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乙型流感血凝素第214位的单个突变增强了交叉中和作用。

A single mutation at position 214 of influenza B hemagglutinin enhances cross-neutralization.

作者信息

Cheng Ziqi, Sun Yeqing, Shen Yanru, Wu Xi, Pan Ling, Wu Hao, Bai Yunbo, Zhao Chenyan, Ma Junfeng, Huang Weijin

机构信息

National Engineering Laboratory for AIDS Vaccines, School of Life Sciences, Jilin University, Changchun, People's Republic of China.

Division of HIV/AIDS and Sexually transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC) and WHO Collaborating Center for Standardization and Evaluation of Biologicals, Beijing, People's Republic of China.

出版信息

Emerg Microbes Infect. 2025 Dec;14(1):2467770. doi: 10.1080/22221751.2025.2467770. Epub 2025 Feb 21.

Abstract

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.

摘要

乙型流感病毒(IBV)血凝素(HA)的高度变异性损害了疫苗的交叉中和能力,导致效力降低。我们发现IBV毒株B/怀俄明/06/2014和B/布里斯班/60/2008之间在交叉中和方面存在显著差异,这两种毒株仅在三个氨基酸残基上有所不同。发现214T点突变可显著增强交叉中和作用(>10倍)。基于抗体的反向验证还表明,该突变显著提高了中和能力(500 - 62500倍)。此外,监测显示该位点的突变率已达到近20年来的最高水平,在某些地区提交的序列中流行率超过80%。我们的研究结果为选择具有改善交叉中和效果的疫苗毒株提供了新证据,这将有助于通过修饰最小抗原表位来开发广谱疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/538b/11849025/b0e79f8c433e/TEMI_A_2467770_F0001_OC.jpg

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