Structure and function of programmed death (PD) molecules

Vet Immunol Immunopathol. 2010 Mar 15;134(1-2):33-8. doi: 10.1016/j.vetimm.2009.10.006. Epub 2009 Oct 14.

Abstract

Programmed death (PD) molecules belong to the B7 family of co-stimulatory proteins and function in adaptive immunity. PD-1 (CD279) is expressed on lymphocytes and macrophages, and its ligand (PD-L1, CD274) on immune cells and non-hematopoietic cells. Ligation of PD-1 on lymphocytes inhibits T-cell proliferation, cytokine production, and cytolytic function by phosphorylation of immunoreceptor tyrosine-based switch motifs and blockade of T cell receptor signaling. PD-1 and PD-L1 interactions are essential to maintain peripheral immune tolerance and to modulate activation of naïve T cells. Decreased expression results in autoimmunity in mouse models, and increased expression is a key feature of chronic viral infections in humans.

Publication types

  • Review

MeSH terms

  • Adaptive Immunity / physiology
  • Animals
  • Apoptosis / physiology
  • Apoptosis Regulatory Proteins / physiology*
  • Apoptosis Regulatory Proteins / ultrastructure
  • Humans
  • Lymphocytes / physiology
  • Lymphocytes / virology
  • Macrophages / physiology
  • Macrophages / virology
  • Mice
  • Signal Transduction / physiology
  • T-Lymphocytes / physiology
  • T-Lymphocytes / virology
  • Virus Diseases / immunology
  • Virus Diseases / virology

Substances

  • Apoptosis Regulatory Proteins