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Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine

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 H, Martinez, Joy, Park, Soojin, Nguyen, Jenny, Kha, Mindy, Iniguez, Angelina, Zhou, Qiao, Kaltcheva, Teodora, Levytskyy, Roman, Ebelt, Nancy D, Kang, Tae Hyuk, Wu, Xiwei, Rogers, Thomas, Manuel, Edwin R, Shostak, Yuriy, Diamond, Don J, Wussow, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337387/
https://www.ncbi.nlm.nih.gov/pubmed/32637957
http://dx.doi.org/10.1101/2020.07.01.183236
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author Chiuppesi, Flavia
Salazar, Marcela d’Alincourt
Contreras, Heidi
Nguyen, Vu H
Martinez, Joy
Park, Soojin
Nguyen, Jenny
Kha, Mindy
Iniguez, Angelina
Zhou, Qiao
Kaltcheva, Teodora
Levytskyy, Roman
Ebelt, Nancy D
Kang, Tae Hyuk
Wu, Xiwei
Rogers, Thomas
Manuel, Edwin R
Shostak, Yuriy
Diamond, Don J
Wussow, Felix
author_facet Chiuppesi, Flavia
Salazar, Marcela d’Alincourt
Contreras, Heidi
Nguyen, Vu H
Martinez, Joy
Park, Soojin
Nguyen, Jenny
Kha, Mindy
Iniguez, Angelina
Zhou, Qiao
Kaltcheva, Teodora
Levytskyy, Roman
Ebelt, Nancy D
Kang, Tae Hyuk
Wu, Xiwei
Rogers, Thomas
Manuel, Edwin R
Shostak, Yuriy
Diamond, Don J
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-73373872020-07-07 Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine Chiuppesi, Flavia Salazar, Marcela d’Alincourt Contreras, Heidi Nguyen, Vu H Martinez, Joy Park, Soojin Nguyen, Jenny Kha, Mindy Iniguez, Angelina Zhou, Qiao Kaltcheva, Teodora Levytskyy, Roman Ebelt, Nancy D Kang, Tae Hyuk Wu, Xiwei Rogers, Thomas Manuel, Edwin R Shostak, Yuriy Diamond, Don J Wussow, Felix bioRxiv 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. Cold Spring Harbor Laboratory 2020-07-02 /pmc/articles/PMC7337387/ /pubmed/32637957 http://dx.doi.org/10.1101/2020.07.01.183236 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Chiuppesi, Flavia
Salazar, Marcela d’Alincourt
Contreras, Heidi
Nguyen, Vu H
Martinez, Joy
Park, Soojin
Nguyen, Jenny
Kha, Mindy
Iniguez, Angelina
Zhou, Qiao
Kaltcheva, Teodora
Levytskyy, Roman
Ebelt, Nancy D
Kang, Tae Hyuk
Wu, Xiwei
Rogers, Thomas
Manuel, Edwin R
Shostak, Yuriy
Diamond, Don J
Wussow, Felix
Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine
title Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine
title_full Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine
title_fullStr Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine
title_full_unstemmed Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine
title_short Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine
title_sort development of a synthetic poxvirus-based sars-cov-2 vaccine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337387/
https://www.ncbi.nlm.nih.gov/pubmed/32637957
http://dx.doi.org/10.1101/2020.07.01.183236
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