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The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies

Monoclonal antibodies against SARS-CoV-2 are a clinically validated therapeutic option against COVID-19. Because rapidly emerging virus mutants are becoming the next major concern in the fight against the global pandemic, it is imperative that these therapeutic treatments provide coverage against ci...

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Autores principales: Copin, Richard, Baum, Alina, Wloga, Elzbieta, Pascal, Kristen E., Giordano, Stephanie, Fulton, Benjamin O., Zhou, Anbo, Negron, Nicole, Lanza, Kathryn, Chan, Newton, Coppola, Angel, Chiu, Joyce, Ni, Min, Wei, Yi, Atwal, Gurinder S., Hernandez, Annabel Romero, Saotome, Kei, Zhou, Yi, Franklin, Matthew C., Hooper, Andrea T., McCarthy, Shane, Hamon, Sara, Hamilton, Jennifer D., Staples, Hilary M., Alfson, Kendra, Carrion, Ricardo, Ali, Shazia, Norton, Thomas, Somersan-Karakaya, Selin, Sivapalasingam, Sumathi, Herman, Gary A., Weinreich, David M., Lipsich, Leah, Stahl, Neil, Murphy, Andrew J., Yancopoulos, George D., Kyratsous, Christos A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179113/
https://www.ncbi.nlm.nih.gov/pubmed/34161776
http://dx.doi.org/10.1016/j.cell.2021.06.002
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author Copin, Richard
Baum, Alina
Wloga, Elzbieta
Pascal, Kristen E.
Giordano, Stephanie
Fulton, Benjamin O.
Zhou, Anbo
Negron, Nicole
Lanza, Kathryn
Chan, Newton
Coppola, Angel
Chiu, Joyce
Ni, Min
Wei, Yi
Atwal, Gurinder S.
Hernandez, Annabel Romero
Saotome, Kei
Zhou, Yi
Franklin, Matthew C.
Hooper, Andrea T.
McCarthy, Shane
Hamon, Sara
Hamilton, Jennifer D.
Staples, Hilary M.
Alfson, Kendra
Carrion, Ricardo
Ali, Shazia
Norton, Thomas
Somersan-Karakaya, Selin
Sivapalasingam, Sumathi
Herman, Gary A.
Weinreich, David M.
Lipsich, Leah
Stahl, Neil
Murphy, Andrew J.
Yancopoulos, George D.
Kyratsous, Christos A.
author_facet Copin, Richard
Baum, Alina
Wloga, Elzbieta
Pascal, Kristen E.
Giordano, Stephanie
Fulton, Benjamin O.
Zhou, Anbo
Negron, Nicole
Lanza, Kathryn
Chan, Newton
Coppola, Angel
Chiu, Joyce
Ni, Min
Wei, Yi
Atwal, Gurinder S.
Hernandez, Annabel Romero
Saotome, Kei
Zhou, Yi
Franklin, Matthew C.
Hooper, Andrea T.
McCarthy, Shane
Hamon, Sara
Hamilton, Jennifer D.
Staples, Hilary M.
Alfson, Kendra
Carrion, Ricardo
Ali, Shazia
Norton, Thomas
Somersan-Karakaya, Selin
Sivapalasingam, Sumathi
Herman, Gary A.
Weinreich, David M.
Lipsich, Leah
Stahl, Neil
Murphy, Andrew J.
Yancopoulos, George D.
Kyratsous, Christos A.
author_sort Copin, Richard
collection PubMed
description Monoclonal antibodies against SARS-CoV-2 are a clinically validated therapeutic option against COVID-19. Because rapidly emerging virus mutants are becoming the next major concern in the fight against the global pandemic, it is imperative that these therapeutic treatments provide coverage against circulating variants and do not contribute to development of treatment-induced emergent resistance. To this end, we investigated the sequence diversity of the spike protein and monitored emergence of virus variants in SARS-COV-2 isolates found in COVID-19 patients treated with the two-antibody combination REGEN-COV, as well as in preclinical in vitro studies using single, dual, or triple antibody combinations, and in hamster in vivo studies using REGEN-COV or single monoclonal antibody treatments. Our study demonstrates that the combination of non-competing antibodies in REGEN-COV provides protection against all current SARS-CoV-2 variants of concern/interest and also protects against emergence of new variants and their potential seeding into the population in a clinical setting.
