promotes both IFN-γ and IL-27 production from tissue resident macrophages which in turn dampen the differentiation of pathogenic Th17 cells.

Keywords: Cytokines; IL-17; Macrophages; T cells.

Publication types

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

MeSH terms

  • Animals
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology*
  • Cell Differentiation
  • Cells, Cultured
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Interferon-gamma / metabolism
  • Interleukin-2 / genetics
  • Interleukin-2 / metabolism*
  • Interleukin-27 / metabolism
  • Macrophages / immunology*
  • Mice
  • Mice, Inbred NOD
  • Models, Animal
  • Polymorphism, Genetic
  • T-Lymphocyte Subsets / immunology*
  • Th17 Cells / immunology*

Substances

  • Interleukin-2
  • Interleukin-27
  • Interferon-gamma