Avoiding the kiss of death: how HIV and other chronic viruses survive

Curr Opin Immunol. 2002 Aug;14(4):478-86. doi: 10.1016/s0952-7915(02)00366-7.

Abstract

Virus-specific CD8 T cells during chronic infection often exceed in numbers virus-replicating infected cells. Why then do antiviral CD8 T cells not do a better job of controlling infection? Although viral strategies for immune evasion are well known, this review will focus on changes in the CD8 T cell that interfere with cytolytic function. Most antiviral CD8 T cells in chronic infection do not express perforin, a molecule that is required for cytolysis. IL-2 and other costimulatory signals can restore cytotoxicity that has been impaired, suggesting a role for CD4 T cell anergy. The chance to eradicate an infection by T cell mediated lysis is undermined after an infection becomes established, in part because the effector immune response is impaired in the setting of chronic antigen.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Animals
  • Cell Differentiation
  • Chronic Disease
  • Clonal Anergy
  • Disease Models, Animal
  • HIV Infections / immunology*
  • Humans
  • Membrane Glycoproteins / physiology
  • Mice
  • Models, Immunological
  • Perforin
  • Pore Forming Cytotoxic Proteins
  • Simian Acquired Immunodeficiency Syndrome / immunology
  • T-Lymphocytes, Cytotoxic / immunology*
  • Virus Diseases / immunology*
  • Viruses / pathogenicity*

Substances

  • Membrane Glycoproteins
  • Pore Forming Cytotoxic Proteins
  • Perforin