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spelling pubmed-81791132021-06-05 The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies Copin, Richard Baum, Alina Wloga, Elzbieta Pascal, Kristen E. Giordano, Stephanie Fulton, Benjamin O. Zhou, Anbo Negron, Nicole Lanza, Kathryn Chan, Newton Coppola, Angel Chiu, Joyce Ni, Min Wei, Yi Atwal, Gurinder S. Hernandez, Annabel Romero Saotome, Kei Zhou, Yi Franklin, Matthew C. Hooper, Andrea T. McCarthy, Shane Hamon, Sara Hamilton, Jennifer D. Staples, Hilary M. Alfson, Kendra Carrion, Ricardo Ali, Shazia Norton, Thomas Somersan-Karakaya, Selin Sivapalasingam, Sumathi Herman, Gary A. Weinreich, David M. Lipsich, Leah Stahl, Neil Murphy, Andrew J. Yancopoulos, George D. Kyratsous, Christos A. Cell Article Monoclonal antibodies against SARS-CoV-2 are a clinically validated therapeutic option against COVID-19. Because rapidly emerging virus mutants are becoming the next major concern in the fight against the global pandemic, it is imperative that these therapeutic treatments provide coverage against circulating variants and do not contribute to development of treatment-induced emergent resistance. To this end, we investigated the sequence diversity of the spike protein and monitored emergence of virus variants in SARS-COV-2 isolates found in COVID-19 patients treated with the two-antibody combination REGEN-COV, as well as in preclinical in vitro studies using single, dual, or triple antibody combinations, and in hamster in vivo studies using REGEN-COV or single monoclonal antibody treatments. Our study demonstrates that the combination of non-competing antibodies in REGEN-COV provides protection against all current SARS-CoV-2 variants of concern/interest and also protects against emergence of new variants and their potential seeding into the population in a clinical setting. The Author(s). Published by Elsevier Inc. 2021-07-22 2021-06-05 /pmc/articles/PMC8179113/ /pubmed/34161776 http://dx.doi.org/10.1016/j.cell.2021.06.002 Text en © 2021 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
Copin, Richard
Baum, Alina
Wloga, Elzbieta
Pascal, Kristen E.
Giordano, Stephanie
Fulton, Benjamin O.
Zhou, Anbo
Negron, Nicole
Lanza, Kathryn
Chan, Newton
Coppola, Angel
Chiu, Joyce
Ni, Min
Wei, Yi
Atwal, Gurinder S.
Hernandez, Annabel Romero
Saotome, Kei
Zhou, Yi
Franklin, Matthew C.
Hooper, Andrea T.
McCarthy, Shane
Hamon, Sara
Hamilton, Jennifer D.
Staples, Hilary M.
Alfson, Kendra
Carrion, Ricardo
Ali, Shazia
Norton, Thomas
Somersan-Karakaya, Selin
Sivapalasingam, Sumathi
Herman, Gary A.
Weinreich, David M.
Lipsich, Leah
Stahl, Neil
Murphy, Andrew J.
Yancopoulos, George D.
Kyratsous, Christos A.
The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies
title The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies
title_full The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies
title_fullStr The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies
title_full_unstemmed The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies
title_short The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies
title_sort monoclonal antibody combination regen-cov protects against sars-cov-2 mutational escape in preclinical and human studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179113/
https://www.ncbi.nlm.nih.gov/pubmed/34161776
http://dx.doi.org/10.1016/j.cell.2021.06.002
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