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恒河猴感染猴免疫缺陷病毒的幼仔与成年母猴成对个体的病毒包膜进化。

Viral Envelope Evolution in Simian-HIV-Infected Neonate and Adult-Dam Pairs of Rhesus Macaques.

机构信息

Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.

Departments of Medicine and Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Viruses. 2024 Jun 25;16(7):1014. doi: 10.3390/v16071014.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ab7/11281369/9f620d17cc8f/viruses-16-01014-g001.jpg

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