病毒学
拉沙病毒
沙粒病毒
生物
病毒
埃博拉病毒
朱宁病毒
中和抗体
抗体
糖蛋白
先天免疫系统
免疫
免疫系统
免疫学
遗传学
CD8型
淋巴细胞性脉络膜脑膜炎
作者
Stéphanie Reynard,Xavier Carnec,Caroline Picard,Virginie Borges-Cardoso,Alexandra Journeaux,Mathieu Mateo,Clara Germain,Jimmy Hortion,Laure Albrecht,Émeline Perthame,Natalia Pietrosemoli,Audrey Vallvé,Stéphane Barron,Aurélie Duthey,Orianne Lacroix,Ophélie Jourjon,Marie Moroso,Lyne Fellmann,Pierre‐Henri Moreau,Maïlys Daniau
标识
DOI:10.1038/s41564-022-01281-y
摘要
Pathogenic New World arenaviruses (NWAs) cause haemorrhagic fevers and can have high mortality rates, as shown in outbreaks in South America. Neutralizing antibodies (Abs) are critical for protection from NWAs. Having shown that the MOPEVAC vaccine, based on a hyperattenuated arenavirus, induces neutralizing Abs against Lassa fever, we hypothesized that expression of NWA glycoproteins in this platform might protect against NWAs. Cynomolgus monkeys immunized with MOPEVACMAC, targeting Machupo virus, prevented the lethality of this virus and induced partially NWA cross-reactive neutralizing Abs. We then developed the pentavalent MOPEVACNEW vaccine, expressing glycoproteins from all pathogenic South American NWAs. Immunization of cynomolgus monkeys with MOPEVACNEW induced neutralizing Abs against five NWAs, strong innate followed by adaptive immune responses as detected by transcriptomics and provided sterile protection against Machupo virus and the genetically distant Guanarito virus. MOPEVACNEW may thus be efficient to protect against existing and potentially emerging NWAs.
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