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针对 SARS-CoV-2 刺突蛋白多个表位的强效中和抗体。

Potent neutralizing antibodies against multiple epitopes on SARS-CoV-2 spike.

机构信息

Aaron Diamond AIDS Research Center, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, USA.

Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY, USA.

出版信息

Nature. 2020 Aug;584(7821):450-456. doi: 10.1038/s41586-020-2571-7. Epub 2020 Jul 22.

Abstract

The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic continues, with devasting consequences for 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 coronavirus. Here we report the isolation of sixty-one SARS-CoV-2-neutralizing monoclonal antibodies from five patients infected with SARS-CoV-2 and admitted to hospital with severe coronavirus disease 2019 (COVID-19). Among these are nineteen antibodies that potently neutralized authentic SARS-CoV-2 in vitro, nine of which exhibited very high potency, with 50% virus-inhibitory concentrations of 0.7 to 9 ng ml. Epitope mapping showed that this collection of nineteen antibodies was about equally divided between those directed against the receptor-binding domain (RBD) and those directed against 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 overlap with the domains at the top of the spike. Cryo-electron microscopy reconstructions of one antibody that targets the RBD, a second that targets the NTD, and a third that bridges two separate RBDs showed that the antibodies recognize 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.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)大流行仍在继续,给人类生命和全球经济带来了毁灭性的后果。发现和开发针对这种冠状病毒的病毒中和单克隆抗体可能是一种治疗或预防感染的方法。在这里,我们报告了从五名感染 SARS-CoV-2 并因严重 2019 年冠状病毒病(COVID-19)住院的患者中分离出的 61 种 SARS-CoV-2 中和单克隆抗体。其中有 19 种抗体在体外能有效中和真实的 SARS-CoV-2,其中 9 种具有非常高的效力,半数病毒抑制浓度为 0.7 至 9ng/ml。表位作图表明,这 19 种抗体的集合大致平均分为针对受体结合域(RBD)的抗体和针对 N 端结构域(NTD)的抗体,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区域重叠的四元表位。针对 RBD 的一种抗体、针对 NTD 的另一种抗体和桥接两个单独 RBD 的第三种抗体的冷冻电子显微镜重建表明,这些抗体识别刺突的封闭、“全部 RBD 向下”构象。其中一些单克隆抗体是作为针对 SARS-CoV-2 的潜在治疗和/或预防性药物进行临床开发的有希望的候选药物。

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