J Gen Virol
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J Gen Virol 73 (1992), 2273-2281; DOI 10.1099/0022-1317-73-9-2273
© 1992 Society for General Microbiology

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Potential significance of the cellular immune response against the macaque strain of simian immunodeficiency virus (SIVMAC) in immunized and infected rhesus macaques

Gerald Voss, Sigrid Nick, Christiane Stahl-Hennig, Cheick Coulibaly, Harald Petry, Wolfgang Lüke and Gerhard Hunsmann

Deutsches Primatenzentrum, Abteilung für Virologie und Immunologie, Kellnerweg 4, W-3400 Göttingen, Germany

The cellular immune response of seven rhesus macaques immunized with Tween-ether-treated macaque strain of simian immunodeficiency virus (SIVMAC) and three non-vaccinated control animals was investigated. Immunization elicited antigen-specific proliferating CD4+ cells in five of seven monkeys. Proliferating T cells were found in all animals protected from a first virus challenge. Cytotoxic T lymphocytes (CTLs) were not induced by the immunization. After the second challenge, the four formerly protected animals became infected, despite a strong proliferative CD4+ cell activity in three of them. All animals lost their proliferative activity 2 weeks after infection. After the first challenge four of the six infected animals exhibited a CTL response and after the second challenge, one of four newly infected macaques acquired a CTL response. The five animals with a CTL activity against SIVMAC proteins were protected from severe thrombo-cytopenia, which appeared in the five CTL-negative animals after infection. Our data show the induction of proliferative T cells by immunization with soluble SIVMAC antigen. This T cell reactivity was found in all animals protected from the first virus challenge, but did not confer protection from the second challenge. Interestingly, the proliferative T cell reactivity disappeared 2 weeks after virus infection. Furthermore a CTL response against viral proteins seems to protect infected animals from severe thrombocytopenia which is an early sign of AIDS in monkeys.

Received 13 January 1992; accepted 12 May 1992.





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Copyright © 1992 by the Society for General Microbiology.