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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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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. |
format | Online Article Text |
id | pubmed-7337387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
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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