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Discovery and multimerization of cross-reactive single-domain antibodies against SARS-like viruses to enhance potency and address emerging SARS-CoV-2 variants

Coronaviruses have been the causative agent of three epidemics and pandemics in the past two decades, including the ongoing COVID-19 pandemic. A broadly-neutralizing coronavirus therapeutic is desirable not only to prevent and treat COVID-19, but also to provide protection for high-risk populations...

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Autores principales: Hollingsworth, Scott A., Noland, Cameron L., Vroom, Karin, Saha, Anasuya, Sam, Miranda, Gao, Qinshan, Zhou, Haihong, Grandy, David U., Singh, Sujata, Wen, Zhiyun, Warren, Christopher, Ma, Xiaohong Shirley, Malashock, Daniel, Galli, Jennifer, Go, Gwenny, Eddins, Michael, Mayhood, Todd, Sathiyamoorthy, Karthik, Fridman, Arthur, Raoufi, Fahimeh, Gomez-Llorente, Yacob, Patridge, Andrea, Tang, Yinyan, Chen, Shi-Juan, Bailly, Marc, Ji, Chengjie, Kingsley, Laura J., Cheng, Alan C., Geierstanger, Bernhard H., Gorman, Daniel M., Zhang, Lan, Pande, Kalyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444775/
https://www.ncbi.nlm.nih.gov/pubmed/37608223
http://dx.doi.org/10.1038/s41598-023-40919-7
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author Hollingsworth, Scott A.
Noland, Cameron L.
Vroom, Karin
Saha, Anasuya
Sam, Miranda
Gao, Qinshan
Zhou, Haihong
Grandy, David U.
Singh, Sujata
Wen, Zhiyun
Warren, Christopher
Ma, Xiaohong Shirley
Malashock, Daniel
Galli, Jennifer
Go, Gwenny
Eddins, Michael
Mayhood, Todd
Sathiyamoorthy, Karthik
Fridman, Arthur
Raoufi, Fahimeh
Gomez-Llorente, Yacob
Patridge, Andrea
Tang, Yinyan
Chen, Shi-Juan
Bailly, Marc
Ji, Chengjie
Kingsley, Laura J.
Cheng, Alan C.
Geierstanger, Bernhard H.
Gorman, Daniel M.
Zhang, Lan
Pande, Kalyan
author_facet Hollingsworth, Scott A.
Noland, Cameron L.
Vroom, Karin
Saha, Anasuya
Sam, Miranda
Gao, Qinshan
Zhou, Haihong
Grandy, David U.
Singh, Sujata
Wen, Zhiyun
Warren, Christopher
Ma, Xiaohong Shirley
Malashock, Daniel
Galli, Jennifer
Go, Gwenny
Eddins, Michael
Mayhood, Todd
Sathiyamoorthy, Karthik
Fridman, Arthur
Raoufi, Fahimeh
Gomez-Llorente, Yacob
Patridge, Andrea
Tang, Yinyan
Chen, Shi-Juan
Bailly, Marc
Ji, Chengjie
Kingsley, Laura J.
Cheng, Alan C.
Geierstanger, Bernhard H.
Gorman, Daniel M.
Zhang, Lan
Pande, Kalyan
author_sort Hollingsworth, Scott A.
collection PubMed
description Coronaviruses have been the causative agent of three epidemics and pandemics in the past two decades, including the ongoing COVID-19 pandemic. A broadly-neutralizing coronavirus therapeutic is desirable not only to prevent and treat COVID-19, but also to provide protection for high-risk populations against future emergent coronaviruses. As all coronaviruses use spike proteins on the viral surface to enter the host cells, and these spike proteins share sequence and structural homology, we set out to discover cross-reactive biologic agents targeting the spike protein to block viral entry. Through llama immunization campaigns, we have identified single domain antibodies (VHHs) that are cross-reactive against multiple emergent coronaviruses (SARS-CoV, SARS-CoV-2, and MERS). Importantly, a number of these antibodies show sub-nanomolar potency towards all SARS-like viruses including emergent CoV-2 variants. We identified nine distinct epitopes on the spike protein targeted by these VHHs. Further, by engineering VHHs targeting distinct, conserved epitopes into multi-valent formats, we significantly enhanced their neutralization potencies compared to the corresponding VHH cocktails. We believe this approach is ideally suited to address both emerging SARS-CoV-2 variants during the current pandemic as well as potential future pandemics caused by SARS-like coronaviruses.
