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SARS-CoV-2 mRNA Vaccine Design Enabled by Prototype Pathogen Preparedness
A severe acute respiratory syndrome coronavirus (SARS-CoV-2) vaccine is needed to control the global coronavirus infectious disease (COVID-19) public health crisis. Atomic-level structures directed the application of prefusion-stabilizing mutations that improved expression and immunogenicity of beta...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581537/ https://www.ncbi.nlm.nih.gov/pubmed/32756549 http://dx.doi.org/10.1038/s41586-020-2622-0 |
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author | Corbett, Kizzmekia S. Edwards, Darin K. Leist, Sarah R. Abiona, Olubukola M. Boyoglu-Barnum, Seyhan Gillespie, Rebecca A. Himansu, Sunny Schäfer, Alexandra Ziwawo, Cynthia T. DiPiazza, Anthony T. Dinnon, Kenneth H. Elbashir, Sayda M. Shaw, Christine A. Woods, Angela Fritch, Ethan J. Martinez, David R. Bock, Kevin W. Minai, Mahnaz Nagata, Bianca M. Hutchinson, Geoffrey B. Wu, Kai Henry, Carole Bahi, Kapil Garcia-Dominguez, Dario Ma, LingZhi Renzi, Isabella Kong, Wing-Pui Schmidt, Stephen D. Wang, Lingshu Zhang, Yi Phung, Emily Chang, Lauren A. Loomis, Rebecca J. Altaras, Nedim Emil Narayanan, Elisabeth Metkar, Mihir Presnyak, Vlad Liu, Cuiping Louder, Mark K. Shi, Wei Leung, Kwanyee Yang, Eun Sung West, Ande Gully, Kendra L. Stevens, Laura J. Wang, Nianshuang Wrapp, Daniel Doria-Rose, Nicole A. Stewart-Jones, Guillaume Bennett, Hamilton Alvarado, Gabriela S. Nason, Martha C. Ruckwardt, Tracy J. McLellan, Jason S. Denison, Mark R. Chappell, James D. Moore, Ian N. Morabito, Kaitlyn M. Mascola, John R. Baric, Ralph S. Carfi, Andrea Graham, Barney S. |
author_facet | Corbett, Kizzmekia S. Edwards, Darin K. Leist, Sarah R. Abiona, Olubukola M. Boyoglu-Barnum, Seyhan Gillespie, Rebecca A. Himansu, Sunny Schäfer, Alexandra Ziwawo, Cynthia T. DiPiazza, Anthony T. Dinnon, Kenneth H. Elbashir, Sayda M. Shaw, Christine A. Woods, Angela Fritch, Ethan J. Martinez, David R. Bock, Kevin W. Minai, Mahnaz Nagata, Bianca M. Hutchinson, Geoffrey B. Wu, Kai Henry, Carole Bahi, Kapil Garcia-Dominguez, Dario Ma, LingZhi Renzi, Isabella Kong, Wing-Pui Schmidt, Stephen D. Wang, Lingshu Zhang, Yi Phung, Emily Chang, Lauren A. Loomis, Rebecca J. Altaras, Nedim Emil Narayanan, Elisabeth Metkar, Mihir Presnyak, Vlad Liu, Cuiping Louder, Mark K. Shi, Wei Leung, Kwanyee Yang, Eun Sung West, Ande Gully, Kendra L. Stevens, Laura J. Wang, Nianshuang Wrapp, Daniel Doria-Rose, Nicole A. Stewart-Jones, Guillaume Bennett, Hamilton Alvarado, Gabriela S. Nason, Martha C. Ruckwardt, Tracy J. McLellan, Jason S. Denison, Mark R. Chappell, James D. Moore, Ian N. Morabito, Kaitlyn M. Mascola, John R. Baric, Ralph S. Carfi, Andrea Graham, Barney S. |
author_sort | Corbett, Kizzmekia S. |
collection | PubMed |
description | A severe acute respiratory syndrome coronavirus (SARS-CoV-2) vaccine is needed to control the global coronavirus infectious disease (COVID-19) public health crisis. Atomic-level structures directed the application of prefusion-stabilizing mutations that improved expression and immunogenicity of betacoronavirus spike proteins(1). Using this established immunogen design, the release of SARS-CoV-2 sequences triggered immediate rapid manufacturing of an mRNA vaccine expressing the prefusion-stabilized SARS-CoV-2 spike trimer (mRNA-1273). Here, we show that mRNA-1273 induces both potent neutralizing antibody responses to wild-type (D614) and D614G mutant(2) SARS-CoV-2 and CD8 T cell responses and protects against SARS-CoV-2 infection in lungs and noses of mice without evidence of immunopathology. mRNA-1273 is currently in Phase 3 efficacy evaluation. |
format | Online Article Text |
