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Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods

Vero cells were grown adherent to microcarriers (Cytodex 1; 3 g L(−1)) using animal component free media in stirred-tank type bioreactors. Different strategies for media refreshment, daily media replacement (semi-batch), continuous media replacement (perfusion) and recirculation of media, were compa...

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Autores principales: Thomassen, Yvonne E., Rubingh, Olaf, Wijffels, René H., van der Pol, Leo A., Bakker, Wilfried A.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355417/
https://www.ncbi.nlm.nih.gov/pubmed/24583004
http://dx.doi.org/10.1016/j.vaccine.2014.02.022
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author Thomassen, Yvonne E.
Rubingh, Olaf
Wijffels, René H.
van der Pol, Leo A.
Bakker, Wilfried A.M.
author_facet Thomassen, Yvonne E.
Rubingh, Olaf
Wijffels, René H.
van der Pol, Leo A.
Bakker, Wilfried A.M.
author_sort Thomassen, Yvonne E.
collection PubMed
description Vero cells were grown adherent to microcarriers (Cytodex 1; 3 g L(−1)) using animal component free media in stirred-tank type bioreactors. Different strategies for media refreshment, daily media replacement (semi-batch), continuous media replacement (perfusion) and recirculation of media, were compared with batch cultivation. Cell densities increased using a feed strategy from 1 × 10(6) cells mL(−1) during batch cultivation to 1.8, 2.7 and 5.0 × 10(6) cells mL(−1) during semi-batch, perfusion and recirculation, respectively. The effects of these different cell culture strategies on subsequent poliovirus production were investigated. Increased cell densities allowed up to 3 times higher d-antigen levels when compared with that obtained from batch-wise Vero cell culture. However, the cell specific d-antigen production was lower when cells were infected at higher cell densities. This cell density effect is in good agreement with observations for different cell lines and virus types. From the evaluated alternative culture methods, application of a semi-batch mode of operations allowed the highest cell specific d-antigen production. The increased product yields that can easily be reached using these higher cell density cultivation methods, showed the possibility for better use of bioreactor capacity for the manufacturing of polio vaccines to ultimately reduce vaccine cost per dose. Further, the use of animal-component-free cell- and virus culture media shows opportunities for modernization of human viral vaccine manufacturing.
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spelling pubmed-53554172017-03-24 Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods Thomassen, Yvonne E. Rubingh, Olaf Wijffels, René H. van der Pol, Leo A. Bakker, Wilfried A.M. Vaccine Article Vero cells were grown adherent to microcarriers (Cytodex 1; 3 g L(−1)) using animal component free media in stirred-tank type bioreactors. Different strategies for media refreshment, daily media replacement (semi-batch), continuous media replacement (perfusion) and recirculation of media, were compared with batch cultivation. Cell densities increased using a feed strategy from 1 × 10(6) cells mL(−1) during batch cultivation to 1.8, 2.7 and 5.0 × 10(6) cells mL(−1) during semi-batch, perfusion and recirculation, respectively. The effects of these different cell culture strategies on subsequent poliovirus production were investigated. Increased cell densities allowed up to 3 times higher d-antigen levels when compared with that obtained from batch-wise Vero cell culture. However, the cell specific d-antigen production was lower when cells were infected at higher cell densities. This cell density effect is in good agreement with observations for different cell lines and virus types. From the evaluated alternative culture methods, application of a semi-batch mode of operations allowed the highest cell specific d-antigen production. The increased product yields that can easily be reached using these higher cell density cultivation methods, showed the possibility for better use of bioreactor capacity for the manufacturing of polio vaccines to ultimately reduce vaccine cost per dose. Further, the use of animal-component-free cell- and virus culture media shows opportunities for modernization of human viral vaccine manufacturing. Elsevier Science 2014-05-19 /pmc/articles/PMC5355417/ /pubmed/24583004 http://dx.doi.org/10.1016/j.vaccine.2014.02.022 Text en © Published by Elsevier Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Thomassen, Yvonne E.
Rubingh, Olaf
Wijffels, René H.
van der Pol, Leo A.
Bakker, Wilfried A.M.
Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods
title Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods
title_full Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods
title_fullStr Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods
title_full_unstemmed Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods
title_short Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods
title_sort improved poliovirus d-antigen yields by application of different vero cell cultivation methods
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355417/
https://www.ncbi.nlm.nih.gov/pubmed/24583004
http://dx.doi.org/10.1016/j.vaccine.2014.02.022
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