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A Therapeutic Non-self-reactive SARS-CoV-2 Antibody Protects from Lung Pathology in a COVID-19 Hamster Model

The emergence of SARS-CoV-2 led to pandemic spread of coronavirus disease 2019 (COVID-19), manifesting with respiratory symptoms and multi-organ dysfunction. Detailed characterization of virus-neutralizing antibodies and target epitopes is needed to understand COVID-19 pathophysiology and guide immu...

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Autores principales: Kreye, Jakob, Reincke, S. Momsen, Kornau, Hans-Christian, Sánchez-Sendin, Elisa, Corman, Victor Max, Liu, Hejun, Yuan, Meng, Wu, Nicholas C., Zhu, Xueyong, Lee, Chang-Chun D., Trimpert, Jakob, Höltje, Markus, Dietert, Kristina, Stöffler, Laura, von Wardenburg, Niels, van Hoof, Scott, Homeyer, Marie A., Hoffmann, Julius, Abdelgawad, Azza, Gruber, Achim D., Bertzbach, Luca D., Vladimirova, Daria, Li, Lucie Y., Barthel, Paula Charlotte, Skriner, Karl, Hocke, Andreas C., Hippenstiel, Stefan, Witzenrath, Martin, Suttorp, Norbert, Kurth, Florian, Franke, Christiana, Endres, Matthias, Schmitz, Dietmar, Jeworowski, Lara Maria, Richter, Anja, Schmidt, Marie Luisa, Schwarz, Tatjana, Müller, Marcel Alexander, Drosten, Christian, Wendisch, Daniel, Sander, Leif E., Osterrieder, Nikolaus, Wilson, Ian A., Prüss, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510528/
https://www.ncbi.nlm.nih.gov/pubmed/33058755
http://dx.doi.org/10.1016/j.cell.2020.09.049
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author Kreye, Jakob
Reincke, S. Momsen
Kornau, Hans-Christian
Sánchez-Sendin, Elisa
Corman, Victor Max
Liu, Hejun
Yuan, Meng
Wu, Nicholas C.
Zhu, Xueyong
Lee, Chang-Chun D.
Trimpert, Jakob
Höltje, Markus
Dietert, Kristina
Stöffler, Laura
von Wardenburg, Niels
van Hoof, Scott
Homeyer, Marie A.
Hoffmann, Julius
Abdelgawad, Azza
Gruber, Achim D.
Bertzbach, Luca D.
Vladimirova, Daria
Li, Lucie Y.
Barthel, Paula Charlotte
Skriner, Karl
Hocke, Andreas C.
Hippenstiel, Stefan
Witzenrath, Martin
Suttorp, Norbert
Kurth, Florian
Franke, Christiana
Endres, Matthias
Schmitz, Dietmar
Jeworowski, Lara Maria
Richter, Anja
Schmidt, Marie Luisa
Schwarz, Tatjana
Müller, Marcel Alexander
Drosten, Christian
Wendisch, Daniel
Sander, Leif E.
Osterrieder, Nikolaus
Wilson, Ian A.
Prüss, Harald
author_facet Kreye, Jakob
Reincke, S. Momsen
Kornau, Hans-Christian
Sánchez-Sendin, Elisa
Corman, Victor Max
Liu, Hejun
Yuan, Meng
Wu, Nicholas C.
Zhu, Xueyong
Lee, Chang-Chun D.
Trimpert, Jakob
Höltje, Markus
Dietert, Kristina
Stöffler, Laura
von Wardenburg, Niels
van Hoof, Scott
Homeyer, Marie A.
Hoffmann, Julius
Abdelgawad, Azza
Gruber, Achim D.
Bertzbach, Luca D.
Vladimirova, Daria
Li, Lucie Y.
Barthel, Paula Charlotte
Skriner, Karl
Hocke, Andreas C.
Hippenstiel, Stefan
Witzenrath, Martin
Suttorp, Norbert
Kurth, Florian
Franke, Christiana
Endres, Matthias
Schmitz, Dietmar
Jeworowski, Lara Maria
Richter, Anja
Schmidt, Marie Luisa
Schwarz, Tatjana
Müller, Marcel Alexander
Drosten, Christian
Wendisch, Daniel
Sander, Leif E.
Osterrieder, Nikolaus
Wilson, Ian A.
Prüss, Harald
author_sort Kreye, Jakob
collection PubMed
description The emergence of SARS-CoV-2 led to pandemic spread of coronavirus disease 2019 (COVID-19), manifesting with respiratory symptoms and multi-organ dysfunction. Detailed characterization of virus-neutralizing antibodies and target epitopes is needed to understand COVID-19 pathophysiology and guide immunization strategies. Among 598 human monoclonal antibodies (mAbs) from 10 COVID-19 patients, we identified 40 strongly neutralizing mAbs. The most potent mAb, CV07-209, neutralized authentic SARS-CoV-2 with an IC(50) value of 3.1 ng/mL. Crystal structures of two mAbs in complex with the SARS-CoV-2 receptor-binding domain at 2.55 and 2.70 Å revealed a direct block of ACE2 attachment. Interestingly, some of the near-germline SARS-CoV-2-neutralizing mAbs reacted with mammalian self-antigens. Prophylactic and therapeutic application of CV07-209 protected hamsters from SARS-CoV-2 infection, weight loss, and lung pathology. Our results show that non-self-reactive virus-neutralizing mAbs elicited during SARS-CoV-2 infection are a promising therapeutic strategy.
