Cutting edge: CD95 maintains effector T cell homeostasis in chronic immune activation

J Immunol. 2005 May 15;174(10):5915-20. doi: 10.4049/jimmunol.174.10.5915.

Abstract

The elimination of activated T cells is important to maintain homeostasis and avoid immunopathology. CD95 (Fas/APO-1) has been identified as a death mediator for activated T cells in vitro but the function of CD95 in death of mature T cells in vivo is still controversial. Here we show that triggering of the costimulatory TNF receptor family member CD27 sensitized T cells for CD95-induced apoptosis. CD95-deficient (lpr/lpr) T cells massively expanded and differentiated into IFN-gamma-secreting effector cells in transgenic mice that constitutively express the CD27 ligand, CD70. Concomitantly, CD95-deficient CD70 transgenic mice became moribund by 4 wk of age with severe liver pathology and bone marrow failure. These findings establish that CD95 is a critical regulator of effector T cell homeostasis in chronic immune activation.

MeSH terms

  • Adoptive Transfer
  • Animals
  • Animals, Newborn
  • Antigens, CD / genetics
  • Antigens, CD / physiology
  • Apoptosis / genetics
  • Apoptosis / immunology
  • CD27 Ligand
  • CD8-Positive T-Lymphocytes / cytology*
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • Cell Death / genetics
  • Cell Death / immunology
  • Cell Differentiation / genetics
  • Cell Differentiation / immunology
  • Gene Deletion
  • Homeostasis / genetics
  • Homeostasis / immunology*
  • Interferon-gamma / metabolism
  • Interferon-gamma / pharmacology
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology*
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred MRL lpr
  • Mice, Knockout
  • Mice, Transgenic
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocyte Subsets / pathology
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / pharmacology
  • fas Receptor / genetics
  • fas Receptor / physiology*

Substances

  • Antigens, CD
  • CD27 Ligand
  • Cd70 protein, mouse
  • Membrane Proteins
  • Tumor Necrosis Factor Receptor Superfamily, Member 7
  • fas Receptor
  • Interferon-gamma