The role of CD97 in regulating adaptive T-cell responses

Adv Exp Med Biol. 2010:706:138-48. doi: 10.1007/978-1-4419-7913-1_12.

Abstract

CD97 was identified as an early activation marker on T cells, having low expression on naive T cells. This is a common feature of molecules that have a role in T-cell function. It was subsequently identified as a ligand for CD55, which has been previously identified as an innate regulator of complement. The interaction of this receptor-ligand pair has been shown to provide a potent costimulatory signal to human T cells, despite their modest affinity. Though both CD97 and CD55 are expressed on T cells as well as antigen presenting cells (APCs), their interaction is significant when CD97 on APCs interacts with CD55 on T cells. The converse interaction is poorly defined and may be less significant. A unique aspect of the interaction of CD97 with CD55 is the stimulation of naive T cells, leading to the induction of IL-10 producing cells that behave like Trl regulatory cells. This raises a number of questions regarding the dual functions of CD55; regulating complement and stimulating T cells via CD97 interaction and any potential overlap in the consequences of these dual roles.

Publication types

  • Review

MeSH terms

  • Adaptive Immunity*
  • Animals
  • Antigens, CD / chemistry
  • Antigens, CD / immunology*
  • Biomarkers / metabolism
  • CD55 Antigens / immunology
  • Complement System Proteins / immunology
  • Humans
  • Lymphocyte Activation
  • Lymphocyte Subsets / immunology
  • Models, Molecular
  • Protein Conformation
  • Receptors, G-Protein-Coupled
  • Signal Transduction / physiology
  • T-Lymphocytes / immunology*

Substances

  • ADGRE5 protein, human
  • Antigens, CD
  • Biomarkers
  • CD55 Antigens
  • Receptors, G-Protein-Coupled
  • Complement System Proteins