TCR tuning of T cell subsets

Immunol Rev. 2018 May;283(1):129-137. doi: 10.1111/imr.12646.

Abstract

After selection in the thymus, the post-thymic T cell compartments comprise heterogenous subsets of naive and memory T cells that make continuous T cell receptor (TCR) contact with self-ligands bound to major histocompatibility complex (MHC) molecules. T cell recognition of self-MHC ligands elicits covert TCR signaling and is particularly important for controlling survival of naive T cells. Such tonic TCR signaling is tightly controlled and maintains the cells in a quiescent state to avoid autoimmunity. Here, we review how naive and memory T cells are differentially tuned and wired for TCR sensitivity to self and foreign ligands.

Keywords: CD45; CD5; T cell receptor; TCR tuning; major histocompatibility complex molecules; self-peptides.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • CD5 Antigens / metabolism
  • Cell Differentiation / immunology
  • Histocompatibility Antigens / immunology
  • Histocompatibility Antigens / metabolism
  • Humans
  • Lymphocyte Activation / immunology
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / metabolism*
  • Signal Transduction*
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism*
  • Thymocytes / cytology
  • Thymocytes / immunology
  • Thymocytes / metabolism

Substances

  • CD5 Antigens
  • Histocompatibility Antigens
  • Receptors, Antigen, T-Cell