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Human-IgG-Neutralizing Monoclonal Antibodies Block the SARS-CoV-2 Infection

Coronavirus disease 2019 (COVID-19) has become a worldwide threat to humans, and neutralizing antibodies have therapeutic potential. We have purified more than 1,000 memory B cells specific to SARS-CoV-2 S1 or its RBD (receptor binding domain) and obtain 729 paired heavy- and light-chain fragments....

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Autores principales: Wan, Jinkai, Xing, Shenghui, Ding, Longfei, Wang, Yongheng, Gu, Chenjian, Wu, Yanling, Rong, Bowen, Li, Cheng, Wang, Siqing, Chen, Kun, He, Chenxi, Zhu, Dandan, Yuan, Songhua, Qiu, Chengli, Zhao, Chen, Nie, Lei, Gao, Zhangzhao, Jiao, Jingyu, Zhang, Xiaoyan, Wang, Xiangxi, Ying, Tianlei, Wang, Haibin, Xie, Youhua, Lu, Yanan, Xu, Jianqing, Lan, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332464/
https://www.ncbi.nlm.nih.gov/pubmed/32668215
http://dx.doi.org/10.1016/j.celrep.2020.107918
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author Wan, Jinkai
Xing, Shenghui
Ding, Longfei
Wang, Yongheng
Gu, Chenjian
Wu, Yanling
Rong, Bowen
Li, Cheng
Wang, Siqing
Chen, Kun
He, Chenxi
Zhu, Dandan
Yuan, Songhua
Qiu, Chengli
Zhao, Chen
Nie, Lei
Gao, Zhangzhao
Jiao, Jingyu
Zhang, Xiaoyan
Wang, Xiangxi
Ying, Tianlei
Wang, Haibin
Xie, Youhua
Lu, Yanan
Xu, Jianqing
Lan, Fei
author_facet Wan, Jinkai
Xing, Shenghui
Ding, Longfei
Wang, Yongheng
Gu, Chenjian
Wu, Yanling
Rong, Bowen
Li, Cheng
Wang, Siqing
Chen, Kun
He, Chenxi
Zhu, Dandan
Yuan, Songhua
Qiu, Chengli
Zhao, Chen
Nie, Lei
Gao, Zhangzhao
Jiao, Jingyu
Zhang, Xiaoyan
Wang, Xiangxi
Ying, Tianlei
Wang, Haibin
Xie, Youhua
Lu, Yanan
Xu, Jianqing
Lan, Fei
author_sort Wan, Jinkai
collection PubMed
description Coronavirus disease 2019 (COVID-19) has become a worldwide threat to humans, and neutralizing antibodies have therapeutic potential. We have purified more than 1,000 memory B cells specific to SARS-CoV-2 S1 or its RBD (receptor binding domain) and obtain 729 paired heavy- and light-chain fragments. Among these, 178 antibodies test positive for antigen binding, and the majority of the top 17 binders with EC(50) below 1 nM are RBD binders. Furthermore, we identify 11 neutralizing antibodies, eight of which show IC(50) within 10 nM, and the best one, 414-1, with IC(50) of 1.75 nM. Through epitope mapping, we find three main epitopes in RBD recognized by these antibodies, and epitope-B antibody 553-15 could substantially enhance the neutralizing abilities of most of the other antibodies. We also find that 515-5 could cross neutralize the SARS-CoV pseudovirus. Altogether, our study provides 11 potent human neutralizing antibodies for COVID-19 as therapeutic candidates.
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spelling pubmed-73324642020-07-06 Human-IgG-Neutralizing Monoclonal Antibodies Block the SARS-CoV-2 Infection Wan, Jinkai Xing, Shenghui Ding, Longfei Wang, Yongheng Gu, Chenjian Wu, Yanling Rong, Bowen Li, Cheng Wang, Siqing Chen, Kun He, Chenxi Zhu, Dandan Yuan, Songhua Qiu, Chengli Zhao, Chen Nie, Lei Gao, Zhangzhao Jiao, Jingyu Zhang, Xiaoyan Wang, Xiangxi Ying, Tianlei Wang, Haibin Xie, Youhua Lu, Yanan Xu, Jianqing Lan, Fei Cell Rep Article Coronavirus disease 2019 (COVID-19) has become a worldwide threat to humans, and neutralizing antibodies have therapeutic potential. We have purified more than 1,000 memory B cells specific to SARS-CoV-2 S1 or its RBD (receptor binding domain) and obtain 729 paired heavy- and light-chain fragments. Among these, 178 antibodies test positive for antigen binding, and the majority of the top 17 binders with EC(50) below 1 nM are RBD binders. Furthermore, we identify 11 neutralizing antibodies, eight of which show IC(50) within 10 nM, and the best one, 414-1, with IC(50) of 1.75 nM. Through epitope mapping, we find three main epitopes in RBD recognized by these antibodies, and epitope-B antibody 553-15 could substantially enhance the neutralizing abilities of most of the other antibodies. We also find that 515-5 could cross neutralize the SARS-CoV pseudovirus. Altogether, our study provides 11 potent human neutralizing antibodies for COVID-19 as therapeutic candidates. The Author(s). 2020-07-21 2020-07-03 /pmc/articles/PMC7332464/ /pubmed/32668215 http://dx.doi.org/10.1016/j.celrep.2020.107918 Text en © 2020 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Wan, Jinkai
Xing, Shenghui
Ding, Longfei
Wang, Yongheng
Gu, Chenjian
Wu, Yanling
Rong, Bowen
Li, Cheng
Wang, Siqing
Chen, Kun
He, Chenxi
Zhu, Dandan
Yuan, Songhua
Qiu, Chengli
Zhao, Chen
Nie, Lei
Gao, Zhangzhao
Jiao, Jingyu
Zhang, Xiaoyan
Wang, Xiangxi
Ying, Tianlei
Wang, Haibin
Xie, Youhua
Lu, Yanan
Xu, Jianqing
Lan, Fei
Human-IgG-Neutralizing Monoclonal Antibodies Block the SARS-CoV-2 Infection
title Human-IgG-Neutralizing Monoclonal Antibodies Block the SARS-CoV-2 Infection
title_full Human-IgG-Neutralizing Monoclonal Antibodies Block the SARS-CoV-2 Infection
title_fullStr Human-IgG-Neutralizing Monoclonal Antibodies Block the SARS-CoV-2 Infection
title_full_unstemmed Human-IgG-Neutralizing Monoclonal Antibodies Block the SARS-CoV-2 Infection
title_short Human-IgG-Neutralizing Monoclonal Antibodies Block the SARS-CoV-2 Infection
title_sort human-igg-neutralizing monoclonal antibodies block the sars-cov-2 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332464/
https://www.ncbi.nlm.nih.gov/pubmed/32668215
http://dx.doi.org/10.1016/j.celrep.2020.107918
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