HIV-1 expression in chimpanzees can be activated by CD8+ cell depletion or CMV infection

Clin Immunol Immunopathol. 1992 Dec;65(3):227-33. doi: 10.1016/0090-1229(92)90151-d.

Abstract

CD8+ cell antiviral activity and cytomegalovirus (CMV) were investigated in vivo as possible cofactors influencing the outcome of HIV-1 infection. The role of CD8+ cell suppression of HIV replication was evaluated by depleting CD8+ cells in two infected chimpanzees by inoculation with monoclonal anti-CD8 antibodies. Two other infected animals were injected with chimpanzee CMV (CCMV)-infected human fibroblasts to determine if exposure to this virus would induce HIV replication. Treatment with anti-CD8 antibody resulted in recovery of virus from the CD4+ lymphocytes of one animal at 1, 4, and 6 months, and from a second animal at 1 month postinoculation. In contrast, virus had been recovered only once or not at all from these infected chimpanzees for 4 years prior to treatment. Similarly, HIV was recovered from the CD4+ cells of the two animals 2 to 3 months after inoculation of CCMV-infected fibroblasts but not after inoculation of control uninfected fibroblasts. These studies suggest that CD8+ cell-mediated suppression and the presence of other viruses (such as CMV) could act as cofactors in influencing the extent of HIV-1 replication in vivo and, possibly, progression to disease.

Publication types

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

MeSH terms

  • Animals
  • Antibody Formation
  • CD8 Antigens / immunology
  • Cytomegalovirus Infections / complications*
  • Cytomegalovirus Infections / immunology
  • HIV Antibodies / immunology
  • HIV Infections / complications
  • HIV Infections / immunology*
  • HIV-1 / growth & development*
  • HIV-1 / immunology
  • Lymphocyte Depletion
  • Pan troglodytes
  • T-Lymphocyte Subsets / immunology*
  • Virus Replication

Substances

  • CD8 Antigens
  • HIV Antibodies