Cargando…
Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor
The outbreak of the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes the Coronavirus Disease 2019 (COVID-19) has spread through the globe at an alarming speed. The disease has become a global pandemic affecting millions of people and created public health crises worldwi...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841742/ https://www.ncbi.nlm.nih.gov/pubmed/36687766 http://dx.doi.org/10.1016/j.btre.2023.e00782 |
_version_ | 1784869962359242752 |
---|---|
author | Ton, Christopher Stabile, Victoria Carey, Elizabeth Maraikar, Adam Whitmer, Travis Marrone, Samantha Afanador, Nelson Lee Zabrodin, Igor Manomohan, Greeshma Whiteman, Melissa Hofmann, Carl |
author_facet | Ton, Christopher Stabile, Victoria Carey, Elizabeth Maraikar, Adam Whitmer, Travis Marrone, Samantha Afanador, Nelson Lee Zabrodin, Igor Manomohan, Greeshma Whiteman, Melissa Hofmann, Carl |
author_sort | Ton, Christopher |
collection | PubMed |
description | The outbreak of the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes the Coronavirus Disease 2019 (COVID-19) has spread through the globe at an alarming speed. The disease has become a global pandemic affecting millions of people and created public health crises worldwide. Among many efforts to urgently develop a vaccine against this disease, we developed an industrial-scale closed, single use manufacturing process for V590, a vaccine candidate for SARS-CoV-2. V590 is a recombinant vesicular stomatitis virus (rVSV) genetically engineered to express SARS-CoV-2 glycoprotein. In this work, we describe the development and optimization of serum-free microcarrier production of V590 in Vero cells in a closed system. To achieve the maximum virus productivity, we optimized pH and temperature during virus production in 3 liters (L) bioreactors. Virus productivity was improved (by ∼1 log) by using pH 7.0 and temperature at 34.0 °C. The optimal production condition was successfully scaled up to a 2000 L Single Use Bioreactor (SUB), producing a maximum virus titer of ∼1.0e+7 plaque forming units (PFU)/mL. Further process intensification and simplification, including growing Vero cells at 2 gs per liter (g/L) of Cytodex-1 Gamma microcarriers and eliminating the media exchange (MX) step prior to infection helped to increase virus productivity by ∼2-fold. |
format | Online Article Text |
id | pubmed-9841742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98417422023-01-17 Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor Ton, Christopher Stabile, Victoria Carey, Elizabeth Maraikar, Adam Whitmer, Travis Marrone, Samantha Afanador, Nelson Lee Zabrodin, Igor Manomohan, Greeshma Whiteman, Melissa Hofmann, Carl Biotechnol Rep (Amst) Research Article The outbreak of the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes the Coronavirus Disease 2019 (COVID-19) has spread through the globe at an alarming speed. The disease has become a global pandemic affecting millions of people and created public health crises worldwide. Among many efforts to urgently develop a vaccine against this disease, we developed an industrial-scale closed, single use manufacturing process for V590, a vaccine candidate for SARS-CoV-2. V590 is a recombinant vesicular stomatitis virus (rVSV) genetically engineered to express SARS-CoV-2 glycoprotein. In this work, we describe the development and optimization of serum-free microcarrier production of V590 in Vero cells in a closed system. To achieve the maximum virus productivity, we optimized pH and temperature during virus production in 3 liters (L) bioreactors. Virus productivity was improved (by ∼1 log) by using pH 7.0 and temperature at 34.0 °C. The optimal production condition was successfully scaled up to a 2000 L Single Use Bioreactor (SUB), producing a maximum virus titer of ∼1.0e+7 plaque forming units (PFU)/mL. Further process intensification and simplification, including growing Vero cells at 2 gs per liter (g/L) of Cytodex-1 Gamma microcarriers and eliminating the media exchange (MX) step prior to infection helped to increase virus productivity by ∼2-fold. Elsevier 2023-01-16 /pmc/articles/PMC9841742/ /pubmed/36687766 http://dx.doi.org/10.1016/j.btre.2023.e00782 Text en © 2023 Merck Sharp & Dohme LLC., a subsidiary Merck & Co., Inc., Rahway, NJ, USA and The Author(s). Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Ton, Christopher Stabile, Victoria Carey, Elizabeth Maraikar, Adam Whitmer, Travis Marrone, Samantha Afanador, Nelson Lee Zabrodin, Igor Manomohan, Greeshma Whiteman, Melissa Hofmann, Carl Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor |
title | Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor |
title_full | Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor |
title_fullStr | Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor |
title_full_unstemmed | Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor |
title_short | Development and scale-up of rVSV-SARS-CoV-2 vaccine process using single use bioreactor |
title_sort | development and scale-up of rvsv-sars-cov-2 vaccine process using single use bioreactor |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841742/ https://www.ncbi.nlm.nih.gov/pubmed/36687766 http://dx.doi.org/10.1016/j.btre.2023.e00782 |
work_keys_str_mv | AT tonchristopher developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT stabilevictoria developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT careyelizabeth developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT maraikaradam developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT whitmertravis developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT marronesamantha developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT afanadornelsonlee developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT zabrodinigor developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT manomohangreeshma developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT whitemanmelissa developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor AT hofmanncarl developmentandscaleupofrvsvsarscov2vaccineprocessusingsingleusebioreactor |