National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University, Changchun 130012, China.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Int J Mol Sci. 2023 Aug 10;24(16):12642. doi: 10.3390/ijms241612642.
HIV-1 vaccines have been challenging to develop, partly due to the high level of genetic variation in its genome. Thus, a vaccine that can induce cross-reactive neutralization activities will be needed. Studies on the co-evolution of antibodies and viruses indicate that mimicking the natural infection is likely to induce broadly neutralizing antibodies (bnAbs). We generated the consensus Env sequence for each time point in subject CH505, who developed broad neutralization activities, and selected five critical time points before broad neutralization was detected. These consensus sequences were designed to express stable Env trimers. Priming with the transmitted/founder Env timer and sequential boosting with these consensus Env trimers from different time points induced broader and more potent neutralizing activities than the BG505 Env trimer in guinea pigs. Analysis of the neutralization profiles showed that sequential immunization of Env trimers favored nAbs with gp120/gp41 interface specificity while the BG505 Env trimer favored nAbs with V2 specificity. The unique features such as consensus sequences, stable Env trimers and the sequential immunization to mimic natural infection likely has allowed the induction of improved neutralization responses.
HIV-1 疫苗的研发一直具有挑战性,部分原因是其基因组具有高度的遗传变异性。因此,需要能够诱导交叉反应性中和活性的疫苗。抗体和病毒的共同进化研究表明,模拟自然感染可能会诱导广泛中和抗体(bnAbs)。我们针对产生广泛中和活性的受试者 CH505 的每个时间点生成了 Consensus Env 序列,并选择了在检测到广泛中和之前的五个关键时间点。这些 Consensus 序列被设计为表达稳定的 Env 三聚体。用传播/原始 Env 三聚体进行初始免疫,然后用来自不同时间点的这些 Consensus Env 三聚体进行连续加强免疫,在豚鼠中诱导出比 BG505 Env 三聚体更广泛和更强的中和活性。中和谱分析表明,Env 三聚体的连续免疫有利于具有 gp120/gp41 界面特异性的 nAbs,而 BG505 Env 三聚体则有利于具有 V2 特异性的 nAbs。Consensus 序列、稳定的 Env 三聚体和模拟自然感染的连续免疫等独特特征可能允许诱导出改进的中和反应。