Addetia Amin, Perruzza Lisa, Park Young-Jun, McCallum Matthew, Stewart Cameron, Brown Jack T, Donati Alessia, Culap Katja, Balmelli Alessio, Gazi Michal, Carrion Ricardo, Corti Davide, Benigni Fabio, Veesler David
Department of Biochemistry, University of Washington, Seattle, WA, 9815, USA.
Humabs Biomed SA, a Subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.
bioRxiv. 2025 May 18:2025.05.14.654121. doi: 10.1101/2025.05.14.654121.
Marburg virus (MARV) is a filovirus that causes a severe and often lethal hemorrhagic fever. Despite the increasing frequency of MARV outbreaks, no vaccines or therapeutics are licensed for use in humans. Here, we designed mutations that improve the expression and thermostability of the prefusion MARV glycoprotein (GP) ectodomain trimer, which is the sole target of neutralizing antibodies and vaccines in development. We discovered a fully human monoclonal antibody, MARV16, that broadly neutralizes all MARV isolates as well as Ravn virus and Dehong virus with 40 to 100-fold increased potency relative to previously described antibodies. We determined a cryo-electron microscopy structure of MARV16-bound MARV GP showing that MARV16 recognizes a prefusion-specific epitope spanning GP1 and GP2, blocking receptor binding and preventing conformational changes required for viral entry. We further reveal the architecture of the MARV GP glycan cap, which shields the receptor binding site (RBS), underscoring architectural similarities with distantly related filovirus GPs. MARV16 and previously identified RBS-directed antibodies can bind MARV GP simultaneously, paving the way for a MARV therapeutic antibody cocktail. MARV GP stabilization along with the discovery of a potent neutralizing antibody will advance treatment and prevention options for MARV.
马尔堡病毒(MARV)是一种丝状病毒,可引起严重且往往致命的出血热。尽管马尔堡病毒疫情的发生频率不断增加,但目前尚无获批用于人类的疫苗或治疗方法。在此,我们设计了一些突变,以改善融合前马尔堡病毒糖蛋白(GP)胞外域三聚体的表达和热稳定性,该三聚体是正在研发的中和抗体和疫苗的唯一靶点。我们发现了一种完全人源单克隆抗体MARV16,它能广泛中和所有马尔堡病毒分离株以及拉文病毒和德宏病毒,相对于先前描述的抗体,其效力提高了40至100倍。我们确定了与MARV16结合的MARV GP的冷冻电子显微镜结构,结果表明MARV16识别一个跨越GP1和GP2的融合前特异性表位,阻断受体结合并防止病毒进入所需的构象变化。我们进一步揭示了马尔堡病毒GP聚糖帽的结构,该结构屏蔽了受体结合位点(RBS),突出了与远亲丝状病毒GP在结构上的相似性。MARV16和先前鉴定的RBS导向抗体可同时结合MARV GP,为马尔堡病毒治疗性抗体鸡尾酒疗法铺平了道路。马尔堡病毒GP的稳定以及一种强效中和抗体的发现将推动马尔堡病毒治疗和预防方案的发展。