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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...

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Autores principales: Quinlan, Edward J., Chubet, Richard, Leonardi, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
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.
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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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