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Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform

Modified Vaccinia Ankara (MVA) is a highly attenuated poxvirus vector that is widely used to develop vaccines for infectious diseases and cancer. We developed a novel vaccine platform based on a unique three-plasmid system to efficiently generate recombinant MVA vectors from chemically synthesized D...

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Autores principales: Chiuppesi, Flavia, Salazar, Marcela d’Alincourt, Contreras, Heidi, Nguyen, Vu, Martinez, Joy, Park, Soojin, Nguyen, Jenny, Kha, Mindy, Iniguez, Angelina, Zhou, Qiao, Kaltcheva, Teodora, Levytskyy, Roman, Ebelt, Nancy, Kang, Tae, Wu, Xiwei, Rogers, Tom, Manuel, Edwin, Shostak, Yuriy, Diamond, Don, Wussow, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373143/
https://www.ncbi.nlm.nih.gov/pubmed/32702732
http://dx.doi.org/10.21203/rs.3.rs-40198/v1
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author Chiuppesi, Flavia
Salazar, Marcela d’Alincourt
Contreras, Heidi
Nguyen, Vu
Martinez, Joy
Park, Soojin
Nguyen, Jenny
Kha, Mindy
Iniguez, Angelina
Zhou, Qiao
Kaltcheva, Teodora
Levytskyy, Roman
Ebelt, Nancy
Kang, Tae
Wu, Xiwei
Rogers, Tom
Manuel, Edwin
Shostak, Yuriy
Diamond, Don
Wussow, Felix
author_facet Chiuppesi, Flavia
Salazar, Marcela d’Alincourt
Contreras, Heidi
Nguyen, Vu
Martinez, Joy
Park, Soojin
Nguyen, Jenny
Kha, Mindy
Iniguez, Angelina
Zhou, Qiao
Kaltcheva, Teodora
Levytskyy, Roman
Ebelt, Nancy
Kang, Tae
Wu, Xiwei
Rogers, Tom
Manuel, Edwin
Shostak, Yuriy
Diamond, Don
Wussow, Felix
author_sort Chiuppesi, Flavia
collection PubMed
description Modified Vaccinia Ankara (MVA) is a highly attenuated poxvirus vector that is widely used to develop vaccines for infectious diseases and cancer. We developed a novel vaccine platform based on a unique three-plasmid system to efficiently generate recombinant MVA vectors from chemically synthesized DNA. In response to the ongoing global pandemic caused by SARS coronavirus-2 (SARS-CoV-2), we used this novel vaccine platform to rapidly produce fully synthetic MVA (sMVA) vectors co-expressing SARS-CoV-2 spike and nucleocapsid antigens, two immunodominant antigens implicated in protective immunity. Mice immunized with these sMVA vectors developed robust SARS-CoV-2 antigen-specific humoral and cellular immune responses, including potent neutralizing antibodies. These results demonstrate the potential of a novel vaccine platform based on synthetic DNA to efficiently generate recombinant MVA vectors and to rapidly develop a multi-antigenic poxvirus-based SARS-CoV-2 vaccine candidate.
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spelling pubmed-73731432020-07-22 Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform Chiuppesi, Flavia Salazar, Marcela d’Alincourt Contreras, Heidi Nguyen, Vu Martinez, Joy Park, Soojin Nguyen, Jenny Kha, Mindy Iniguez, Angelina Zhou, Qiao Kaltcheva, Teodora Levytskyy, Roman Ebelt, Nancy Kang, Tae Wu, Xiwei Rogers, Tom Manuel, Edwin Shostak, Yuriy Diamond, Don Wussow, Felix Res Sq Article Modified Vaccinia Ankara (MVA) is a highly attenuated poxvirus vector that is widely used to develop vaccines for infectious diseases and cancer. We developed a novel vaccine platform based on a unique three-plasmid system to efficiently generate recombinant MVA vectors from chemically synthesized DNA. In response to the ongoing global pandemic caused by SARS coronavirus-2 (SARS-CoV-2), we used this novel vaccine platform to rapidly produce fully synthetic MVA (sMVA) vectors co-expressing SARS-CoV-2 spike and nucleocapsid antigens, two immunodominant antigens implicated in protective immunity. Mice immunized with these sMVA vectors developed robust SARS-CoV-2 antigen-specific humoral and cellular immune responses, including potent neutralizing antibodies. These results demonstrate the potential of a novel vaccine platform based on synthetic DNA to efficiently generate recombinant MVA vectors and to rapidly develop a multi-antigenic poxvirus-based SARS-CoV-2 vaccine candidate. American Journal Experts 2020-07-17 /pmc/articles/PMC7373143/ /pubmed/32702732 http://dx.doi.org/10.21203/rs.3.rs-40198/v1 Text en This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Chiuppesi, Flavia
Salazar, Marcela d’Alincourt
Contreras, Heidi
Nguyen, Vu
Martinez, Joy
Park, Soojin
Nguyen, Jenny
Kha, Mindy
Iniguez, Angelina
Zhou, Qiao
Kaltcheva, Teodora
Levytskyy, Roman
Ebelt, Nancy
Kang, Tae
Wu, Xiwei
Rogers, Tom
Manuel, Edwin
Shostak, Yuriy
Diamond, Don
Wussow, Felix
Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform
title Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform
title_full Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform
title_fullStr Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform
title_full_unstemmed Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform
title_short Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform
title_sort development of a multi-antigenic sars-cov-2 vaccine using a synthetic poxvirus platform
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373143/
https://www.ncbi.nlm.nih.gov/pubmed/32702732
http://dx.doi.org/10.21203/rs.3.rs-40198/v1
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