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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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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. |
format | Online Article Text |
id | pubmed-3861478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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