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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2020
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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. |
format | Online Article Text |
id | pubmed-7373143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
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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