Block of both TGF-β and IL-2 signaling impedes Neurophilin-1+ regulatory T cell and follicular regulatory T cell development

Cell Death Dis. 2016 Oct 27;7(10):e2439. doi: 10.1038/cddis.2016.348.

Abstract

Understanding the mechanisms that lead to autoimmunity is critical for defining potential therapeutic pathways. In this regard there have been considerable efforts in investigating the interacting roles of TGF-β and IL-2 on the function regulatory T cells. We have taken advantage of dnTGF-βRII Il2ra-/- (abbreviated as Il2ra-/-Tg) mouse model, which allows a direct mechanistic approach to define the relative roles of TGF-β and IL-2 on Treg development. Il2ra-/-Tg mice spontaneously developed multi-organ autoimmune diseases with expansion of pathogenic T cells and enhanced germinal center response at 3-4 weeks of age. Importantly, peripheral Treg cells from Il2ra-/-Tg mice demonstrated an activated Th1-like stable phenotype and normal in vitro suppressive function, while thymus Treg increased but manifested decreased suppressive function. Interestingly, neither thymus nor peripheral Treg cells of Il2ra-/-Tg mice contained Neuropilin-1+ or PD-1hi phenotype, resulting in defective follicular regulatory T (Tfr) cell development. Such defective Tfr development led to elevated follicular T helper cells, enhanced germinal center responses and increased plasma cell infiltration. These data demonstrate an important synergetic role of TGF-β and IL-2 in the generation, activation and stability of Treg cells, as well as their subsequent development into Tfr cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Germinal Center / metabolism
  • Immunophilins / metabolism*
  • Inflammation / pathology
  • Interleukin-2 / metabolism*
  • Interleukin-2 Receptor alpha Subunit / metabolism
  • Lymphadenopathy / pathology
  • Lymphocyte Activation / immunology
  • Mice, Transgenic
  • Phenotype
  • Signal Transduction*
  • T-Lymphocytes, Helper-Inducer / cytology
  • T-Lymphocytes, Regulatory / metabolism*
  • Transforming Growth Factor beta / metabolism*

Substances

  • Interleukin-2
  • Interleukin-2 Receptor alpha Subunit
  • Transforming Growth Factor beta
  • Immunophilins