Lewis George K, Pazgier Marzena, DeVico Anthony L
Division of Vaccine Research, Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
Immunol Rev. 2017 Jan;275(1):271-284. doi: 10.1111/imr.12510.
It is clear that antibodies can play a pivotal role in preventing the transmission of HIV-1 and large efforts to identify an effective antibody-based vaccine to quell the epidemic. Shortly after HIV-1 was discovered as the cause of AIDS, the search for epitopes recognized by neutralizing antibodies became the driving strategy for an antibody-based vaccine. Neutralization escape variants were discovered shortly thereafter, and, after almost three decades of investigation, it is now known that autologous neutralizing antibody responses and their selection of neutralization resistant HIV-1 variants can lead to broadly neutralizing antibodies in some infected individuals. This observation drives an intensive effort to identify a vaccine to elicit broadly neutralizing antibodies. In contrast, there has been less systematic study of antibody specificities that must rely mainly or exclusively on other protective mechanisms, although non-human primate (NHP) studies as well as the RV144 vaccine trial indicate that non-neutralizing antibodies can contribute to protection. Here we propose a novel strategy to identify new epitope targets recognized by these antibodies for which viral escape is unlikely or impossible.
显然,抗体在预防HIV-1传播方面可发挥关键作用,人们也付出了巨大努力来寻找一种有效的基于抗体的疫苗以遏制这一流行病。在HIV-1被发现是艾滋病病因后不久,寻找被中和抗体识别的表位就成为基于抗体疫苗的主导策略。此后不久就发现了中和逃逸变体,经过近三十年的研究,现在已知自体中和抗体反应及其对中和抗性HIV-1变体的选择可在一些受感染个体中产生广泛中和抗体。这一观察结果促使人们大力努力寻找一种能引发广泛中和抗体的疫苗。相比之下,对于主要或完全依赖其他保护机制的抗体特异性,系统性研究较少,尽管非人灵长类动物(NHP)研究以及RV144疫苗试验表明非中和抗体可有助于提供保护。在此,我们提出一种新策略,以识别这些抗体识别的新表位靶点,而针对这些靶点病毒不太可能或不可能发生逃逸。