HIV vaccine development.

David I Watkins
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Abstract

Updates on the Thai clinical vaccine trial, the discovery of additional neutralizing antibodies, and several new, nonhuman primate vaccine studies were presented at the 17th Conference on Retroviruses and Opportunistic Infections this year. Interestingly, the vaccine effect observed in the Thai trial diminished with time and was most effective in individuals who reported low-risk behavior. Two new neutralizing monoclonal antibodies were reported that were more potent and broadly reactive than the previously described monoclonal antibodies, giving the neutralization field an important boost. New studies were presented in macaques showing that a DNA prime modified vaccinia virus Ankara boost regimen can reduce acquisition of infection after a low-dose mucosal challenge with a heterologous pathogenic simian immunodeficiency virus (SIV) strain. Data suggesting that attenuated SIV vaccines can induce cellular immune responses that control viral replication were also discussed. Finally, and perhaps most encouragingly, vaccination with cytomegalovirus-expressing SIV antigens provided robust levels of protection against the highly pathogenic SIVmac239 viral isolate. All of these promising results should serve to energize the HIV vaccine field.

艾滋病毒疫苗开发。
在今年举行的第17届逆转录病毒和机会性感染会议上,介绍了泰国临床疫苗试验的最新情况、额外中和抗体的发现以及几项新的非人灵长类动物疫苗研究。有趣的是,在泰国试验中观察到的疫苗效果随着时间的推移而减弱,并且在报告低风险行为的个体中最有效。报道了两种新的中和单克隆抗体,它们比以前描述的单克隆抗体更有效,反应性更广,给中和领域带来了重要的推动。在猕猴中提出的新研究表明,DNA引物修饰的牛痘病毒安卡拉增强方案可以减少异源致病性猴免疫缺陷病毒(SIV)株低剂量粘膜攻击后的感染获得。还讨论了表明减毒SIV疫苗可以诱导控制病毒复制的细胞免疫反应的数据。最后,或许也是最令人鼓舞的是,接种表达巨细胞病毒SIV抗原的疫苗,对高致病性SIVmac239病毒分离物提供了强有力的保护。所有这些有希望的结果都将为艾滋病毒疫苗领域注入活力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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