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Functional profiling of Covid 19 vaccine candidate by flow virometry
Vaccine development is a complex process, starting with selection of a promising immunogen in the discovery phase, followed by process development in the preclinical phase, and later by clinical trials in tandem with process improvements and scale up. A large suite of analytical techniques is requir...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359933/ https://www.ncbi.nlm.nih.gov/pubmed/35985887 http://dx.doi.org/10.1016/j.vaccine.2022.08.006 |
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author | Prout, Ashley Rustandi, Richard R. Tubbs, Christopher Winters, Michael A. McKenna, Philip Vlasak, Josef |
author_facet | Prout, Ashley Rustandi, Richard R. Tubbs, Christopher Winters, Michael A. McKenna, Philip Vlasak, Josef |
author_sort | Prout, Ashley |
collection | PubMed |
description | Vaccine development is a complex process, starting with selection of a promising immunogen in the discovery phase, followed by process development in the preclinical phase, and later by clinical trials in tandem with process improvements and scale up. A large suite of analytical techniques is required to gain understanding of the vaccine candidate so that a relevant immunogen is selected and subsequently manufactured consistently throughout the lifespan of the product. For viral vaccines, successful immunogen production is contingent on its maintained antigenicity and/or infectivity, as well as the ability to characterize these qualities within the context of the process, formulation, and clinical performance. In this report we show the utility of flow virometry during preclinical development of a Covid 19 vaccine candidate based on SARS-CoV-2 spike (S) protein expressed on vesicular stomatitis virus (VSV). Using a panel of monoclonal antibodies, we were able to detect the S protein on the surface of the recombinant VSV virus, monitor the expression levels, detect differences in the antigen based on S protein sequence and after virus inactivation, and monitor S protein stability. Collectively, flow virometry provided important data that helped to guide preclinical development of this vaccine candidate. |
format | Online Article Text |
id | pubmed-9359933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93599332022-08-09 Functional profiling of Covid 19 vaccine candidate by flow virometry Prout, Ashley Rustandi, Richard R. Tubbs, Christopher Winters, Michael A. McKenna, Philip Vlasak, Josef Vaccine Article Vaccine development is a complex process, starting with selection of a promising immunogen in the discovery phase, followed by process development in the preclinical phase, and later by clinical trials in tandem with process improvements and scale up. A large suite of analytical techniques is required to gain understanding of the vaccine candidate so that a relevant immunogen is selected and subsequently manufactured consistently throughout the lifespan of the product. For viral vaccines, successful immunogen production is contingent on its maintained antigenicity and/or infectivity, as well as the ability to characterize these qualities within the context of the process, formulation, and clinical performance. In this report we show the utility of flow virometry during preclinical development of a Covid 19 vaccine candidate based on SARS-CoV-2 spike (S) protein expressed on vesicular stomatitis virus (VSV). Using a panel of monoclonal antibodies, we were able to detect the S protein on the surface of the recombinant VSV virus, monitor the expression levels, detect differences in the antigen based on S protein sequence and after virus inactivation, and monitor S protein stability. Collectively, flow virometry provided important data that helped to guide preclinical development of this vaccine candidate. Elsevier Ltd. 2022-09-02 2022-08-09 /pmc/articles/PMC9359933/ /pubmed/35985887 http://dx.doi.org/10.1016/j.vaccine.2022.08.006 Text en © 2022 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Prout, Ashley Rustandi, Richard R. Tubbs, Christopher Winters, Michael A. McKenna, Philip Vlasak, Josef Functional profiling of Covid 19 vaccine candidate by flow virometry |
title | Functional profiling of Covid 19 vaccine candidate by flow virometry |
title_full | Functional profiling of Covid 19 vaccine candidate by flow virometry |
title_fullStr | Functional profiling of Covid 19 vaccine candidate by flow virometry |
title_full_unstemmed | Functional profiling of Covid 19 vaccine candidate by flow virometry |
title_short | Functional profiling of Covid 19 vaccine candidate by flow virometry |
title_sort | functional profiling of covid 19 vaccine candidate by flow virometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359933/ https://www.ncbi.nlm.nih.gov/pubmed/35985887 http://dx.doi.org/10.1016/j.vaccine.2022.08.006 |
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