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A novel SARS-CoV-2 subunit vaccine engineered on an immune-activating platform technology
While there are several SARS-CoV-2 vaccines currently available, additional options must be provided that are safe, effective, and affordable for the entire global population. We have developed a novel immune activating platform technology that will fill this need. This recombinant platform protein...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721441/ https://www.ncbi.nlm.nih.gov/pubmed/35801956 http://dx.doi.org/10.1080/21645515.2022.2062971 |
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author | Quinlan, Edward J. Chubet, Richard Leonardi, Peter |
author_facet | Quinlan, Edward J. Chubet, Richard Leonardi, Peter |
author_sort | Quinlan, Edward J. |
collection | PubMed |
description | While there are several SARS-CoV-2 vaccines currently available, additional options must be provided that are safe, effective, and affordable for the entire global population. We have developed a novel immune activating platform technology that will fill this need. This recombinant platform protein is produced in insect cells using baculoviral expression technology similar to what is currently used for several other approved vaccines as well as employed by myriad GMP facilities globally. Thus, infrastructure exists for rapid scale up following initial optimizations. Here we report initial results for a SARS-CoV-2 vaccine (OMN008) based on our platform technology. Unadjuvanted OMN008 vaccination resulted in robust antigenicity and neutralization. Additionally, OMN008 vaccination induced a specific CD8 T-cell response. All of these results taken together indicate OMN008 may be an excellent candidate to fill gaps left by the currently available vaccines. Further testing is necessary to fully optimize production; however, overall cost of production should remain low given the simple formulation of this recombinant platform. |
format | Online Article Text |
id | pubmed-9721441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-97214412022-12-06 A novel SARS-CoV-2 subunit vaccine engineered on an immune-activating platform technology Quinlan, Edward J. Chubet, Richard Leonardi, Peter Hum Vaccin Immunother ISV Annual Congress SF – Short Report While there are several SARS-CoV-2 vaccines currently available, additional options must be provided that are safe, effective, and affordable for the entire global population. We have developed a novel immune activating platform technology that will fill this need. This recombinant platform protein is produced in insect cells using baculoviral expression technology similar to what is currently used for several other approved vaccines as well as employed by myriad GMP facilities globally. Thus, infrastructure exists for rapid scale up following initial optimizations. Here we report initial results for a SARS-CoV-2 vaccine (OMN008) based on our platform technology. Unadjuvanted OMN008 vaccination resulted in robust antigenicity and neutralization. Additionally, OMN008 vaccination induced a specific CD8 T-cell response. All of these results taken together indicate OMN008 may be an excellent candidate to fill gaps left by the currently available vaccines. Further testing is necessary to fully optimize production; however, overall cost of production should remain low given the simple formulation of this recombinant platform. Taylor & Francis 2022-07-08 /pmc/articles/PMC9721441/ /pubmed/35801956 http://dx.doi.org/10.1080/21645515.2022.2062971 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | ISV Annual Congress SF – Short Report Quinlan, Edward J. Chubet, Richard Leonardi, Peter A novel SARS-CoV-2 subunit vaccine engineered on an immune-activating platform technology |
title | A novel SARS-CoV-2 subunit vaccine engineered on an immune-activating platform technology |
title_full | A novel SARS-CoV-2 subunit vaccine engineered on an immune-activating platform technology |
title_fullStr | A novel SARS-CoV-2 subunit vaccine engineered on an immune-activating platform technology |
title_full_unstemmed | A novel SARS-CoV-2 subunit vaccine engineered on an immune-activating platform technology |
title_short | A novel SARS-CoV-2 subunit vaccine engineered on an immune-activating platform technology |
title_sort | novel sars-cov-2 subunit vaccine engineered on an immune-activating platform technology |
topic | ISV Annual Congress SF – Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721441/ https://www.ncbi.nlm.nih.gov/pubmed/35801956 http://dx.doi.org/10.1080/21645515.2022.2062971 |
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