Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037, USA.
Cell Host Microbe. 2012 Oct 18;12(4):396-407. doi: 10.1016/j.chom.2012.09.008.
Despite numerous attempts over many years to develop an HIV vaccine based on classical strategies, none has convincingly succeeded to date. A number of approaches are being pursued in the field, including building upon possible efficacy indicated by the recent RV144 clinical trial, which combined two HIV vaccines. Here, we argue for an approach based, in part, on understanding the HIV envelope spike and its interaction with broadly neutralizing antibodies (bnAbs) at the molecular level and using this understanding to design immunogens as possible vaccines. BnAbs can protect against virus challenge in animal models, and many such antibodies have been isolated recently. We further propose that studies focused on how best to provide T cell help to B cells that produce bnAbs are crucial for optimal immunization strategies. The synthesis of rational immunogen design and immunization strategies, together with iterative improvements, offers great promise for advancing toward an HIV vaccine.
尽管多年来人们尝试了许多基于经典策略的 HIV 疫苗研发方法,但迄今为止没有一种方法令人信服地成功。目前正在该领域探索多种方法,包括利用最近 RV144 临床试验的可能疗效,该试验结合了两种 HIV 疫苗。在这里,我们主张采用一种方法,部分基于对 HIV 包膜刺突及其与广泛中和抗体(bnAbs)在分子水平上相互作用的理解,并利用这种理解来设计免疫原作为可能的疫苗。bnAbs 可以在动物模型中预防病毒攻击,最近已经分离出许多这样的抗体。我们进一步提出,专注于如何最好地为产生 bnAbs 的 B 细胞提供 T 细胞帮助的研究对于最佳免疫策略至关重要。理性免疫原设计和免疫策略的综合,以及迭代改进,为推进 HIV 疫苗的研发提供了巨大的希望。