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Availability and use of Standards in vaccine development
Reference materials are critical in assay development for calibrating and assessing their suitability. The devasting nature of the COVID-19 pandemic and subsequent proliferation of vaccine platforms and technologies has meant that there is even a greater need for standards for immunoassay developmen...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313826/ https://www.ncbi.nlm.nih.gov/pubmed/37391580 http://dx.doi.org/10.1038/s41541-023-00692-0 |
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author | Avumegah, Michael Selorm Mattiuzzo, Giada Särnefält, Anna Page, Mark Makar, Karen Lathey, Janet Kim, June Yimer, Solomon Abebe Craig, Danielle Knezevic, Ivana Bernasconi, Valentina Kristiansen, Paul A. Kromann, Ingrid |
author_facet | Avumegah, Michael Selorm Mattiuzzo, Giada Särnefält, Anna Page, Mark Makar, Karen Lathey, Janet Kim, June Yimer, Solomon Abebe Craig, Danielle Knezevic, Ivana Bernasconi, Valentina Kristiansen, Paul A. Kromann, Ingrid |
author_sort | Avumegah, Michael Selorm |
collection | PubMed |
description | Reference materials are critical in assay development for calibrating and assessing their suitability. The devasting nature of the COVID-19 pandemic and subsequent proliferation of vaccine platforms and technologies has meant that there is even a greater need for standards for immunoassay development, which are critical to assess and compare vaccines’ responses. Equally important are the standards needed to control the vaccine manufacturing processes. Standardized vaccine characterization assays throughout process development are essential for a successful Chemistry, Manufacturing and Controls (CMC) strategy. In this perspective paper, we advocate for reference material incorporation into assays and their calibration to International Standards from preclinical vaccine development through control testing and provide insight into why this is necessary. We also provide information on the availability of WHO international antibody standards for CEPI-priority pathogens. |
format | Online Article Text |
id | pubmed-10313826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103138262023-07-02 Availability and use of Standards in vaccine development Avumegah, Michael Selorm Mattiuzzo, Giada Särnefält, Anna Page, Mark Makar, Karen Lathey, Janet Kim, June Yimer, Solomon Abebe Craig, Danielle Knezevic, Ivana Bernasconi, Valentina Kristiansen, Paul A. Kromann, Ingrid NPJ Vaccines Perspective Reference materials are critical in assay development for calibrating and assessing their suitability. The devasting nature of the COVID-19 pandemic and subsequent proliferation of vaccine platforms and technologies has meant that there is even a greater need for standards for immunoassay development, which are critical to assess and compare vaccines’ responses. Equally important are the standards needed to control the vaccine manufacturing processes. Standardized vaccine characterization assays throughout process development are essential for a successful Chemistry, Manufacturing and Controls (CMC) strategy. In this perspective paper, we advocate for reference material incorporation into assays and their calibration to International Standards from preclinical vaccine development through control testing and provide insight into why this is necessary. We also provide information on the availability of WHO international antibody standards for CEPI-priority pathogens. Nature Publishing Group UK 2023-06-30 /pmc/articles/PMC10313826/ /pubmed/37391580 http://dx.doi.org/10.1038/s41541-023-00692-0 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Perspective Avumegah, Michael Selorm Mattiuzzo, Giada Särnefält, Anna Page, Mark Makar, Karen Lathey, Janet Kim, June Yimer, Solomon Abebe Craig, Danielle Knezevic, Ivana Bernasconi, Valentina Kristiansen, Paul A. Kromann, Ingrid Availability and use of Standards in vaccine development |
title | Availability and use of Standards in vaccine development |
title_full | Availability and use of Standards in vaccine development |
title_fullStr | Availability and use of Standards in vaccine development |
title_full_unstemmed | Availability and use of Standards in vaccine development |
title_short | Availability and use of Standards in vaccine development |
title_sort | availability and use of standards in vaccine development |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313826/ https://www.ncbi.nlm.nih.gov/pubmed/37391580 http://dx.doi.org/10.1038/s41541-023-00692-0 |
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