Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Departments of Medicine and Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Viruses. 2024 Jun 25;16(7):1014. doi: 10.3390/v16071014.
We recently demonstrated that Simian-HIV (SHIV)-infected neonate rhesus macaques (RMs) generated heterologous HIV-1 neutralizing antibodies (NAbs) with broadly-NAb (bNAb) characteristics at a higher frequency compared with their corresponding dam. Here, we characterized genetic diversity in Env sequences from four neonate or adult/dam RM pairs: in two pairs, neonate and dam RMs made heterologous HIV-1 NAbs; in one pair, neither the neonate nor the dam made heterologous HIV-1 NAbs; and in another pair, only the neonate made heterologous HIV-1 NAbs. Phylogenetic and sequence diversity analyses of longitudinal Envs revealed that a higher genetic diversity, within the host and away from the infecting SHIV strain, was correlated with heterologous HIV-1 NAb development. We identified 22 Env variable sites, of which 9 were associated with heterologous HIV-1 NAb development; 3/9 sites had mutations previously linked to HIV-1 Env bNAb development. These data suggested that viral diversity drives heterologous HIV-1 NAb development, and the faster accumulation of viral diversity in neonate RMs may be a potential mechanism underlying bNAb induction in pediatric populations. Moreover, these data may inform candidate Env immunogens to guide precursor B cells to bNAb status via vaccination by the Env-based selection of bNAb lineage members with the appropriate mutations associated with neutralization breadth.
我们最近证明,与相应的母猴相比,感染了猴免疫缺陷病毒(SHIV)的新生恒河猴(RMs)产生具有广泛中和抗体(bNAb)特征的异源 HIV-1 中和抗体(NAb)的频率更高。在这里,我们对来自四对新生或成年/母猴 RM 的 Env 序列进行了遗传多样性特征分析:在两对中,新生和母猴 RM 产生了异源 HIV-1 NAb;在一对中,新生和母猴均未产生异源 HIV-1 NAb;而在另一对中,只有新生猴产生了异源 HIV-1 NAb。对纵向 Env 的系统发育和序列多样性分析表明,宿主内和远离感染性 SHIV 株的更高遗传多样性与异源 HIV-1 NAb 发育相关。我们鉴定了 22 个 Env 可变位点,其中 9 个与异源 HIV-1 NAb 发育相关;3/9 个位点的突变与 HIV-1 Env bNAb 发育有关。这些数据表明病毒多样性驱动了异源 HIV-1 NAb 的产生,新生 RMs 中病毒多样性的快速积累可能是儿科人群中 bNAb 诱导的潜在机制。此外,这些数据可以为候选Env 免疫原提供信息,通过基于Env 的选择,使具有适当中和广度相关突变的 bNAb 谱系成员优先被疫苗选择,从而引导前体 B 细胞达到 bNAb 状态。