Department of Chemistry and Biochemistry, Swarthmore College, Swarthmore, PA 19081, USA.
Viruses. 2021 Sep 5;13(9):1774. doi: 10.3390/v13091774.
Antibodies that can neutralize diverse HIV-1 strains develop in ~10-20% of HIV-1 infected individuals, and their elicitation is a goal of vaccine design. Such antibodies can also serve as therapeutics for those who have already been infected with the virus. Structural characterizations of broadly reactive antibodies in complex with the HIV-1 spike indicate that there are a limited number of sites of vulnerability on the spike. Analysis of their structures can help reveal commonalities that would be useful in vaccine design and provide insights on combinations of antibodies that can be used to minimize the incidence of viral resistance mutations. In this review, we give an update on recent structures determined of the spike in complex with broadly neutralizing antibodies in the context of all epitopes on the HIV-1 spike identified to date.
能够中和多种 HIV-1 毒株的抗体约在 10-20%的 HIV-1 感染者中产生,其诱导是疫苗设计的目标。此类抗体也可作为已感染病毒的治疗方法。与 HIV-1 刺突蛋白复合物中广泛反应性抗体的结构特征表明,刺突蛋白上存在数量有限的脆弱位点。对其结构的分析可以帮助揭示疫苗设计中有用的共性,并提供有关可用于最大程度减少病毒耐药性突变发生率的抗体组合的见解。在这篇综述中,我们根据迄今为止确定的 HIV-1 刺突蛋白上的所有表位,更新了最近与广泛中和抗体结合的刺突蛋白的结构。