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一种具有两种作用机制的广谱抗乙型流感病毒治疗性抗体。

A broadly protective therapeutic antibody against influenza B virus with two mechanisms of action.

机构信息

Department of Infectious Diseases, Genentech, South San Francisco, California 94080, USA.

Department of Translational Immunology, Genentech, South San Francisco, California 94080, USA.

出版信息

Nat Commun. 2017 Jan 19;8:14234. doi: 10.1038/ncomms14234.

Abstract

Influenza B virus (IBV) causes annual influenza epidemics around the world. Here we use an in vivo plasmablast enrichment technique to isolate a human monoclonal antibody, 46B8 that neutralizes all IBVs tested in vitro and protects mice against lethal challenge of all IBVs tested when administered 72 h post infection. 46B8 demonstrates a superior therapeutic benefit over Tamiflu and has an additive antiviral effect in combination with Tamiflu. 46B8 binds to a conserved epitope in the vestigial esterase domain of hemagglutinin (HA) and blocks HA-mediated membrane fusion. After passage of the B/Brisbane/60/2008 virus in the presence of 46B8, we isolated three resistant clones, all harbouring the same mutation (Ser301Phe) in HA that abolishes 46B8 binding to HA at low pH. Interestingly, 46B8 is still able to protect mice against lethal challenge of the mutant viruses, possibly owing to its ability to mediate antibody-dependent cellular cytotoxicity (ADCC).

摘要

乙型流感病毒(IBV)在全球范围内引起季节性流感流行。在这里,我们使用体内浆母细胞富集技术分离出一种人源单克隆抗体 46B8,该抗体能够中和体外所有测试的 IBV,并在感染后 72 小时给药时保护小鼠免受所有测试的 IBV 的致死性攻击。46B8 比 Tamiflu 具有更好的治疗效果,并且与 Tamiflu 联合使用具有抗病毒的附加作用。46B8 结合到血凝素(HA)残余酯酶结构域中的保守表位,阻止 HA 介导的膜融合。在存在 46B8 的情况下,使 B/Brisbane/60/2008 病毒传代后,我们分离出三个具有相同突变(Ser301Phe)的抗性克隆,该突变在低 pH 下使 46B8 与 HA 的结合完全丧失。有趣的是,46B8 仍然能够保护小鼠免受突变病毒的致死性攻击,这可能是由于其介导抗体依赖性细胞毒性(ADCC)的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/135f/5253702/2aa7bfb6268a/ncomms14234-f1.jpg

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