id | pubmed-7581537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-75815372021-02-05 SARS-CoV-2 mRNA Vaccine Design Enabled by Prototype Pathogen Preparedness Corbett, Kizzmekia S. Edwards, Darin K. Leist, Sarah R. Abiona, Olubukola M. Boyoglu-Barnum, Seyhan Gillespie, Rebecca A. Himansu, Sunny Schäfer, Alexandra Ziwawo, Cynthia T. DiPiazza, Anthony T. Dinnon, Kenneth H. Elbashir, Sayda M. Shaw, Christine A. Woods, Angela Fritch, Ethan J. Martinez, David R. Bock, Kevin W. Minai, Mahnaz Nagata, Bianca M. Hutchinson, Geoffrey B. Wu, Kai Henry, Carole Bahi, Kapil Garcia-Dominguez, Dario Ma, LingZhi Renzi, Isabella Kong, Wing-Pui Schmidt, Stephen D. Wang, Lingshu Zhang, Yi Phung, Emily Chang, Lauren A. Loomis, Rebecca J. Altaras, Nedim Emil Narayanan, Elisabeth Metkar, Mihir Presnyak, Vlad Liu, Cuiping Louder, Mark K. Shi, Wei Leung, Kwanyee Yang, Eun Sung West, Ande Gully, Kendra L. Stevens, Laura J. Wang, Nianshuang Wrapp, Daniel Doria-Rose, Nicole A. Stewart-Jones, Guillaume Bennett, Hamilton Alvarado, Gabriela S. Nason, Martha C. Ruckwardt, Tracy J. McLellan, Jason S. Denison, Mark R. Chappell, James D. Moore, Ian N. Morabito, Kaitlyn M. Mascola, John R. Baric, Ralph S. Carfi, Andrea Graham, Barney S. Nature Article A severe acute respiratory syndrome coronavirus (SARS-CoV-2) vaccine is needed to control the global coronavirus infectious disease (COVID-19) public health crisis. Atomic-level structures directed the application of prefusion-stabilizing mutations that improved expression and immunogenicity of betacoronavirus spike proteins(1). Using this established immunogen design, the release of SARS-CoV-2 sequences triggered immediate rapid manufacturing of an mRNA vaccine expressing the prefusion-stabilized SARS-CoV-2 spike trimer (mRNA-1273). Here, we show that mRNA-1273 induces both potent neutralizing antibody responses to wild-type (D614) and D614G mutant(2) SARS-CoV-2 and CD8 T cell responses and protects against SARS-CoV-2 infection in lungs and noses of mice without evidence of immunopathology. mRNA-1273 is currently in Phase 3 efficacy evaluation. 2020-08-05 2020-10 /pmc/articles/PMC7581537/ /pubmed/32756549 http://dx.doi.org/10.1038/s41586-020-2622-0 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Corbett, Kizzmekia S. Edwards, Darin K. Leist, Sarah R. Abiona, Olubukola M. Boyoglu-Barnum, Seyhan Gillespie, Rebecca A. Himansu, Sunny Schäfer, Alexandra Ziwawo, Cynthia T. DiPiazza, Anthony T. Dinnon, Kenneth H. Elbashir, Sayda M. Shaw, Christine A. Woods, Angela Fritch, Ethan J. Martinez, David R. Bock, Kevin W. Minai, Mahnaz Nagata, Bianca M. Hutchinson, Geoffrey B. Wu, Kai Henry, Carole Bahi, Kapil Garcia-Dominguez, Dario Ma, LingZhi Renzi, Isabella Kong, Wing-Pui Schmidt, Stephen D. Wang, Lingshu Zhang, Yi Phung, Emily Chang, Lauren A. Loomis, Rebecca J. Altaras, Nedim Emil Narayanan, Elisabeth Metkar, Mihir Presnyak, Vlad Liu, Cuiping Louder, Mark K. Shi, Wei Leung, Kwanyee Yang, Eun Sung West, Ande Gully, Kendra L. Stevens, Laura J. Wang, Nianshuang Wrapp, Daniel Doria-Rose, Nicole A. Stewart-Jones, Guillaume Bennett, Hamilton Alvarado, Gabriela S. Nason, Martha C. Ruckwardt, Tracy J. McLellan, Jason S. Denison, Mark R. Chappell, James D. Moore, Ian N. Morabito, Kaitlyn M. Mascola, John R. Baric, Ralph S. Carfi, Andrea Graham, Barney S. SARS-CoV-2 mRNA Vaccine Design Enabled by Prototype Pathogen Preparedness |
title | SARS-CoV-2 mRNA Vaccine Design Enabled by Prototype Pathogen Preparedness |
title_full | SARS-CoV-2 mRNA Vaccine Design Enabled by Prototype Pathogen Preparedness |
title_fullStr | SARS-CoV-2 mRNA Vaccine Design Enabled by Prototype Pathogen Preparedness |
title_full_unstemmed | SARS-CoV-2 mRNA Vaccine Design Enabled by Prototype Pathogen Preparedness |
title_short | SARS-CoV-2 mRNA Vaccine Design Enabled by Prototype Pathogen Preparedness |
title_sort | sars-cov-2 mrna vaccine design enabled by prototype pathogen preparedness |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581537/ https://www.ncbi.nlm.nih.gov/pubmed/32756549 http://dx.doi.org/10.1038/s41586-020-2622-0 |
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