T-cell receptor affinity in the age of cancer immunotherapy

Mol Carcinog. 2020 Jul;59(7):862-870. doi: 10.1002/mc.23212. Epub 2020 May 9.

Abstract

The strength of the interaction between T-cell receptors (TCRs) and their ligands, peptide/major histocompatibility complex complexes (pMHCs), is one of the most frequently discussed and investigated features of T cells in immuno-oncology today. Although there are many molecules on the surface of T cells that interact with ligands on other cells, the TCR/pMHC is the only receptor-ligand pair that offers antigen specificity and dictates the functional response of the T cell. The strength of the TCR/pMHC interaction, along with the environment in which this interaction takes place, is key to how the T cell will respond. The TCR repertoire of T cells that interact with tumor-associated antigens is vast, although typically of low affinity. Here, we focus on the low-affinity interactions between TCRs from CD8+ T cells and different models used in immuno-oncology.

Keywords: CD8+ T cells; TCR-pMHC affinity; altered peptide ligands; low affinity; tumor antigens.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology
  • Histocompatibility Antigens / immunology
  • Humans
  • Immunotherapy / methods
  • Neoplasms / immunology*
  • Neoplasms / therapy*
  • Receptors, Antigen, T-Cell / immunology*

Substances

  • Histocompatibility Antigens
  • Receptors, Antigen, T-Cell