Cargando…
Characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation
Adenovirus vectors offer a platform technology for vaccine development. The value of the platform has been proven during the COVID-19 pandemic. Although good stability at 2–8 °C is an advantage of the platform, non-cold-chain distribution would have substantial advantages, in particular in low-incom...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536692/ https://www.ncbi.nlm.nih.gov/pubmed/34686689 http://dx.doi.org/10.1038/s41598-021-00065-4 |
_version_ | 1784588074504683520 |
---|---|
author | Dulal, Pawan Gharaei, Robabeh Berg, Adam Walters, Adam A. Hawkins, Nicholas Claridge, Tim D. W. Kowal, Katarzyna Neill, Steven Ritchie, Adam J. Ashfield, Rebecca Hill, Adrian V. S. Tronci, Giuseppe Russell, Stephen J. Douglas, Alexander D. |
author_facet | Dulal, Pawan Gharaei, Robabeh Berg, Adam Walters, Adam A. Hawkins, Nicholas Claridge, Tim D. W. Kowal, Katarzyna Neill, Steven Ritchie, Adam J. Ashfield, Rebecca Hill, Adrian V. S. Tronci, Giuseppe Russell, Stephen J. Douglas, Alexander D. |
author_sort | Dulal, Pawan |
collection | PubMed |
description | Adenovirus vectors offer a platform technology for vaccine development. The value of the platform has been proven during the COVID-19 pandemic. Although good stability at 2–8 °C is an advantage of the platform, non-cold-chain distribution would have substantial advantages, in particular in low-income countries. We have previously reported a novel, potentially less expensive thermostabilisation approach using a combination of simple sugars and glass micro-fibrous matrix, achieving excellent recovery of adenovirus-vectored vaccines after storage at temperatures as high as 45 °C. This matrix is, however, prone to fragmentation and so not suitable for clinical translation. Here, we report an investigation of alternative fibrous matrices which might be suitable for clinical use. A number of commercially-available matrices permitted good protein recovery, quality of sugar glass and moisture content of the dried product but did not achieve the thermostabilisation performance of the original glass fibre matrix. We therefore further investigated physical and chemical characteristics of the glass fibre matrix and its components, finding that the polyvinyl alcohol present in the glass fibre matrix assists vaccine stability. This finding enabled us to identify a potentially biocompatible matrix with encouraging performance. We discuss remaining challenges for transfer of the technology into clinical use, including reliability of process performance. |
format | Online Article Text |
id | pubmed-8536692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85366922021-10-25 Characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation Dulal, Pawan Gharaei, Robabeh Berg, Adam Walters, Adam A. Hawkins, Nicholas Claridge, Tim D. W. Kowal, Katarzyna Neill, Steven Ritchie, Adam J. Ashfield, Rebecca Hill, Adrian V. S. Tronci, Giuseppe Russell, Stephen J. Douglas, Alexander D. Sci Rep Article Adenovirus vectors offer a platform technology for vaccine development. The value of the platform has been proven during the COVID-19 pandemic. Although good stability at 2–8 °C is an advantage of the platform, non-cold-chain distribution would have substantial advantages, in particular in low-income countries. We have previously reported a novel, potentially less expensive thermostabilisation approach using a combination of simple sugars and glass micro-fibrous matrix, achieving excellent recovery of adenovirus-vectored vaccines after storage at temperatures as high as 45 °C. This matrix is, however, prone to fragmentation and so not suitable for clinical translation. Here, we report an investigation of alternative fibrous matrices which might be suitable for clinical use. A number of commercially-available matrices permitted good protein recovery, quality of sugar glass and moisture content of the dried product but did not achieve the thermostabilisation performance of the original glass fibre matrix. We therefore further investigated physical and chemical characteristics of the glass fibre matrix and its components, finding that the polyvinyl alcohol present in the glass fibre matrix assists vaccine stability. This finding enabled us to identify a potentially biocompatible matrix with encouraging performance. We discuss remaining challenges for transfer of the technology into clinical use, including reliability of process performance. Nature Publishing Group UK 2021-10-22 /pmc/articles/PMC8536692/ /pubmed/34686689 http://dx.doi.org/10.1038/s41598-021-00065-4 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Dulal, Pawan Gharaei, Robabeh Berg, Adam Walters, Adam A. Hawkins, Nicholas Claridge, Tim D. W. Kowal, Katarzyna Neill, Steven Ritchie, Adam J. Ashfield, Rebecca Hill, Adrian V. S. Tronci, Giuseppe Russell, Stephen J. Douglas, Alexander D. Characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation |
title | Characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation |
title_full | Characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation |
title_fullStr | Characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation |
title_full_unstemmed | Characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation |
title_short | Characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation |
title_sort | characterisation of factors contributing to the performance of nonwoven fibrous matrices as substrates for adenovirus vectored vaccine stabilisation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536692/ https://www.ncbi.nlm.nih.gov/pubmed/34686689 http://dx.doi.org/10.1038/s41598-021-00065-4 |
work_keys_str_mv | AT dulalpawan characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT gharaeirobabeh characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT bergadam characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT waltersadama characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT hawkinsnicholas characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT claridgetimdw characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT kowalkatarzyna characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT neillsteven characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT ritchieadamj characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT ashfieldrebecca characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT hilladrianvs characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT troncigiuseppe characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT russellstephenj characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation AT douglasalexanderd characterisationoffactorscontributingtotheperformanceofnonwovenfibrousmatricesassubstratesforadenovirusvectoredvaccinestabilisation |