Molecular and cellular insights into T cell exhaustion

Nat Rev Immunol. 2015 Aug;15(8):486-99. doi: 10.1038/nri3862.

Abstract

In chronic infections and cancer, T cells are exposed to persistent antigen and/or inflammatory signals. This scenario is often associated with the deterioration of T cell function: a state called 'exhaustion'. Exhausted T cells lose robust effector functions, express multiple inhibitory receptors and are defined by an altered transcriptional programme. T cell exhaustion is often associated with inefficient control of persisting infections and tumours, but revitalization of exhausted T cells can reinvigorate immunity. Here, we review recent advances that provide a clearer molecular understanding of T cell exhaustion and reveal new therapeutic targets for persisting infections and cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bacterial Infections / immunology*
  • Bacterial Infections / microbiology
  • Bacterial Infections / pathology
  • CD57 Antigens / genetics
  • CD57 Antigens / immunology
  • Clonal Anergy
  • Cytokines / genetics
  • Cytokines / immunology
  • Gene Expression Regulation
  • Humans
  • Immunologic Memory
  • Lymphocyte Activation
  • Neoplasms / immunology*
  • Neoplasms / pathology
  • Signal Transduction
  • T-Lymphocytes, Cytotoxic / immunology*
  • T-Lymphocytes, Cytotoxic / pathology
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / pathology
  • Transcription, Genetic
  • Virus Diseases / immunology*
  • Virus Diseases / pathology
  • Virus Diseases / virology

Substances

  • CD57 Antigens
  • Cytokines