Beyond Cell Death: New Functions for TNF Family Cytokines in Autoimmunity and Tumor Immunotherapy

Trends Mol Med. 2018 Jul;24(7):642-653. doi: 10.1016/j.molmed.2018.05.004. Epub 2018 Jun 4.

Abstract

Originally discovered as an inducer of apoptosis, the TNF-family receptor Fas (CD95, APO-1, TNFRSF6) has more recently been found to have functions beyond cell death, including T cell co-stimulation and promoting terminal differentiation of CD4+ and CD8+ T cells. Other TNF family members also discovered as apoptosis inducers, such as TRAIL (APO-2L, TNFSF10), can promote inflammation through caspase-8. Surprisingly, non-apoptotic signaling through Fas can protect from the autoimmunity seen in Fas deficiency independently from the cell death inducing functions of the receptor. Non-apoptotic Fas signaling can induce tumor cell growth and migration, and impair the efficacy of T cell adoptive immunotherapy. Blocking of non-apoptotic functions of these receptors may be a novel strategy to regulate autoimmunity and inflammation, and enhance antitumor immunity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Autoimmunity / physiology*
  • Cell Death / physiology*
  • Cell Proliferation / physiology
  • Cytokines / metabolism*
  • Humans
  • Immunotherapy / methods
  • Neoplasms / immunology
  • Neoplasms / metabolism*
  • Neoplasms / therapy*
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Cytokines
  • Tumor Necrosis Factor-alpha