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spelling pubmed-75105282020-09-24 A Therapeutic Non-self-reactive SARS-CoV-2 Antibody Protects from Lung Pathology in a COVID-19 Hamster Model Kreye, Jakob Reincke, S. Momsen Kornau, Hans-Christian Sánchez-Sendin, Elisa Corman, Victor Max Liu, Hejun Yuan, Meng Wu, Nicholas C. Zhu, Xueyong Lee, Chang-Chun D. Trimpert, Jakob Höltje, Markus Dietert, Kristina Stöffler, Laura von Wardenburg, Niels van Hoof, Scott Homeyer, Marie A. Hoffmann, Julius Abdelgawad, Azza Gruber, Achim D. Bertzbach, Luca D. Vladimirova, Daria Li, Lucie Y. Barthel, Paula Charlotte Skriner, Karl Hocke, Andreas C. Hippenstiel, Stefan Witzenrath, Martin Suttorp, Norbert Kurth, Florian Franke, Christiana Endres, Matthias Schmitz, Dietmar Jeworowski, Lara Maria Richter, Anja Schmidt, Marie Luisa Schwarz, Tatjana Müller, Marcel Alexander Drosten, Christian Wendisch, Daniel Sander, Leif E. Osterrieder, Nikolaus Wilson, Ian A. Prüss, Harald Cell Article The emergence of SARS-CoV-2 led to pandemic spread of coronavirus disease 2019 (COVID-19), manifesting with respiratory symptoms and multi-organ dysfunction. Detailed characterization of virus-neutralizing antibodies and target epitopes is needed to understand COVID-19 pathophysiology and guide immunization strategies. Among 598 human monoclonal antibodies (mAbs) from 10 COVID-19 patients, we identified 40 strongly neutralizing mAbs. The most potent mAb, CV07-209, neutralized authentic SARS-CoV-2 with an IC(50) value of 3.1 ng/mL. Crystal structures of two mAbs in complex with the SARS-CoV-2 receptor-binding domain at 2.55 and 2.70 Å revealed a direct block of ACE2 attachment. Interestingly, some of the near-germline SARS-CoV-2-neutralizing mAbs reacted with mammalian self-antigens. Prophylactic and therapeutic application of CV07-209 protected hamsters from SARS-CoV-2 infection, weight loss, and lung pathology. Our results show that non-self-reactive virus-neutralizing mAbs elicited during SARS-CoV-2 infection are a promising therapeutic strategy. Cell Press 2020-11-12 /pmc/articles/PMC7510528/ /pubmed/33058755 http://dx.doi.org/10.1016/j.cell.2020.09.049 Text en © 2020 The Authors http://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
Kreye, Jakob
Reincke, S. Momsen
Kornau, Hans-Christian
Sánchez-Sendin, Elisa
Corman, Victor Max
Liu, Hejun
Yuan, Meng
Wu, Nicholas C.
Zhu, Xueyong
Lee, Chang-Chun D.
Trimpert, Jakob
Höltje, Markus
Dietert, Kristina
Stöffler, Laura
von Wardenburg, Niels
van Hoof, Scott
Homeyer, Marie A.
Hoffmann, Julius
Abdelgawad, Azza
Gruber, Achim D.
Bertzbach, Luca D.
Vladimirova, Daria
Li, Lucie Y.
Barthel, Paula Charlotte
Skriner, Karl
Hocke, Andreas C.
Hippenstiel, Stefan
Witzenrath, Martin
Suttorp, Norbert
Kurth, Florian
Franke, Christiana
Endres, Matthias
Schmitz, Dietmar
Jeworowski, Lara Maria
Richter, Anja
Schmidt, Marie Luisa
Schwarz, Tatjana
Müller, Marcel Alexander
Drosten, Christian
Wendisch, Daniel
Sander, Leif E.
Osterrieder, Nikolaus
Wilson, Ian A.
Prüss, Harald
A Therapeutic Non-self-reactive SARS-CoV-2 Antibody Protects from Lung Pathology in a COVID-19 Hamster Model
title A Therapeutic Non-self-reactive SARS-CoV-2 Antibody Protects from Lung Pathology in a COVID-19 Hamster Model
title_full A Therapeutic Non-self-reactive SARS-CoV-2 Antibody Protects from Lung Pathology in a COVID-19 Hamster Model
title_fullStr A Therapeutic Non-self-reactive SARS-CoV-2 Antibody Protects from Lung Pathology in a COVID-19 Hamster Model
title_full_unstemmed A Therapeutic Non-self-reactive SARS-CoV-2 Antibody Protects from Lung Pathology in a COVID-19 Hamster Model
title_short A Therapeutic Non-self-reactive SARS-CoV-2 Antibody Protects from Lung Pathology in a COVID-19 Hamster Model
title_sort therapeutic non-self-reactive sars-cov-2 antibody protects from lung pathology in a covid-19 hamster model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510528/
https://www.ncbi.nlm.nih.gov/pubmed/33058755
http://dx.doi.org/10.1016/j.cell.2020.09.049
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