病毒学
病毒
血凝素(流感)
生物
抗体
接种疫苗
抗原
H5N1基因结构
抗原漂移
流感疫苗
甲型流感病毒
大流行
抗原变异
原罪
核苷
免疫学
医学
2019年冠状病毒病(COVID-19)
传染病(医学专业)
疾病
遗传学
病理
作者
Claudia P. Arevalo,Marcus J. Bolton,Valerie Le Sage,Naiqing Ye,Colleen Furey,Hiromi Muramatsu,Mohamad‐Gabriel Alameh,Norbert Pardi,Elizabeth M. Drapeau,Kaela Parkhouse,Tyler A. Garretson,Jeffrey S. Morris,Louise H. Moncla,Ying K. Tam,Steven H.Y. Fan,Seema S. Lakdawala,Drew Weissman,Scott E. Hensley
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-11-24
卷期号:378 (6622): 899-904
被引量:169
标识
DOI:10.1126/science.abm0271
摘要
Seasonal influenza vaccines offer little protection against pandemic influenza virus strains. It is difficult to create effective prepandemic vaccines because it is uncertain which influenza virus subtype will cause the next pandemic. In this work, we developed a nucleoside-modified messenger RNA (mRNA)–lipid nanoparticle vaccine encoding hemagglutinin antigens from all 20 known influenza A virus subtypes and influenza B virus lineages. This multivalent vaccine elicited high levels of cross-reactive and subtype-specific antibodies in mice and ferrets that reacted to all 20 encoded antigens. Vaccination protected mice and ferrets challenged with matched and mismatched viral strains, and this protection was at least partially dependent on antibodies. Our studies indicate that mRNA vaccines can provide protection against antigenically variable viruses by simultaneously inducing antibodies against multiple antigens.
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