Effector T cells boost regulatory T cell expansion by IL-2, TNF, OX40, and plasmacytoid dendritic cells depending on the immune context

J Immunol. 2015 Feb 1;194(3):999-1010. doi: 10.4049/jimmunol.1400504. Epub 2014 Dec 29.

Abstract

CD4(+)CD25(+)Foxp3(+) regulatory T (Treg) cells play a major role in peripheral tolerance. Multiple environmental factors and cell types affect their biology. Among them, activated effector CD4(+) T cells can boost Treg cell expansion through TNF or IL-2. In this study, we further characterized this effector T (Teff) cell-dependent Treg cell boost in vivo in mice. This phenomenon was observed when both Treg and Teff cells were activated by their cognate Ag, with the latter being the same or different. Also, when Treg cells highly proliferated on their own, there was no additional Treg cell boost by Teff cells. In a condition of low inflammation, the Teff cell-mediated Treg cell boost involved TNF, OX40L, and plasmacytoid dendritic cells, whereas in a condition of high inflammation, it involved TNF and IL-2. Thus, this feedback mechanism in which Treg cells are highly activated by their Teff cell counterparts depends on the immune context for its effectiveness and mechanism. This Teff cell-dependent Treg cell boost may be crucial to limit inflammatory and autoimmune responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Communication
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism*
  • Immunophenotyping
  • Inflammation / immunology
  • Inflammation / metabolism
  • Interleukin-2 / metabolism*
  • Lymph Nodes / immunology
  • Lymph Nodes / metabolism
  • Lymphocyte Activation / immunology
  • Mice
  • Mice, Transgenic
  • OX40 Ligand / metabolism
  • Phenotype
  • Protein Binding
  • Receptors, OX40 / metabolism*
  • Signal Transduction
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism*
  • Tumor Necrosis Factors / metabolism*

Substances

  • Interleukin-2
  • OX40 Ligand
  • Receptors, OX40
  • Tumor Necrosis Factors