中和
病毒学
血凝素(流感)
点突变
表位
突变
生物
抗原漂移
抗原
病毒
抗体
免疫逃逸
遗传学
基因
免疫系统
作者
Ziqi Cheng,Yeqing Sun,Yanru Shen,Xi Wu,Ling Pan,Hao Wu,Yunbo Bai,Chenyan Zhao,Junfeng Ma,Weijin Huang
标识
DOI:10.1080/22221751.2025.2467770
摘要
High variability of influenza B virus (IBV) hemagglutinin (HA) impairs the cross- neutralization ability of vaccines, leading to reduce efficacy. We identified significant differences in cross-neutralization between IBV strains B/Wyoming/06/2014 and B/Brisbane/60/2008, which differ in only three amino acid residues. The 214 T point mutation was found to dramatically enhance cross-neutralization (>10-fold). Antibody-based reverse validation also revealed that this mutation significantly increased the neutralization capacity (500-62,500-fold). Furthermore, monitoring revealed that the mutation rate at this site has reached its highest level in nearly 20 years, with a prevalence exceeding 80% in sequences submitted from certain regions. Our findings provide new evidence for the selection of vaccine strains with improved cross- neutralization effects, which will aid the development of broad-spectrum vaccines by modifying minimal antigenic epitopes.
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