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Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals
Neutralizing monoclonal antibodies (mAbs) targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Spike glycoprotein have been developed for the treatment of COVID-19. Whilst antibody therapy has been shown to reduce the risk of COVID-19-associated hospitalization and death, there is...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9914479/ https://www.ncbi.nlm.nih.gov/pubmed/36844257 http://dx.doi.org/10.1093/oxfimm/iqac012 |
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author | Kurshan, Ashwini Snell, Luke B Prior, Lucie Tam, Jerry C H Graham, Carl Thangarajah, Rajeni Edgeworth, Jonathan D Nebbia, Gaia Doores, Katie J |
author_facet | Kurshan, Ashwini Snell, Luke B Prior, Lucie Tam, Jerry C H Graham, Carl Thangarajah, Rajeni Edgeworth, Jonathan D Nebbia, Gaia Doores, Katie J |
author_sort | Kurshan, Ashwini |
collection | PubMed |
description | Neutralizing monoclonal antibodies (mAbs) targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Spike glycoprotein have been developed for the treatment of COVID-19. Whilst antibody therapy has been shown to reduce the risk of COVID-19-associated hospitalization and death, there is limited understanding of the endogenous immunity to SARS-CoV-2 generated in mAb-treated patients and therefore ongoing susceptibility to future infections. Here we measure the endogenous antibody response in SARS-CoV-2-infected individuals treated with REGN-COV2 (Ronapreve). We show that in the majority of unvaccinated, delta-infected REGN-COV2-treated individuals, an endogenous antibody response is generated, but, like untreated, delta-infected individuals, there was a limited neutralization breadth. However, some vaccinated individuals who were seronegative at SARS-CoV-2 infection baseline and some unvaccinated individuals failed to produce an endogenous immune response following infection and REGN-COV2 treatment demonstrating the importance of mAb therapy in some patient populations. |
format | Online Article Text |
id | pubmed-9914479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99144792023-02-24 Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals Kurshan, Ashwini Snell, Luke B Prior, Lucie Tam, Jerry C H Graham, Carl Thangarajah, Rajeni Edgeworth, Jonathan D Nebbia, Gaia Doores, Katie J Oxf Open Immunol Research Article Neutralizing monoclonal antibodies (mAbs) targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Spike glycoprotein have been developed for the treatment of COVID-19. Whilst antibody therapy has been shown to reduce the risk of COVID-19-associated hospitalization and death, there is limited understanding of the endogenous immunity to SARS-CoV-2 generated in mAb-treated patients and therefore ongoing susceptibility to future infections. Here we measure the endogenous antibody response in SARS-CoV-2-infected individuals treated with REGN-COV2 (Ronapreve). We show that in the majority of unvaccinated, delta-infected REGN-COV2-treated individuals, an endogenous antibody response is generated, but, like untreated, delta-infected individuals, there was a limited neutralization breadth. However, some vaccinated individuals who were seronegative at SARS-CoV-2 infection baseline and some unvaccinated individuals failed to produce an endogenous immune response following infection and REGN-COV2 treatment demonstrating the importance of mAb therapy in some patient populations. Oxford University Press 2023-01-06 /pmc/articles/PMC9914479/ /pubmed/36844257 http://dx.doi.org/10.1093/oxfimm/iqac012 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kurshan, Ashwini Snell, Luke B Prior, Lucie Tam, Jerry C H Graham, Carl Thangarajah, Rajeni Edgeworth, Jonathan D Nebbia, Gaia Doores, Katie J Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals |
title | Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals |
title_full | Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals |
title_fullStr | Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals |
title_full_unstemmed | Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals |
title_short | Endogenous antibody responses in REGN-COV2-treated SARS-CoV-2-infected individuals |
title_sort | endogenous antibody responses in regn-cov2-treated sars-cov-2-infected individuals |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9914479/ https://www.ncbi.nlm.nih.gov/pubmed/36844257 http://dx.doi.org/10.1093/oxfimm/iqac012 |
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