IRF4 at the crossroads of effector T-cell fate decision

Eur J Immunol. 2014 Jul;44(7):1886-95. doi: 10.1002/eji.201344279. Epub 2014 Jun 16.

Abstract

Interferon regulatory factor 4 (IRF4) is a transcription factor that is expressed in hematopoietic cells and plays pivotal roles in the immune response. Originally described as a lymphocyte-specific nuclear factor, IRF4 promotes differentiation of naïve CD4(+) T cells into T helper 2 (Th2), Th9, Th17, or T follicular helper (Tfh) cells and is required for the function of effector regulatory T (eTreg) cells. Moreover, IRF4 is essential for the sustained differentiation of cytotoxic effector CD8(+) T cells, for CD8(+) T-cell memory formation, and for differentiation of naïve CD8(+) T cells into IL-9-producing (Tc9) and IL-17-producing (Tc17) CD8(+) T-cell subsets. In this review, we focus on recent findings on the role of IRF4 during the development of CD4(+) and CD8(+) T-cell subsets and the impact of IRF4 on T-cell-mediated immune responses in vivo.

Keywords: CD4+ T cells; CD8+ T cells; Interferon regulatory factor 4; T-cell differentiation; T-cell subsets.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Differentiation
  • Humans
  • Interferon Regulatory Factors / chemistry
  • Interferon Regulatory Factors / genetics
  • Interferon Regulatory Factors / physiology*
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology
  • Th1 Cells / cytology
  • Th2 Cells / cytology

Substances

  • Interferon Regulatory Factors
  • interferon regulatory factor-4