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Next Generation Inactivated Polio Vaccine Manufacturing to Support Post Polio-Eradication Biosafety Goals

Worldwide efforts to eradicate polio caused a tipping point in polio vaccination strategies. A switch from the oral polio vaccine, which can cause circulating and virulent vaccine derived polioviruses, to inactivated polio vaccines (IPV) is scheduled. Moreover, a manufacturing process, using attenua...

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Autores principales: Thomassen, Yvonne E., van ’t Oever, Aart G., van Oijen, Monique G. C. T., Wijffels, René H., van der Pol, Leo A., Bakker, Wilfried A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861478/
https://www.ncbi.nlm.nih.gov/pubmed/24349497
http://dx.doi.org/10.1371/journal.pone.0083374
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author Thomassen, Yvonne E.
van ’t Oever, Aart G.
van Oijen, Monique G. C. T.
Wijffels, René H.
van der Pol, Leo A.
Bakker, Wilfried A. M.
author_facet Thomassen, Yvonne E.
van ’t Oever, Aart G.
van Oijen, Monique G. C. T.
Wijffels, René H.
van der Pol, Leo A.
Bakker, Wilfried A. M.
author_sort Thomassen, Yvonne E.
collection PubMed
description Worldwide efforts to eradicate polio caused a tipping point in polio vaccination strategies. A switch from the oral polio vaccine, which can cause circulating and virulent vaccine derived polioviruses, to inactivated polio vaccines (IPV) is scheduled. Moreover, a manufacturing process, using attenuated virus strains instead of wild-type polioviruses, is demanded to enhance worldwide production of IPV, especially in low- and middle income countries. Therefore, development of an IPV from attenuated (Sabin) poliovirus strains (sIPV) was pursued. Starting from the current IPV production process based on wild type Salk strains, adaptations, such as lower virus cultivation temperature, were implemented. sIPV was produced at industrial scale followed by formulation of both plain and aluminium adjuvanted sIPV. The final products met the quality criteria, were immunogenic in rats, showed no toxicity in rabbits and could be released for testing in the clinic. Concluding, sIPV was developed to manufacturing scale. The technology can be transferred worldwide to support post polio-eradication biosafety goals.
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spelling pubmed-38614782013-12-17 Next Generation Inactivated Polio Vaccine Manufacturing to Support Post Polio-Eradication Biosafety Goals Thomassen, Yvonne E. van ’t Oever, Aart G. van Oijen, Monique G. C. T. Wijffels, René H. van der Pol, Leo A. Bakker, Wilfried A. M. PLoS One Research Article Worldwide efforts to eradicate polio caused a tipping point in polio vaccination strategies. A switch from the oral polio vaccine, which can cause circulating and virulent vaccine derived polioviruses, to inactivated polio vaccines (IPV) is scheduled. Moreover, a manufacturing process, using attenuated virus strains instead of wild-type polioviruses, is demanded to enhance worldwide production of IPV, especially in low- and middle income countries. Therefore, development of an IPV from attenuated (Sabin) poliovirus strains (sIPV) was pursued. Starting from the current IPV production process based on wild type Salk strains, adaptations, such as lower virus cultivation temperature, were implemented. sIPV was produced at industrial scale followed by formulation of both plain and aluminium adjuvanted sIPV. The final products met the quality criteria, were immunogenic in rats, showed no toxicity in rabbits and could be released for testing in the clinic. Concluding, sIPV was developed to manufacturing scale. The technology can be transferred worldwide to support post polio-eradication biosafety goals. Public Library of Science 2013-12-12 /pmc/articles/PMC3861478/ /pubmed/24349497 http://dx.doi.org/10.1371/journal.pone.0083374 Text en © 2013 Thomassen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Thomassen, Yvonne E.
van ’t Oever, Aart G.
van Oijen, Monique G. C. T.
Wijffels, René H.
van der Pol, Leo A.
Bakker, Wilfried A. M.
Next Generation Inactivated Polio Vaccine Manufacturing to Support Post Polio-Eradication Biosafety Goals
title Next Generation Inactivated Polio Vaccine Manufacturing to Support Post Polio-Eradication Biosafety Goals
title_full Next Generation Inactivated Polio Vaccine Manufacturing to Support Post Polio-Eradication Biosafety Goals
title_fullStr Next Generation Inactivated Polio Vaccine Manufacturing to Support Post Polio-Eradication Biosafety Goals
title_full_unstemmed Next Generation Inactivated Polio Vaccine Manufacturing to Support Post Polio-Eradication Biosafety Goals
title_short Next Generation Inactivated Polio Vaccine Manufacturing to Support Post Polio-Eradication Biosafety Goals
title_sort next generation inactivated polio vaccine manufacturing to support post polio-eradication biosafety goals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861478/
https://www.ncbi.nlm.nih.gov/pubmed/24349497
http://dx.doi.org/10.1371/journal.pone.0083374
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