Cell-specific and context-dependent effects of GITR in cancer, autoimmunity, and infection

Cytokine Growth Factor Rev. 2014 Apr;25(2):91-106. doi: 10.1016/j.cytogfr.2013.12.003. Epub 2014 Jan 4.

Abstract

A breadth of studies have demonstrated the importance of GITR-GITRL in diverse immune processes. However, only a limited number of studies to date have attributed the effects of GITR/GITRL to specific cell types. Moreover, the context-dependent role of GITR/GITRL in different models makes the consequences of GITR ligation difficult to generalize. There is a significant interest in the therapeutic application of GITR agonists and antagonists in human disease. Thus, the field must come to a consensus regarding the cell type-specific and physiological effects of GITR in different disease states. Here we attempt to summarize the extensive literature on GITR, to synthesize a more cohesive picture of the role of GITR/GITRL in immunity, and to identify areas that require clarification.

Keywords: Co-stimulation; GITR; GITRL; T cell; TNFR.

Publication types

  • Review

MeSH terms

  • Animals
  • Autoimmunity / immunology
  • B-Lymphocytes / immunology
  • Cell Adhesion / immunology
  • Communicable Diseases / immunology
  • Dendritic Cells / immunology
  • Glucocorticoid-Induced TNFR-Related Protein / biosynthesis
  • Glucocorticoid-Induced TNFR-Related Protein / immunology*
  • Humans
  • Inflammation / immunology
  • Mice
  • Neoplasms / immunology
  • Signal Transduction / immunology
  • T-Lymphocytes, Regulatory / immunology
  • Tumor Necrosis Factors / biosynthesis
  • Tumor Necrosis Factors / immunology*

Substances

  • Glucocorticoid-Induced TNFR-Related Protein
  • TNFRSF18 protein, human
  • TNFSF18 protein, human
  • Tumor Necrosis Factors