T cell apoptosis in human immunodeficiency virus type 2- and simian immunodeficiency virus-infected macaques

J Gen Virol. 1996 Oct:77 ( Pt 10):2433-6. doi: 10.1099/0022-1317-77-10-2433.

Abstract

Recent evidence suggests that T cell apoptosis could be involved in the pathogenesis of HIV infection. In addition, lymphocyte apoptosis has been described in SIV-infected macaques that developed simian AIDS. To investigate further the role of apoptosis in AIDS pathogenesis, we studied lymphocytes of HIV-2-infected cynomolgus macaques that did not develop simian AIDS. We compared apoptosis of lymphocytes from animals infected with non-pathogenic HIV-2 to that in macaques infected with pathogenic SIV. Unfractionated peripheral blood mononuclear cells of SIV- and HIV-2-infected macaques showed evidence of apoptosis by electron microscopy, flow cytometry (terminal dUTP nick end labelling) and visualization of DNA fragmentation. Between 30-50% apoptotic cells could be detected in SIV-infected animals, compared to approximately 30% in HIV-2-infected and 5-12% in uninfected monkeys. However, separation of PBMC into T cell subpopulations revealed striking differences in apoptosis between SIV- and HIV-2-infected macaques. In SIV-infected monkeys both CD4 and CD8 cells underwent apoptosis to a large extent. In contrast, in the HIV-2-infected macaques apoptosis was restricted to the CD8 cell compartment. The lack of apoptosis in CD4 cells of healthy HIV-2-infected macaques implies an important role for CD4 cell apoptosis in AIDS pathogenesis.

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • CD4-Positive T-Lymphocytes / pathology*
  • CD8-Positive T-Lymphocytes / pathology*
  • DNA Fragmentation
  • Disease Models, Animal
  • Flow Cytometry
  • HIV Infections / physiopathology*
  • HIV-2 / pathogenicity*
  • Humans
  • Macaca fascicularis
  • Simian Acquired Immunodeficiency Syndrome / physiopathology*
  • Simian Immunodeficiency Virus / pathogenicity*