Macrophage-dependent apoptosis of CD4+ T lymphocytes from HIV-infected individuals is mediated by FasL and tumor necrosis factor

J Exp Med. 1997 Jan 6;185(1):55-64. doi: 10.1084/jem.185.1.55.

Abstract

Apoptosis of bystander uninfected CD4+ T lymphocytes by neighboring HIV-infected cells is observed in cell culture and in lymphoid tissue of HIV-infected individuals. This study addresses whether antigen-presenting cells such as human macrophages mediate apoptosis of CD4+ T cells from HIV-infected individuals. Uninfected human macrophages, and to a larger degree, HIV-infected macrophages mediate apoptosis of T cells from HIV-infected, but not from uninfected control individuals. This macrophage-dependent killing targets CD4+, but not CD8+ T lymphocytes from HIV-infected individuals, and direct contact between macrophages and lymphocytes is required. Additional analyses indicated that the apoptosis-inducing ligands, FasL and tumor necrosis factor (TNF), mediate this macrophage-induced apoptosis of CD4+ T cells. These results support a role for macrophage-associated FasL and TNF in the selective depletion of CD4+ T cells in HIV-infected individuals.

MeSH terms

  • Antibodies, Monoclonal
  • Antigens, Surface / physiology
  • Apoptosis*
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / physiology
  • CD8-Positive T-Lymphocytes / immunology*
  • Cells, Cultured
  • Coculture Techniques
  • Fas Ligand Protein
  • Flow Cytometry
  • HIV Infections / immunology*
  • HIV Seronegativity
  • HIV Seropositivity / immunology
  • Humans
  • Lymphoid Tissue / immunology
  • Macrophages / immunology*
  • Membrane Glycoproteins / physiology*
  • Recombinant Fusion Proteins / immunology
  • Tumor Necrosis Factor-alpha / physiology*

Substances

  • Antibodies, Monoclonal
  • Antigens, Surface
  • FASLG protein, human
  • Fas Ligand Protein
  • Membrane Glycoproteins
  • Recombinant Fusion Proteins
  • Tumor Necrosis Factor-alpha