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spelling pubmed-104447752023-08-24 Discovery and multimerization of cross-reactive single-domain antibodies against SARS-like viruses to enhance potency and address emerging SARS-CoV-2 variants Hollingsworth, Scott A. Noland, Cameron L. Vroom, Karin Saha, Anasuya Sam, Miranda Gao, Qinshan Zhou, Haihong Grandy, David U. Singh, Sujata Wen, Zhiyun Warren, Christopher Ma, Xiaohong Shirley Malashock, Daniel Galli, Jennifer Go, Gwenny Eddins, Michael Mayhood, Todd Sathiyamoorthy, Karthik Fridman, Arthur Raoufi, Fahimeh Gomez-Llorente, Yacob Patridge, Andrea Tang, Yinyan Chen, Shi-Juan Bailly, Marc Ji, Chengjie Kingsley, Laura J. Cheng, Alan C. Geierstanger, Bernhard H. Gorman, Daniel M. Zhang, Lan Pande, Kalyan Sci Rep Article Coronaviruses have been the causative agent of three epidemics and pandemics in the past two decades, including the ongoing COVID-19 pandemic. A broadly-neutralizing coronavirus therapeutic is desirable not only to prevent and treat COVID-19, but also to provide protection for high-risk populations against future emergent coronaviruses. As all coronaviruses use spike proteins on the viral surface to enter the host cells, and these spike proteins share sequence and structural homology, we set out to discover cross-reactive biologic agents targeting the spike protein to block viral entry. Through llama immunization campaigns, we have identified single domain antibodies (VHHs) that are cross-reactive against multiple emergent coronaviruses (SARS-CoV, SARS-CoV-2, and MERS). Importantly, a number of these antibodies show sub-nanomolar potency towards all SARS-like viruses including emergent CoV-2 variants. We identified nine distinct epitopes on the spike protein targeted by these VHHs. Further, by engineering VHHs targeting distinct, conserved epitopes into multi-valent formats, we significantly enhanced their neutralization potencies compared to the corresponding VHH cocktails. We believe this approach is ideally suited to address both emerging SARS-CoV-2 variants during the current pandemic as well as potential future pandemics caused by SARS-like coronaviruses. Nature Publishing Group UK 2023-08-22 /pmc/articles/PMC10444775/ /pubmed/37608223 http://dx.doi.org/10.1038/s41598-023-40919-7 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hollingsworth, Scott A.
Noland, Cameron L.
Vroom, Karin
Saha, Anasuya
Sam, Miranda
Gao, Qinshan
Zhou, Haihong
Grandy, David U.
Singh, Sujata
Wen, Zhiyun
Warren, Christopher
Ma, Xiaohong Shirley
Malashock, Daniel
Galli, Jennifer
Go, Gwenny
Eddins, Michael
Mayhood, Todd
Sathiyamoorthy, Karthik
Fridman, Arthur
Raoufi, Fahimeh
Gomez-Llorente, Yacob
Patridge, Andrea
Tang, Yinyan
Chen, Shi-Juan
Bailly, Marc
Ji, Chengjie
Kingsley, Laura J.
Cheng, Alan C.
Geierstanger, Bernhard H.
Gorman, Daniel M.
Zhang, Lan
Pande, Kalyan
Discovery and multimerization of cross-reactive single-domain antibodies against SARS-like viruses to enhance potency and address emerging SARS-CoV-2 variants
title Discovery and multimerization of cross-reactive single-domain antibodies against SARS-like viruses to enhance potency and address emerging SARS-CoV-2 variants
title_full Discovery and multimerization of cross-reactive single-domain antibodies against SARS-like viruses to enhance potency and address emerging SARS-CoV-2 variants
title_fullStr Discovery and multimerization of cross-reactive single-domain antibodies against SARS-like viruses to enhance potency and address emerging SARS-CoV-2 variants
title_full_unstemmed Discovery and multimerization of cross-reactive single-domain antibodies against SARS-like viruses to enhance potency and address emerging SARS-CoV-2 variants
title_short Discovery and multimerization of cross-reactive single-domain antibodies against SARS-like viruses to enhance potency and address emerging SARS-CoV-2 variants
title_sort discovery and multimerization of cross-reactive single-domain antibodies against sars-like viruses to enhance potency and address emerging sars-cov-2 variants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444775/
https://www.ncbi.nlm.nih.gov/pubmed/37608223
http://dx.doi.org/10.1038/s41598-023-40919-7
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