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A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection

Coronaviruses have caused several human epidemics and pandemics including the ongoing coronavirus disease 2019 (COVID-19). Prophylactic vaccines and therapeutic antibodies have already shown striking effectiveness against COVID-19. Nevertheless, concerns remain about antigenic drift in SARS-CoV-2 as...

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Autores principales: Liu, Hejun, Yuan, Meng, Huang, Deli, Bangaru, Sandhya, Zhao, Fangzhu, Lee, Chang-Chun D., Peng, Linghang, Barman, Shawn, Zhu, Xueyong, Nemazee, David, Burton, Dennis R., van Gils, Marit J., Sanders, Rogier W., Kornau, Hans-Christian, Reincke, S. Momsen, Prüss, Harald, Kreye, Jakob, Wu, Nicholas C., Ward, Andrew B., Wilson, Ian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049401/
https://www.ncbi.nlm.nih.gov/pubmed/33894127
http://dx.doi.org/10.1016/j.chom.2021.04.005
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author Liu, Hejun
Yuan, Meng
Huang, Deli
Bangaru, Sandhya
Zhao, Fangzhu
Lee, Chang-Chun D.
Peng, Linghang
Barman, Shawn
Zhu, Xueyong
Nemazee, David
Burton, Dennis R.
van Gils, Marit J.
Sanders, Rogier W.
Kornau, Hans-Christian
Reincke, S. Momsen
Prüss, Harald
Kreye, Jakob
Wu, Nicholas C.
Ward, Andrew B.
Wilson, Ian A.
author_facet Liu, Hejun
Yuan, Meng
Huang, Deli
Bangaru, Sandhya
Zhao, Fangzhu
Lee, Chang-Chun D.
Peng, Linghang
Barman, Shawn
Zhu, Xueyong
Nemazee, David
Burton, Dennis R.
van Gils, Marit J.
Sanders, Rogier W.
Kornau, Hans-Christian
Reincke, S. Momsen
Prüss, Harald
Kreye, Jakob
Wu, Nicholas C.
Ward, Andrew B.
Wilson, Ian A.
author_sort Liu, Hejun
collection PubMed
description Coronaviruses have caused several human epidemics and pandemics including the ongoing coronavirus disease 2019 (COVID-19). Prophylactic vaccines and therapeutic antibodies have already shown striking effectiveness against COVID-19. Nevertheless, concerns remain about antigenic drift in SARS-CoV-2 as well as threats from other sarbecoviruses. Cross-neutralizing antibodies to SARS-related viruses provide opportunities to address such concerns. Here, we report on crystal structures of a cross-neutralizing antibody, CV38-142, in complex with the receptor-binding domains from SARS-CoV-2 and SARS-CoV. Recognition of the N343 glycosylation site and water-mediated interactions facilitate cross-reactivity of CV38-142 to SARS-related viruses, allowing the antibody to accommodate antigenic variation in these viruses. CV38-142 synergizes with other cross-neutralizing antibodies, notably COVA1-16, to enhance neutralization of SARS-CoV and SARS-CoV-2, including circulating variants of concern B.1.1.7 and B.1.351. Overall, this study provides valuable information for vaccine and therapeutic design to address current and future antigenic drift in SARS-CoV-2 and to protect against zoonotic SARS-related coronaviruses.
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spelling pubmed-80494012021-04-16 A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection Liu, Hejun Yuan, Meng Huang, Deli Bangaru, Sandhya Zhao, Fangzhu Lee, Chang-Chun D. Peng, Linghang Barman, Shawn Zhu, Xueyong Nemazee, David Burton, Dennis R. van Gils, Marit J. Sanders, Rogier W. Kornau, Hans-Christian Reincke, S. Momsen Prüss, Harald Kreye, Jakob Wu, Nicholas C. Ward, Andrew B. Wilson, Ian A. Cell Host Microbe Article Coronaviruses have caused several human epidemics and pandemics including the ongoing coronavirus disease 2019 (COVID-19). Prophylactic vaccines and therapeutic antibodies have already shown striking effectiveness against COVID-19. Nevertheless, concerns remain about antigenic drift in SARS-CoV-2 as well as threats from other sarbecoviruses. Cross-neutralizing antibodies to SARS-related viruses provide opportunities to address such concerns. Here, we report on crystal structures of a cross-neutralizing antibody, CV38-142, in complex with the receptor-binding domains from SARS-CoV-2 and SARS-CoV. Recognition of the N343 glycosylation site and water-mediated interactions facilitate cross-reactivity of CV38-142 to SARS-related viruses, allowing the antibody to accommodate antigenic variation in these viruses. CV38-142 synergizes with other cross-neutralizing antibodies, notably COVA1-16, to enhance neutralization of SARS-CoV and SARS-CoV-2, including circulating variants of concern B.1.1.7 and B.1.351. Overall, this study provides valuable information for vaccine and therapeutic design to address current and future antigenic drift in SARS-CoV-2 and to protect against zoonotic SARS-related coronaviruses. Cell Press 2021-05-12 /pmc/articles/PMC8049401/ /pubmed/33894127 http://dx.doi.org/10.1016/j.chom.2021.04.005 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Hejun
Yuan, Meng
Huang, Deli
Bangaru, Sandhya
Zhao, Fangzhu
Lee, Chang-Chun D.
Peng, Linghang
Barman, Shawn
Zhu, Xueyong
Nemazee, David
Burton, Dennis R.
van Gils, Marit J.
Sanders, Rogier W.
Kornau, Hans-Christian
Reincke, S. Momsen
Prüss, Harald
Kreye, Jakob
Wu, Nicholas C.
Ward, Andrew B.
Wilson, Ian A.
A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection
title A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection
title_full A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection
title_fullStr A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection
title_full_unstemmed A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection
title_short A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection
title_sort combination of cross-neutralizing antibodies synergizes to prevent sars-cov-2 and sars-cov pseudovirus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049401/
https://www.ncbi.nlm.nih.gov/pubmed/33894127
http://dx.doi.org/10.1016/j.chom.2021.04.005
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