U.S. Military HIV Research Program, Center of Infectious Disease Research, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA; Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
Vaccine Research Center, NIAID, NIH, Bethesda, MD 20892, USA.
Cell Host Microbe. 2021 Apr 14;29(4):564-578.e9. doi: 10.1016/j.chom.2021.01.016. Epub 2021 Mar 3.
Determining which immunological mechanisms contribute to the development of broad neutralizing antibodies (bNAbs) during HIV-1 infection is a major goal to inform vaccine design. Using samples from a longitudinal HIV-1 acute infection cohort, we found key B cell determinants within the first 14-43 days of viremia that predict the development of bNAbs years later. Individuals who develop neutralization breadth had significantly higher B cell engagement with the autologous founder HIV envelope (Env) within 1 month of initial viremia. A higher frequency of founder-Env-specific naive B cells was associated with increased B cell activation and differentiation and predictive of bNAb development. These data demonstrate that the initial B cell interaction with the founder HIV Env is important for the development of broadly neutralizing antibodies and provide evidence that events within HIV acute infection lead to downstream functional outcomes.
确定哪些免疫机制有助于 HIV-1 感染期间产生广谱中和抗体(bNAbs)是为疫苗设计提供信息的主要目标。使用来自 HIV-1 急性感染纵向队列的样本,我们在病毒血症的最初 14-43 天内发现了关键的 B 细胞决定因素,这些因素可预测数年后 bNAbs 的发展。在初始病毒血症后 1 个月内,具有中和广度的个体与自身的 HIV 包膜(Env)的原始 B 细胞有明显更高的结合。与原始 Env 特异性幼稚 B 细胞的高频率相关的是 B 细胞激活和分化的增加,并预测 bNAb 的发展。这些数据表明,初始 B 细胞与原始 HIV Env 的相互作用对于产生广谱中和抗体很重要,并提供了证据表明 HIV 急性感染中的事件导致下游功能结果。