病毒学
二价(发动机)
中和
单克隆抗体
病毒
帕利珠单抗
抗原
生物
免疫系统
多克隆抗体
接种疫苗
抗体
表位
免疫
抗原变异
中和抗体
副粘病毒科
原罪
单克隆
蛋白质亚单位
肺病毒科
免疫学
单反病毒
病菌
微生物学
突变体
体外
作者
Wei R. Chen,Lyndsey T. Martinez,Larissa Falcao,Zhenghui Li,Andrew McKeen,Chaitanya Kurhade,Hélène Boigard,Vidia Roopchand,Imani Richardson,Trisha Dasgupta,Katrina E. Llamera,Jing Colatat,Linda Goding Brock,Annaliesa S. Anderson,Kena A. Swanson
出处
期刊:npj vaccines
[Nature Portfolio]
日期:2026-03-14
卷期号:11 (1)
标识
DOI:10.1038/s41541-026-01418-8
摘要
Respiratory syncytial virus (RSV) is the leading global cause of serious respiratory disease in infants and an important respiratory pathogen in older adults. The RSV prefusion F protein (preF) is a major target of neutralizing antibodies shown to protect against RSV disease. The bivalent preF protein subunit vaccine (RSVpreF; Abrysvo®) contains stabilized preF antigens representing the two major RSV subgroups, RSV A and RSV B. Here, we characterized the neutralizing activity of adult RSVpreF immune sera against a panel of 65 contemporary, globally circulating RSV A and RSV B clinical isolates, containing various amino acid substitutions across the five major antigenic sites of RSV F (Ø, I, II, III, V). Monoclonal Ab-resistant mutant strains (MARMs) displaying in vitro resistance to nirsevimab, clesrovimab, and palivizumab (up to 300,000-fold resistance over the parental strain) were also evaluated. RSVpreF immune sera effectively neutralized both the panel of global clinical isolates and all MARMs tested. These findings demonstrate that the bivalent RSVpreF polyclonal response maintains robust neutralizing activity against circulating RSV A and B strains, including those that escape RSV F mAbs, and provides broad protective immunity against RSV.
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