Association of T cell proliferative responses and phenotype with virus control in chronic progressive HIV-1 disease

J Infect Dis. 2004 Feb 1;189(3):515-9. doi: 10.1086/381038. Epub 2004 Jan 16.

Abstract

The role of T cell immunity in virus control during chronic infection was examined in 79 human immunodeficiency virus type 1 (HIV-1)-infected subjects randomized to receive antiretroviral therapy. HIV-1 p24-specific responses were detected in 20% of the subjects at baseline, increasing to 28% of the subjects at weeks 16-24. Induction of virologic suppression was associated with lower plasma HIV-1 RNA levels and a higher percentage of Fas+ CD8+ T cells at baseline, whereas maintenance of suppression was associated with higher CD4+ T cell counts and, marginally, with a higher percentage of Fas+ CD4+ T cells at weeks 16-24. These findings indicate that Fas coexpression on T cells, in addition to plasma HIV-1 RNA levels and CD4+ T cell counts, may predict virologic outcome.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anti-HIV Agents / therapeutic use
  • Biomarkers / blood
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / microbiology
  • Chronic Disease
  • Drug Therapy, Combination
  • Female
  • HIV Infections / blood
  • HIV Infections / drug therapy*
  • HIV Infections / virology
  • HIV Protease Inhibitors / therapeutic use
  • HIV-1* / isolation & purification
  • Humans
  • Lymphocyte Count
  • Male
  • Phenotype
  • Prospective Studies
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / microbiology*
  • Viral Load
  • fas Receptor / analysis

Substances

  • Anti-HIV Agents
  • Biomarkers
  • HIV Protease Inhibitors
  • fas Receptor