CD40-CD40Ligand interactions and their role in cytotoxic T lymphocyte priming and anti-tumor immunity

Semin Immunol. 1998 Dec;10(6):443-8. doi: 10.1006/smim.1998.0147.

Abstract

Tumor-specific immunity relies on interactions with the antigen receptors as well as costimulatory molecules, such as those of the CD28/B7 pathway and relatives of the TNFR gene family. Cytotoxic T lymphocytes specific for cellular antigens are in general primed by professional antigen-presenting cells that indirectly present antigens derived from cells in the periphery. This cross-priming of CD8(+) T cells requires signals provided by CD4(+) T helper cells. Although this dependency on [help' for efficient cytotoxic T lymphocyte priming has been well documented, it was only recently that more mechanistic insight into the nature of this event has been obtained. In the absence of the CD4(+) T cells, signalling through CD40 can replace 'help' required for priming of these CD8(+) T cells. These observations indicate that T cell help for cytotoxic T lymphocytes is mediated by CD40-CD40Ligand (L) interactions, most likely through activation of professional antigen-presenting cells that cross-present cellular antigens to these T cells.

Publication types

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

MeSH terms

  • Animals
  • Antigen-Presenting Cells / immunology
  • Antigens, Neoplasm / immunology*
  • CD4-Positive T-Lymphocytes / immunology
  • CD40 Antigens / immunology*
  • CD40 Antigens / metabolism*
  • CD40 Ligand
  • CD8-Positive T-Lymphocytes / immunology
  • Humans
  • Lymphocyte Activation
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / metabolism*
  • T-Lymphocytes, Cytotoxic / immunology*
  • T-Lymphocytes, Helper-Inducer / immunology

Substances

  • Antigens, Neoplasm
  • CD40 Antigens
  • Membrane Glycoproteins
  • CD40 Ligand