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Analysis of intercurrent human immunodeficiency virus type 1 infections in phase I and II trials of candidate AIDS vaccines. AIDS Vaccine Evaluation Group, and the Correlates of HIV Immune Protection Group.

作者信息

Graham B S, McElrath M J, Connor R I, Schwartz D H, Gorse G J, Keefer M C, Mulligan M J, Matthews T J, Wolinsky S M, Montefiori D C, Vermund S H, Lambert J S, Corey L, Belshe R B, Dolin R, Wright P F, Korber B T, Wolff M C, Fast P E

机构信息

Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2582, USA.

出版信息

J Infect Dis. 1998 Feb;177(2):310-9. doi: 10.1086/514209.

Abstract

Among 2099 uninfected subjects in phase I and II trials of candidate AIDS vaccines, 23 were diagnosed with intercurrent human immunodeficiency virus type 1 (HIV-1) infection. High-risk sexual exposures accounted for 17 infections, and intravenous drug use accounted for 6. Four subjects received placebo, 13 received a complete immunization schedule (> or = 3 injections), and 6 were partially immunized (< or = 2 injections). There was no significant difference between vaccine recipients and control groups in incidence of HIV-1 infection, virus load, CD4 lymphocyte count, or V3 loop amino acid sequence. In summary, 19 vaccinated subjects acquired HIV-1 infection during phase I and II trials, indicating that immunization with the products described is < 100% effective in preventing or rapidly clearing infection. Laboratory analysis suggested that vaccine-induced immune responses did not significantly affect the genotypic or phenotypic characteristics of transmitted virus or the early clinical course of HIV-1 infection.

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