Antigen-driven C-C chemokine-mediated HIV-1 suppression by CD4(+) T cells from exposed uninfected individuals expressing the wild-type CCR-5 allele

J Exp Med. 1997 Aug 4;186(3):455-60. doi: 10.1084/jem.186.3.455.

Abstract

Despite repeated exposure to HIV-1, certain individuals remain persistently uninfected. Such exposed uninfected (EU) people show evidence of HIV-1-specific T cell immunity and, in rare cases, selective resistance to infection by macrophage-tropic strains of HIV-1. The latter has been associated with a 32-base pair deletion in the C-C chemokine receptor gene CCR-5, the major coreceptor of macrophage-tropic strains of HIV-1. We have undertaken an analysis of the HIV-specific T cell responses in 12 EU individuals who were either homozygous for the wild-type CCR-5 allele or heterozygous for the deletion allele (CCR-5Delta32). We have found evidence of an oligoclonal T cell response mediated by helper T cells specific for a conserved region of the HIV-1 envelope. These cells produce very high levels of C-C chemokines when stimulated by the specific antigen and suppress selectively the replication of macrophage-tropic, but not T cell-tropic, strains of HIV-1. These chemokine-producing helper cells may be part of a protective immune response that could be potentially exploited for vaccine development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Amino Acid Sequence
  • Anti-HIV Agents / immunology*
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / virology*
  • Chemokines / biosynthesis
  • Chemokines / physiology*
  • Clone Cells
  • Genotype
  • HIV Envelope Protein gp120 / immunology*
  • HIV Envelope Protein gp120 / physiology*
  • HIV-1 / genetics
  • HIV-1 / physiology*
  • Humans
  • Lymphocyte Activation / genetics
  • Molecular Sequence Data
  • Peptides / chemical synthesis
  • Peptides / immunology
  • Receptors, CCR5
  • Receptors, Cytokine / genetics*
  • Receptors, HIV / genetics*
  • Virus Replication / immunology

Substances

  • Anti-HIV Agents
  • Chemokines
  • HIV Envelope Protein gp120
  • Peptides
  • Receptors, CCR5
  • Receptors, Cytokine
  • Receptors, HIV