Cytotoxic T-lymphocyte responses to cytomegalovirus in normal and simian immunodeficiency virus-infected rhesus macaques

A Kaur, MD Daniel, D Hempel, D Lee-Parritz… - Journal of …, 1996 - Am Soc Microbiol
A Kaur, MD Daniel, D Hempel, D Lee-Parritz, MS Hirsch, RP Johnson
Journal of virology, 1996Am Soc Microbiol
Disseminated cytomegalovirus (CMV) infection is a frequent occurrence in human
immunodeficiency virus-infected humans and in simian immunodeficiency virus (SIV)-
infected rhesus macaques. Rhesus macaques are a suitable animal model with which to
study in vivo interactions between CMV and AIDS-associated retroviruses. Since cytotoxic T
lymphocytes (CTL) play a major role in control of viral infections, we have characterized
CMV-specific CTL responses in SIV-infected and uninfected rhesus macaques. Autologous …
Disseminated cytomegalovirus (CMV) infection is a frequent occurrence in human immunodeficiency virus-infected humans and in simian immunodeficiency virus (SIV)-infected rhesus macaques. Rhesus macaques are a suitable animal model with which to study in vivo interactions between CMV and AIDS-associated retroviruses. Since cytotoxic T lymphocytes (CTL) play a major role in control of viral infections, we have characterized CMV-specific CTL responses in SIV-infected and uninfected rhesus macaques. Autologous fibroblasts infected with rhesus CMV were used to stimulate freshly isolated peripheral blood mononuclear cells from CMV-seropositive animals. Following in vitro stimulation, specific CTL activity against CMV-infected autologous fibroblasts was detected in CMV-seropositive but not in CMV-seronegative normal macaques. CMV-specific CTL activity comparable to that in normal animals was also detected in two CMV-seropositive macaques infected with a live attenuated SIV strain (SIVdelta3) and in two of three macaques infected with pathogenic SIV strains. The CMV-specific CTL response was class I major histocompatibility complex restricted and mediated by CD8+ cells. An early CMV protein(s) was the dominant target recognized by bulk CTL, although the pattern of CTL recognition of CMV proteins varied among animals. Analysis of CMV-specific CTL responses in macaques should serve as a valuable model for CMV immunopathogenesis and will facilitate prospective in vivo studies of immune interactions between CMV and SIV in AIDS.
American Society for Microbiology