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Novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating SARS-CoV-2 variants and sarbecoviruses

The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants of concern, including Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2), and Omicron (B.1.1.529) has aroused concerns over their increased infectivity and transmissibility, as well as decreased sensi...

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Autores principales: Wang, Yingdan, Liu, Meiqin, Shen, Yaping, Ma, Yunping, Li, Xiang, Zhang, Yuanyuan, Liu, Mei, Yang, Xing-Lou, Chen, Jun, Yan, Renhong, Luan, Die, Wang, Yanqun, Chen, Ying, Wang, Qimin, Lin, Haofeng, Li, Yaning, Wu, Kaiyue, Zhu, Tongyu, Zhao, Jincun, Lu, Hongzhou, Wen, Yumei, Jiang, Shibo, Wu, Fan, Zhou, Qiang, Shi, Zheng-Li, Huang, Jinghe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021188/
https://www.ncbi.nlm.nih.gov/pubmed/35443747
http://dx.doi.org/10.1038/s41421-022-00401-6
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author Wang, Yingdan
Liu, Meiqin
Shen, Yaping
Ma, Yunping
Li, Xiang
Zhang, Yuanyuan
Liu, Mei
Yang, Xing-Lou
Chen, Jun
Yan, Renhong
Luan, Die
Wang, Yanqun
Chen, Ying
Wang, Qimin
Lin, Haofeng
Li, Yaning
Wu, Kaiyue
Zhu, Tongyu
Zhao, Jincun
Lu, Hongzhou
Wen, Yumei
Jiang, Shibo
Wu, Fan
Zhou, Qiang
Shi, Zheng-Li
Huang, Jinghe
author_facet Wang, Yingdan
Liu, Meiqin
Shen, Yaping
Ma, Yunping
Li, Xiang
Zhang, Yuanyuan
Liu, Mei
Yang, Xing-Lou
Chen, Jun
Yan, Renhong
Luan, Die
Wang, Yanqun
Chen, Ying
Wang, Qimin
Lin, Haofeng
Li, Yaning
Wu, Kaiyue
Zhu, Tongyu
Zhao, Jincun
Lu, Hongzhou
Wen, Yumei
Jiang, Shibo
Wu, Fan
Zhou, Qiang
Shi, Zheng-Li
Huang, Jinghe
author_sort Wang, Yingdan
collection PubMed
description The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants of concern, including Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2), and Omicron (B.1.1.529) has aroused concerns over their increased infectivity and transmissibility, as well as decreased sensitivity to SARS-CoV-2-neutralizing antibodies (NAbs) and the current coronavirus disease 2019 (COVID-19) vaccines. Such exigencies call for the development of pan-sarbecovirus vaccines or inhibitors to combat the circulating SARS-CoV-2 NAb-escape variants and other sarbecoviruses. In this study, we isolated a broadly NAb against sarbecoviruses named GW01 from a donor who recovered from COVID-19. Cryo-EM structure and competition assay revealed that GW01 targets a highly conserved epitope in a wide spectrum of different sarbecoviruses. However, we found that GW01, the well-known sarbecovirus NAb S309, and the potent SARS-CoV-2 NAbs CC12.1 and REGN10989 only neutralize about 90% of the 56 tested currently circulating variants of SARS-CoV-2 including Omicron. Therefore, to improve efficacy, we engineered an IgG-like bispecific antibody GW01-REGN10989 (G9) consisting of single-chain antibody fragments (scFv) of GW01 and REGN10989. We found that G9 could neutralize 100% of NAb-escape mutants (23 out of 23), including Omicron variant, with a geometric mean (GM) 50% inhibitory concentration of 8.8 ng/mL. G9 showed prophylactic and therapeutic effects against SARS-CoV-2 infection of both the lung and brain in hACE2-transgenic mice. Site-directed mutagenesis analyses revealed that GW01 and REGN10989 bind to the receptor-binding domain in different epitopes and from different directions. Since G9 targets the epitopes for both GW01 and REGN10989, it was effective against variants with resistance to GW01 or REGN10989 alone and other NAb-escape variants. Therefore, this novel bispecific antibody, G9, is a strong candidate for the treatment and prevention of infection by SARS-CoV-2, NAb-escape variants, and other sarbecoviruses that may cause future emerging or re-emerging coronavirus diseases.
