Multivalent Epigraph Hemagglutinin Vaccine Protects against Influenza B Virus in Mice

被引:2
|
作者
Petro-Turnquist, Erika [1 ]
Kampfe, Brigette Corder [1 ,2 ]
Gadeken, Amber [3 ]
Pekarek, Matthew J. [1 ]
Weaver, Eric A. [1 ]
机构
[1] Univ Nebraska, Nebraska Ctr Virol, Sch Biol Sci, Lincoln, NE 68583 USA
[2] North Arkansas Coll, Sci Dept, Harrison, AR 72601 USA
[3] Univ Nebraska, Coll Agr Sci & Nat Resources, Lincoln, NE 68583 USA
来源
PATHOGENS | 2024年 / 13卷 / 02期
基金
美国国家卫生研究院;
关键词
influenza B virus; yamagata lineage; victoria lineage; epigraph; vaccine; UNITED-STATES; IMMUNITY; INFECTION; SEASON;
D O I
10.3390/pathogens13020097
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Influenza B virus is a respiratory pathogen that contributes to seasonal epidemics, accounts for approximately 25% of global influenza infections, and can induce severe disease in young children. While vaccination is the most commonly used method of preventing influenza infections, current vaccines only induce strain-specific responses and have suboptimal efficacy when mismatched from circulating strains. Further, two influenza B virus lineages have been described, B/Yamagata-like and B/Victoria-like, and the limited cross-reactivity between the two lineages provides an additional barrier in developing a universal influenza B virus vaccine. Here, we report a novel multivalent vaccine using computationally designed Epigraph hemagglutinin proteins targeting both the B/Yamagata-like and B/Victoria-like lineages. When compared to the quadrivalent commercial vaccine, the Epigraph vaccine demonstrated increased breadth of neutralizing antibody and T cell responses. After lethal heterologous influenza B virus challenge, mice immunized with the Epigraph vaccine were completely protected against both weight loss and mortality. The superior cross-reactive immunity conferred by the Epigraph vaccine immunogens supports their continued investigation as a universal influenza B virus vaccine.
引用
收藏
页数:17
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