首页> 外文期刊>Vaccine >Lessons from IAVI-006, a Phase I clinical trial to evaluate the safety and immunogenicity of the pTHr.HIVA DNA and MVA.HIVA vaccines in a prime-boost strategy to induce HIV-1 specific T-cell responses in healthy volunteers
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Lessons from IAVI-006, a Phase I clinical trial to evaluate the safety and immunogenicity of the pTHr.HIVA DNA and MVA.HIVA vaccines in a prime-boost strategy to induce HIV-1 specific T-cell responses in healthy volunteers

机译:IAVI-006的经验教训,I期临床试验旨在评估pTHr.HIVA DNA和MVA.HIVA疫苗在健康志愿者中诱导HIV-1特异性T细胞应答的初免-加强策略的安全性和免疫原性

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IAVI-006 was the first large randomised, double-blinded, placebo-controlled Phase I clinical trial to systematically investigate the prime-boost strategy for induction of HIV-1 specific CD8+ cytotoxic T-lymphocytes (CTL) in a factorial trial design using (i) priming with 0.5 mg or 2 mg of pTHr.HIVA DNA vaccine, followed by (ii) two booster vaccinations with 5 x 10(7) MVA.HIVA at weeks 8 and 12 (early boost) or weeks 20 and 24 (late boost). This Study set the basis for later clinical trials and dernonstrated the safety of these candidate HIV vaccines. The safety and immunogenicity results are presented and the lessons derived from this clinical trial are discussed. (C) 2008 Published by Elsevier Ltd.
机译:IAVI-006是第一个大型随机,双盲,安慰剂对照的I期临床试验,旨在通过因子分解试验设计,系统地研究诱导HIV-1特异性CD8 +细胞毒性T淋巴细胞(CTL)的初免-加强策略,使用( i)用0.5 mg或2 mg pTHr.HIVA DNA疫苗进行初次接种,然后(ii)在第8和12周(早期加强)或第20和24周(晚期)用5 x 10(7)MVA.HIVA加强免疫促进)。这项研究为以后的临床试验奠定了基础,并确定了这些候选HIV疫苗的安全性。介绍了安全性和免疫原性结果,并讨论了从该临床试验中得出的经验教训。 (C)2008由Elsevier Ltd.发布

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