病毒学
概念证明
计算生物学
生物
计算机科学
操作系统
作者
Michelle C. Crank,Tracy J. Ruckwardt,Man Chen,Kaitlyn M. Morabito,Emily Phung,Pamela Costner,LaSonji A. Holman,Somia P. Hickman,Nina M. Berkowitz,Ingelise J. Gordon,Galina V. Yamshchikov,Martin R. Gaudinski,Azad Kumar,Lauren A. Chang,Syed M. Moin,Juliane P. Hill,Anthony DiPiazza,Richard Schwartz,Lisa A. Kueltzo,Jonathan W. Cooper
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2019-08-01
卷期号:365 (6452): 505-509
被引量:272
标识
DOI:10.1126/science.aav9033
摘要
Building a better RSV vaccine Respiratory syncytial virus (RSV) causes severe respiratory disease, especially in infants and the elderly. However, attempts to produce effective human vaccines have largely been unsuccessful. Structure-based design has been used to generate an RSV fusion glycoprotein stabilized in its prefusion conformation (DS-Cav1). This immunogen is highly effective in mice and macaques. Crank et al. now report the results of a phase I vaccine clinical trial using the stabilized prefusion DS-Cav1 molecule. Four weeks after immunization, these vaccines elicited substantially more high-quality antibody titers than those typically generated using earlier RSV immunogens. The findings provide a proof of concept for how structural biology can contribute to precision vaccine design. Science , this issue p. 505
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