Vigorous HIV-1-specific CD4+ T cell responses associated with control of viremia

Science. 1997 Nov 21;278(5342):1447-50. doi: 10.1126/science.278.5342.1447.

Abstract

Virus-specific CD4+ T helper lymphocytes are critical to the maintenance of effective immunity in a number of chronic viral infections, but are characteristically undetectable in chronic human immunodeficiency virus-type 1 (HIV-1) infection. In individuals who control viremia in the absence of antiviral therapy, polyclonal, persistent, and vigorous HIV-1-specific CD4+ T cell proliferative responses were present, resulting in the elaboration of interferon-gamma and antiviral beta chemokines. In persons with chronic infection, HIV-1-specific proliferative responses to p24 were inversely related to viral load. Strong HIV-1-specific proliferative responses were also detected following treatment of acutely infected persons with potent antiviral therapy. The HIV-1-specific helper cells are likely to be important in immunotherapeutic interventions and vaccine development.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Anti-HIV Agents / therapeutic use
  • Chemokines / biosynthesis
  • Cohort Studies
  • Cytotoxicity, Immunologic
  • Disease Progression
  • Drug Therapy, Combination
  • HIV Core Protein p24 / immunology
  • HIV Envelope Protein gp160 / immunology
  • HIV Infections / drug therapy
  • HIV Infections / immunology*
  • HIV Infections / virology*
  • HIV-1 / immunology*
  • HIV-1 / physiology
  • Humans
  • Immunologic Memory
  • Interferon-gamma / biosynthesis
  • Lymphocyte Activation
  • Molecular Sequence Data
  • Peptide Fragments / immunology
  • T-Lymphocytes, Cytotoxic / immunology
  • T-Lymphocytes, Helper-Inducer / immunology*
  • Viral Load
  • Viremia / immunology*
  • Viremia / virology
  • Virus Replication

Substances

  • Anti-HIV Agents
  • Chemokines
  • HIV Core Protein p24
  • HIV Envelope Protein gp160
  • Peptide Fragments
  • Interferon-gamma