Regulation of CD8(+) T cell functions by RARgamma

Semin Immunol. 2009 Feb;21(1):2-7. doi: 10.1016/j.smim.2008.07.002. Epub 2008 Aug 20.

Abstract

Retinoic acid plays a key role in the development and function of the immune system; however, the contribution of each of the three retinoic acid receptors (RARs) to the T cell immune response is not yet well understood. Of these receptors, both RARalpha and RARgamma are expressed in T lymphocytes. While possible functional redundancy thus complicates understanding of the role of each receptor in T cells, emerging data suggest that RARalpha and RARgamma function differently in thymocyte development and that RARgamma is required for both primary and secondary CD8(+) T cell immune responses.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / immunology
  • Antineoplastic Agents / metabolism
  • Apoptosis / physiology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • Gastrointestinal Tract / immunology
  • Gastrointestinal Tract / metabolism
  • Humans
  • Receptors, Retinoic Acid / immunology
  • Receptors, Retinoic Acid / metabolism*
  • Retinoic Acid Receptor gamma
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism
  • Tretinoin / immunology*
  • Tretinoin / metabolism

Substances

  • Antineoplastic Agents
  • Receptors, Retinoic Acid
  • Tretinoin