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spelling pubmed-90211882022-04-28 Novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating SARS-CoV-2 variants and sarbecoviruses Wang, Yingdan Liu, Meiqin Shen, Yaping Ma, Yunping Li, Xiang Zhang, Yuanyuan Liu, Mei Yang, Xing-Lou Chen, Jun Yan, Renhong Luan, Die Wang, Yanqun Chen, Ying Wang, Qimin Lin, Haofeng Li, Yaning Wu, Kaiyue Zhu, Tongyu Zhao, Jincun Lu, Hongzhou Wen, Yumei Jiang, Shibo Wu, Fan Zhou, Qiang Shi, Zheng-Li Huang, Jinghe Cell Discov Article The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants of concern, including Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2), and Omicron (B.1.1.529) has aroused concerns over their increased infectivity and transmissibility, as well as decreased sensitivity to SARS-CoV-2-neutralizing antibodies (NAbs) and the current coronavirus disease 2019 (COVID-19) vaccines. Such exigencies call for the development of pan-sarbecovirus vaccines or inhibitors to combat the circulating SARS-CoV-2 NAb-escape variants and other sarbecoviruses. In this study, we isolated a broadly NAb against sarbecoviruses named GW01 from a donor who recovered from COVID-19. Cryo-EM structure and competition assay revealed that GW01 targets a highly conserved epitope in a wide spectrum of different sarbecoviruses. However, we found that GW01, the well-known sarbecovirus NAb S309, and the potent SARS-CoV-2 NAbs CC12.1 and REGN10989 only neutralize about 90% of the 56 tested currently circulating variants of SARS-CoV-2 including Omicron. Therefore, to improve efficacy, we engineered an IgG-like bispecific antibody GW01-REGN10989 (G9) consisting of single-chain antibody fragments (scFv) of GW01 and REGN10989. We found that G9 could neutralize 100% of NAb-escape mutants (23 out of 23), including Omicron variant, with a geometric mean (GM) 50% inhibitory concentration of 8.8 ng/mL. G9 showed prophylactic and therapeutic effects against SARS-CoV-2 infection of both the lung and brain in hACE2-transgenic mice. Site-directed mutagenesis analyses revealed that GW01 and REGN10989 bind to the receptor-binding domain in different epitopes and from different directions. Since G9 targets the epitopes for both GW01 and REGN10989, it was effective against variants with resistance to GW01 or REGN10989 alone and other NAb-escape variants. Therefore, this novel bispecific antibody, G9, is a strong candidate for the treatment and prevention of infection by SARS-CoV-2, NAb-escape variants, and other sarbecoviruses that may cause future emerging or re-emerging coronavirus diseases. Springer Nature Singapore 2022-04-21 /pmc/articles/PMC9021188/ /pubmed/35443747 http://dx.doi.org/10.1038/s41421-022-00401-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Yingdan
Liu, Meiqin
Shen, Yaping
Ma, Yunping
Li, Xiang
Zhang, Yuanyuan
Liu, Mei
Yang, Xing-Lou
Chen, Jun
Yan, Renhong
Luan, Die
Wang, Yanqun
Chen, Ying
Wang, Qimin
Lin, Haofeng
Li, Yaning
Wu, Kaiyue
Zhu, Tongyu
Zhao, Jincun
Lu, Hongzhou
Wen, Yumei
Jiang, Shibo
Wu, Fan
Zhou, Qiang
Shi, Zheng-Li
Huang, Jinghe
Novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating SARS-CoV-2 variants and sarbecoviruses
title Novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating SARS-CoV-2 variants and sarbecoviruses
title_full Novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating SARS-CoV-2 variants and sarbecoviruses
title_fullStr Novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating SARS-CoV-2 variants and sarbecoviruses
title_full_unstemmed Novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating SARS-CoV-2 variants and sarbecoviruses
title_short Novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating SARS-CoV-2 variants and sarbecoviruses
title_sort novel sarbecovirus bispecific neutralizing antibodies with exceptional breadth and potency against currently circulating sars-cov-2 variants and sarbecoviruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021188/
https://www.ncbi.nlm.nih.gov/pubmed/35443747
http://dx.doi.org/10.1038/s41421-022-00401-6
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