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Developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine
Despite solid evidence of the success of rotavirus vaccines in saving children from fatal gastroenteritis, more than 82 million infants worldwide still lack access to a rotavirus vaccine. The main barriers to global rotavirus vaccine coverage include cost, manufacturing capacity and suboptimal effic...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062787/ https://www.ncbi.nlm.nih.gov/pubmed/33744044 http://dx.doi.org/10.1016/j.vaccine.2021.03.033 |
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author | Hamidi, Ahd Hoeksema, Femke Velthof, Pim Lemckert, Angelique Gillissen, Gert Luitjens, Alfred Bines, Julie E. Pullagurla, Swathi R. Kumar, Prashant Volkin, David B. Joshi, Sangeeta B. Havenga, Menzo Bakker, Wilfried A.M. Yallop, Christopher |
author_facet | Hamidi, Ahd Hoeksema, Femke Velthof, Pim Lemckert, Angelique Gillissen, Gert Luitjens, Alfred Bines, Julie E. Pullagurla, Swathi R. Kumar, Prashant Volkin, David B. Joshi, Sangeeta B. Havenga, Menzo Bakker, Wilfried A.M. Yallop, Christopher |
author_sort | Hamidi, Ahd |
collection | PubMed |
description | Despite solid evidence of the success of rotavirus vaccines in saving children from fatal gastroenteritis, more than 82 million infants worldwide still lack access to a rotavirus vaccine. The main barriers to global rotavirus vaccine coverage include cost, manufacturing capacity and suboptimal efficacy in low- and lower-middle income countries. One vaccine candidate with the potential to address the latter is based on the novel, naturally attenuated RV3 strain of rotavirus, RV3-BB vaccine administered in a birth dose strategy had a vaccine efficacy against severe rotavirus gastroenteritis of 94% at 12 months of age in infants in Indonesia. To further develop this vaccine candidate, a well-documented and low-cost manufacturing process is required. A target fully loaded cost of goods (COGs) of ≤$3.50 per course of three doses was set based on predicted market requirements. COGs modelling was leveraged to develop a process using Vero cells in cell factories reaching high titers, reducing or replacing expensive reagents and shortening process time to maximise output. Stable candidate liquid formulations were developed allowing two-year storage at 2–8 °C. In addition, the formulation potentially renders needless the pretreatment of vaccinees with antacid to ensure adequate gastric acid neutralization for routine oral vaccination. As a result, the formulation allows small volume dosing and reduction of supply chain costs. A dose ranging study is currently underway in Malawi that will inform the final clinical dose required. At a clinical dose of ≤6.3 log(10) FFU, the COGs target of ≤$3.50 per three dose course was met. At a clinical dose of 6.5 log(10) FFU, the final manufacturing process resulted in a COGs that is substantially lower than the current average market price, 2.44 USD per dose. The manufacturing and formulation processes were transferred to BioFarma in Indonesia to enable future RV3-BB vaccine production. |
format | Online Article Text |
id | pubmed-8062787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-80627872021-04-27 Developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine Hamidi, Ahd Hoeksema, Femke Velthof, Pim Lemckert, Angelique Gillissen, Gert Luitjens, Alfred Bines, Julie E. Pullagurla, Swathi R. Kumar, Prashant Volkin, David B. Joshi, Sangeeta B. Havenga, Menzo Bakker, Wilfried A.M. Yallop, Christopher Vaccine Article Despite solid evidence of the success of rotavirus vaccines in saving children from fatal gastroenteritis, more than 82 million infants worldwide still lack access to a rotavirus vaccine. The main barriers to global rotavirus vaccine coverage include cost, manufacturing capacity and suboptimal efficacy in low- and lower-middle income countries. One vaccine candidate with the potential to address the latter is based on the novel, naturally attenuated RV3 strain of rotavirus, RV3-BB vaccine administered in a birth dose strategy had a vaccine efficacy against severe rotavirus gastroenteritis of 94% at 12 months of age in infants in Indonesia. To further develop this vaccine candidate, a well-documented and low-cost manufacturing process is required. A target fully loaded cost of goods (COGs) of ≤$3.50 per course of three doses was set based on predicted market requirements. COGs modelling was leveraged to develop a process using Vero cells in cell factories reaching high titers, reducing or replacing expensive reagents and shortening process time to maximise output. Stable candidate liquid formulations were developed allowing two-year storage at 2–8 °C. In addition, the formulation potentially renders needless the pretreatment of vaccinees with antacid to ensure adequate gastric acid neutralization for routine oral vaccination. As a result, the formulation allows small volume dosing and reduction of supply chain costs. A dose ranging study is currently underway in Malawi that will inform the final clinical dose required. At a clinical dose of ≤6.3 log(10) FFU, the COGs target of ≤$3.50 per three dose course was met. At a clinical dose of 6.5 log(10) FFU, the final manufacturing process resulted in a COGs that is substantially lower than the current average market price, 2.44 USD per dose. The manufacturing and formulation processes were transferred to BioFarma in Indonesia to enable future RV3-BB vaccine production. Elsevier Science 2021-04-08 /pmc/articles/PMC8062787/ /pubmed/33744044 http://dx.doi.org/10.1016/j.vaccine.2021.03.033 Text en © 2021 Batavia Biosciences BV https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hamidi, Ahd Hoeksema, Femke Velthof, Pim Lemckert, Angelique Gillissen, Gert Luitjens, Alfred Bines, Julie E. Pullagurla, Swathi R. Kumar, Prashant Volkin, David B. Joshi, Sangeeta B. Havenga, Menzo Bakker, Wilfried A.M. Yallop, Christopher Developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine |
title | Developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine |
title_full | Developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine |
title_fullStr | Developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine |
title_full_unstemmed | Developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine |
title_short | Developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine |
title_sort | developing a manufacturing process to deliver a cost effective and stable liquid human rotavirus vaccine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062787/ https://www.ncbi.nlm.nih.gov/pubmed/33744044 http://dx.doi.org/10.1016/j.vaccine.2021.03.033 |
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