中和
病毒学
病毒
呼吸系统
接种疫苗
生物
抗原
佐剂
免疫学
解剖
作者
Lionel Sacconnay,Jonathan De Smedt,Vera Rocha‐Perugini,Edison Ong,Romuald Mascolo,Anne Atas,Carline Vanden Abeele,Magali de Heusch,Nathalie De Schrevel,Marie‐Pierre David,Badiaa Bouzya,Kim Stobbelaar,Yannick Vanloubbeeck,Peter Delputte,Corey P. Mallett,Nancy Dezutter,Lucile Warter
出处
期刊:Science Translational Medicine
[American Association for the Advancement of Science (AAAS)]
日期:2023-08-23
卷期号:15 (710)
被引量:9
标识
DOI:10.1126/scitranslmed.adg6050
摘要
The RSVPreF3-AS01 vaccine, containing the respiratory syncytial virus (RSV) prefusion F protein and the AS01 adjuvant, was previously shown to boost neutralization responses against historical RSV strains and to be efficacious in preventing RSV-associated lower respiratory tract diseases in older adults. Although RSV F is highly conserved, variation does exist between strains. Here, we characterized variations in the major viral antigenic sites among contemporary RSV sequences when compared with RSVPreF3 and showed that, in older adults, RSVPreF3-AS01 broadly boosts neutralization responses against currently dominant and antigenically distant RSV strains. RSV-neutralizing responses are thought to play a central role in preventing RSV infection. Therefore, the breadth of RSVPreF3-AS01–elicited neutralization responses may contribute to vaccine efficacy against contemporary RSV strains and those that may emerge in the future.
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