Quadrivalent influenza nanoparticle vaccines induce broad protection

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作者
Seyhan Boyoglu-Barnum
Daniel Ellis
Rebecca A. Gillespie
Geoffrey B. Hutchinson
Young-Jun Park
Syed M. Moin
Oliver J. Acton
Rashmi Ravichandran
Mike Murphy
Deleah Pettie
Nick Matheson
Lauren Carter
Adrian Creanga
Michael J. Watson
Sally Kephart
Sila Ataca
John R. Vaile
George Ueda
Michelle C. Crank
Lance Stewart
Kelly K. Lee
Miklos Guttman
David Baker
John R. Mascola
David Veesler
Barney S. Graham
Neil P. King
Masaru Kanekiyo
机构
[1] National Institutes of Health,Vaccine Research Center, National Institute of Allergy and Infectious Diseases
[2] University of Washington,Institute for Protein Design
[3] University of Washington,Department of Biochemistry
[4] University of Washington,Graduate Program in Molecular and Cellular Biology
[5] University of Washington,Department of Medicinal Chemistry
[6] University of Washington,Howard Hughes Medical Institute
[7] The Francis Crick Institute,Macromolecular Structure Laboratory
来源
Nature | 2021年 / 592卷
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摘要
Influenza vaccines that confer broad and durable protection against diverse viral strains would have a major effect on global health, as they would lessen the need for annual vaccine reformulation and immunization1. Here we show that computationally designed, two-component nanoparticle immunogens2 induce potently neutralizing and broadly protective antibody responses against a wide variety of influenza viruses. The nanoparticle immunogens contain 20 haemagglutinin glycoprotein trimers in an ordered array, and their assembly in vitro enables the precisely controlled co-display of multiple distinct haemagglutinin proteins in defined ratios. Nanoparticle immunogens that co-display the four haemagglutinins of licensed quadrivalent influenza vaccines elicited antibody responses in several animal models against vaccine-matched strains that were equivalent to or better than commercial quadrivalent influenza vaccines, and simultaneously induced broadly protective antibody responses to heterologous viruses by targeting the subdominant yet conserved haemagglutinin stem. The combination of potent receptor-blocking and cross-reactive stem-directed antibodies induced by the nanoparticle immunogens makes them attractive candidates for a supraseasonal influenza vaccine candidate with the potential to replace conventional seasonal vaccines3.
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页码:623 / 628
页数:5
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