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Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens

The preferred product characteristics (for chemistry, control, and manufacture), in addition to safety and efficacy, are quintessential requirements for any successful therapeutic. Messenger RNA vaccines constitute a relatively new alternative to traditional vaccine development platforms, and thus t...

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Detalles Bibliográficos
Autores principales: Poveda, Cristina, Biter, Amadeo B., Bottazzi, Maria Elena, Strych, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963847/
https://www.ncbi.nlm.nih.gov/pubmed/31569760
http://dx.doi.org/10.3390/vaccines7040131
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author Poveda, Cristina
Biter, Amadeo B.
Bottazzi, Maria Elena
Strych, Ulrich
author_facet Poveda, Cristina
Biter, Amadeo B.
Bottazzi, Maria Elena
Strych, Ulrich
author_sort Poveda, Cristina
collection PubMed
description The preferred product characteristics (for chemistry, control, and manufacture), in addition to safety and efficacy, are quintessential requirements for any successful therapeutic. Messenger RNA vaccines constitute a relatively new alternative to traditional vaccine development platforms, and thus there is less clarity regarding the criteria needed to ensure regulatory compliance and acceptance. Generally, to identify the ideal product characteristics, a series of assays needs to be developed, qualified and ultimately validated to determine the integrity, purity, stability, and reproducibility of a vaccine target. Here, using the available literature, we provide a summary of the array of biophysical and biochemical assays currently used in the field to characterize mRNA vaccine antigen candidates. Moreover, we review various in vitro functional cell-based assays that have been employed to facilitate the early assessment of the biological activity of these molecules, including the predictive immune response triggered in the host cell. Messenger RNA vaccines can be produced rapidly and at large scale, and thus will particularly benefit from well-defined and well-characterized assays ultimately to be used for in-process, release and stability-indications, which will allow equally rapid screening of immunogenicity, efficacy, and safety without the need to conduct often lengthy and costly in vivo experiments.
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spelling pubmed-69638472020-01-27 Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens Poveda, Cristina Biter, Amadeo B. Bottazzi, Maria Elena Strych, Ulrich Vaccines (Basel) Review The preferred product characteristics (for chemistry, control, and manufacture), in addition to safety and efficacy, are quintessential requirements for any successful therapeutic. Messenger RNA vaccines constitute a relatively new alternative to traditional vaccine development platforms, and thus there is less clarity regarding the criteria needed to ensure regulatory compliance and acceptance. Generally, to identify the ideal product characteristics, a series of assays needs to be developed, qualified and ultimately validated to determine the integrity, purity, stability, and reproducibility of a vaccine target. Here, using the available literature, we provide a summary of the array of biophysical and biochemical assays currently used in the field to characterize mRNA vaccine antigen candidates. Moreover, we review various in vitro functional cell-based assays that have been employed to facilitate the early assessment of the biological activity of these molecules, including the predictive immune response triggered in the host cell. Messenger RNA vaccines can be produced rapidly and at large scale, and thus will particularly benefit from well-defined and well-characterized assays ultimately to be used for in-process, release and stability-indications, which will allow equally rapid screening of immunogenicity, efficacy, and safety without the need to conduct often lengthy and costly in vivo experiments. MDPI 2019-09-27 /pmc/articles/PMC6963847/ /pubmed/31569760 http://dx.doi.org/10.3390/vaccines7040131 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Poveda, Cristina
Biter, Amadeo B.
Bottazzi, Maria Elena
Strych, Ulrich
Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens
title Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens
title_full Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens
title_fullStr Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens
title_full_unstemmed Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens
title_short Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens
title_sort establishing preferred product characterization for the evaluation of rna vaccine antigens
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963847/
https://www.ncbi.nlm.nih.gov/pubmed/31569760
http://dx.doi.org/10.3390/vaccines7040131
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