The fidelity, occasional promiscuity, and versatility of T cell receptor recognition

Immunity. 2008 Mar;28(3):304-14. doi: 10.1016/j.immuni.2008.02.004.

Abstract

Although there are multiple structures showing how alphabeta T cell receptors (TCRs) specifically recognize antigenic peptides bound to the major histocompatibility complex (MHC) molecules (pMHC-I and pMHC-II), we have little data on how TCRs interact with lipid-based antigens presented by members of the CD1 family. Here, we review recent findings in the field of TCR recognition, including TCR-pMHC complexes and the structure of a TCR in complex with CD1d-glycolipid. Collectively, these studies have revealed the versatility of the TCR in recognizing the distinct yet evolutionarily related proteinaceous and lipid-presenting molecules of the immune system.

Publication types

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

MeSH terms

  • Animals
  • Antigen Presentation / immunology*
  • Antigens, CD1 / immunology
  • Antigens, CD1d
  • Glycolipids / immunology
  • Humans
  • Lymphocyte Activation / immunology*
  • Major Histocompatibility Complex / immunology
  • Receptors, Antigen, T-Cell / immunology*
  • Receptors, Antigen, T-Cell / metabolism
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • Antigens, CD1
  • Antigens, CD1d
  • CD1D protein, human
  • Glycolipids
  • Receptors, Antigen, T-Cell