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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ton, Christopher, Stabile, Victoria, Carey, Elizabeth, Maraikar, Adam, Whitmer, Travis, Marrone, Samantha, Afanador, Nelson Lee, Zabrodin, Igor, Manomohan, Greeshma, Whiteman, Melissa, Hofmann, Carl
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