Long-term protection of chimpanzees against high-dose HIV-1 challenge induced by immunization

A combination AIDS vaccine approach consisting of priming with adenovirus-HIV-1 MN gp160 recom-binants followed by boosting with HIV-1 SF2 gp120 was evaluated in chimpanzees. Long-lasting protection, requiring only three immunizations, was achieved against a low-dose challenge with the SF2 strain of...

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Veröffentlicht in:Nature medicine 1997-06, Vol.3 (6), p.651-658
Hauptverfasser: Lubeck, Michael D., Natuk, Robert, Myagkikh, Maria, Kalyan, Narender, Aldrich, Kristine, Sinangil, Faruk, Alipanah, Shabnam, Murthy, Shri C.S., Chanda, Pranab K., Nigida, Stephen M., Markham, Phillip D., Zolla-pazner, Susan, Steimer, Kathy, Wade, Mark, Reitz, Marvin S., Arthur, Larry O., Mizutani, Satoshi, Davis, Alan, Hung, Paul P., Gallo, Robert C., Eichberg, Jorg, Robert-Guroff, Marjorie
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Sprache:eng
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Zusammenfassung:A combination AIDS vaccine approach consisting of priming with adenovirus-HIV-1 MN gp160 recom-binants followed by boosting with HIV-1 SF2 gp120 was evaluated in chimpanzees. Long-lasting protection, requiring only three immunizations, was achieved against a low-dose challenge with the SF2 strain of HIV-1 and a subsequent high-dose SF2 challenge administered 1 year later without an intervening boost. Notably, neutralizing antibody responses against both clinical and laboratory isolates developed in three chimpanzees and persisted until the time of high-dose challenge. The possibility that cytotoxic T-lymphocytes contribute to low-dose protection of a chimpanzee lacking neutralizing antibodies is suggested. Our results validate the live vector priming/subunit booster approach and should stimulate interest in assessing this combination vaccine approach in humans.
ISSN:1078-8956
1546-170X
DOI:10.1038/nm0697-651