HIV-1 DNA/MVA vaccination reduces the per exposure probability of infection during repeated mucosal SHIV challenges

被引:38
作者
Ellenberger, Dennis
Otten, Ronald A.
Li, Bin
Aidoo, Michael
Rodriguez, I. Vanessa
Sariol, Carlos A.
Martinez, Melween
Monsour, Michael
Wyatt, Linda
Hudgens, Michael G.
Edmundo, Kraiselburd
Bernard, Moss
Robinson, Harriet
Thomas, Folks
Butera, Salvatore
机构
[1] Ctr Dis Control & Prevent, Lab Branch, Div HIV AIDS Prevent, Natl Ctr HIV STD & TB Prevent, Atlanta, GA 30333 USA
[2] Ctr Dis Control & Prevent, Stat & Data Management Branch, Div HIV AIDS Prevent, Natl Ctr HIV STD & TB Prevent, Atlanta, GA 30333 USA
[3] Caribbean Primate Res Ctr, Unit Comparat Med, San Juan, PR 00936 USA
[4] Caribbean Primate Res Ctr, Dept Microbiol & Med Zool, San Juan, PR 00936 USA
[5] NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
[6] Univ N Carolina, Dept Biostat, Sch Publ Hlth, Chapel Hill, NC 27599 USA
[7] Emory Univ, Yerkes Reg Primate Res Ctr, Atlanta, GA 30322 USA
关键词
repetitive virus challenge; mucosal challenge; vaccine; DNA/MVA; non-human primate model; human sexual transmission; SHIV;
D O I
10.1016/j.virol.2006.04.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Historically, HIV vaccines specifically designed to raise cellular immunity resulted in protection from disease progression but not infection when tested in monkeys challenged with a single high virus exposure. An alternative approach, more analogous to human sexual exposures, is to repetitively challenge immunized monkeys with a much lower dose of virus until systemic infection is documented. Using these conditions to mimic human sexual transmission, we found that a multi-protein DNA/MVA HIV-1 vaccine is indeed capable of protecting rhesus monkeys against systemic infection when repeatedly challenged with a highly heterologous immunodeficiency virus (SHIV). Furthermore, this repetitive challenge approach allowed us to calculate per-exposure probability of infection, an observed vaccine efficacy of 64%, and undertake a systematic analysis for correlates of protection based on exposures needed to achieve infection. Therefore, improved non-human primate models for vaccine efficacy can provide novel insight and perhaps renew expectations for positive outcomes of human HIV clinical trials. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:216 / 225
页数:10
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