Self-reactive T cells: suppressing the suppressors

Cancer Immunol Immunother. 2014 Apr;63(4):313-9. doi: 10.1007/s00262-013-1512-9. Epub 2013 Dec 25.

Abstract

The immune system is a tightly regulated and complex system. An important part of this immune regulation is the assurance of tolerance toward self-antigens to maintain immune homeostasis. However, in recent years, antigen-specific cellular immune responses toward several normal self-proteins expressed in regulatory immune cells have been reported, especially in patients with cancer. The seemingly lack of tolerance toward such proteins is interesting, as it suggests a regulatory function of self-reactive T (srT) cells, which may be important for the fine tuning of the immune system. In particular, surprising has been the description of cytotoxic srT cells that are able to eliminate normal regulatory immune cells. Such srT cells may be important as effector cells that suppress regulatory suppressor cells. The current knowledge of the nature and function of srT cells is still limited. Still, the therapeutic targeting of srT cells offers a novel approach to harness immune-regulatory networks in cancer.

Publication types

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

MeSH terms

  • Autoantigens / immunology*
  • Autoimmunity / immunology*
  • B7-H1 Antigen / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Cytotoxicity, Immunologic
  • Enzymes / immunology
  • Forkhead Transcription Factors / immunology
  • Gene Rearrangement, T-Lymphocyte / immunology
  • Humans
  • Immune Tolerance / immunology*
  • Models, Immunological
  • Natural Killer T-Cells / immunology
  • Neoplasm Proteins / immunology
  • Receptors, Antigen, T-Cell, alpha-beta / immunology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocytes, Regulatory / immunology
  • Th17 Cells / immunology
  • Tumor Escape / immunology
  • Tumor Microenvironment / immunology

Substances

  • Autoantigens
  • B7-H1 Antigen
  • CD274 protein, human
  • Enzymes
  • Forkhead Transcription Factors
  • Neoplasm Proteins
  • Receptors, Antigen, T-Cell, alpha-beta