Liu Lihong, Wang Pengfei, Nair Manoj S, Yu Jian, Rapp Micah, Wang Qian, Luo Yang, Chan Jasper F-W, Sahi Vincent, Figueroa Amir, Guo Xinzheng V, Cerutti Gabriele, Bimela Jude, Gorman Jason, Zhou Tongqing, Chen Zhiwei, Yuen Kwok-Yung, Kwong Peter D, Sodroski Joseph G, Yin Michael T, Sheng Zizhang, Huang Yaoxing, Shapiro Lawrence, Ho David D
bioRxiv. 2020 Jul 16:2020.06.17.153486. doi: 10.1101/2020.06.17.153486.
The SARS-CoV-2 pandemic rages on with devasting consequences on human lives and the global economy . The discovery and development of virus-neutralizing monoclonal antibodies could be one approach to treat or prevent infection by this novel coronavirus. Here we report the isolation of 61 SARS-CoV-2-neutralizing monoclonal antibodies from 5 infected patients hospitalized with severe disease. Among these are 19 antibodies that potently neutralized the authentic SARS-CoV-2 , 9 of which exhibited exquisite potency, with 50% virus-inhibitory concentrations of 0.7 to 9 ng/mL. Epitope mapping showed this collection of 19 antibodies to be about equally divided between those directed to the receptor-binding domain (RBD) and those to the N-terminal domain (NTD), indicating that both of these regions at the top of the viral spike are immunogenic. In addition, two other powerful neutralizing antibodies recognized quaternary epitopes that are overlapping with the domains at the top of the spike. Cryo-electron microscopy reconstructions of one antibody targeting RBD, a second targeting NTD, and a third bridging two separate RBDs revealed recognition of the closed, "all RBD-down" conformation of the spike. Several of these monoclonal antibodies are promising candidates for clinical development as potential therapeutic and/or prophylactic agents against SARS-CoV-2.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)大流行仍在肆虐,对人类生命和全球经济造成了毁灭性后果。发现和开发病毒中和单克隆抗体可能是治疗或预防这种新型冠状病毒感染的一种方法。在此,我们报告了从5名因重症住院的感染患者中分离出61种SARS-CoV-2中和单克隆抗体。其中有19种抗体能有效中和野生型SARS-CoV-2,其中9种表现出极高的效力,50%病毒抑制浓度为0.7至9 ng/mL。表位作图显示,这19种抗体大致平均分为靶向受体结合域(RBD)的抗体和靶向N端结构域(NTD)的抗体,这表明病毒刺突顶端的这两个区域都具有免疫原性。此外,另外两种强大的中和抗体识别与刺突顶端结构域重叠的四级表位。对一种靶向RBD的抗体、第二种靶向NTD的抗体以及第三种桥接两个独立RBD的抗体进行冷冻电子显微镜重建,揭示了对刺突的封闭“所有RBD向下”构象的识别。这些单克隆抗体中的几种有望作为抗SARS-CoV-2的潜在治疗和/或预防药物进行临床开发。