| Literature DB >> 33893388 |
Deyong Song1, Wenbo Wang2, Chuangchuang Dong1, Zhenfei Ning1, Xiu Liu1, Chuan Liu3, Guangying Du4, Chunjie Sha4, Kailin Wang1, Jun Lu1, Baiping Sun1, Yanyan Zhao1, Qiaoping Wang1, Hongguang Xu1, Ying Li1, Zhenduo Shen1, Jie Jiao1, Ruiying Wang4, Jingwei Tian4, Wanhui Liu4, Lan Wang5, Yong-Qiang Deng6, Changlin Dou7.
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the ongoing COVID-19 pandemic, which has resulted in more than two million deaths at 2021 February . There is currently no approved therapeutics for treating COVID-19. The SARS-CoV-2 Spike protein is considered a key therapeutic target by many researchers. Here we describe the identification of several monoclonal antibodies that target SARS-CoV-2 Spike protein. One human antibody, CA521FALA, demonstrated neutralization potential by immunizing human antibody transgenic mice. CA521FALA showed potent SARS-CoV-2-specific neutralization activity against SARS-CoV-2 pseudovirus and authentic SARS-CoV-2 infection in vitro. CA521FALA also demonstrated having a long half-life of 9.5 days in mice and 9.3 days in rhesus monkeys. CA521FALA inhibited SARS-CoV-2 infection in SARS-CoV-2 susceptible mice at a therapeutic setting with virus titer of the lung reduced by 4.5 logs. Structural analysis by cryo-EM revealed that CA521FALA recognizes an epitope overlapping with angiotensin converting enzyme 2 (ACE2)-binding sites in SARS-CoV-2 RBD in the Spike protein. CA521FALA blocks the interaction by binding all three RBDs of one SARS-CoV-2 spike trimer simultaneously. These results demonstrate the importance for antibody-based therapeutic interventions against COVID-19 and identifies CA521FALA a promising antibody that reacts with SARS-CoV-2 Spike protein to strongly neutralize its activity.Entities:
Year: 2021 PMID: 33893388 DOI: 10.1038/s42003-021-02029-w
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642