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Identifying COVID-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling

INTRODUCTION: Identifying optimal COVID-19 vaccine dose is essential for maximizing their impact. However, COVID-19 vaccine dose-finding has been an empirical process, limited by short development timeframes, and therefore potentially not thoroughly investigated. Mathematical IS/ID modelling is a no...

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Autores principales: Rhodes, Sophie, Smith, Neal, Evans, Thomas, White, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574467/
https://www.ncbi.nlm.nih.gov/pubmed/36272876
http://dx.doi.org/10.1016/j.vaccine.2022.10.012
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author Rhodes, Sophie
Smith, Neal
Evans, Thomas
White, Richard
author_facet Rhodes, Sophie
Smith, Neal
Evans, Thomas
White, Richard
author_sort Rhodes, Sophie
collection PubMed
description INTRODUCTION: Identifying optimal COVID-19 vaccine dose is essential for maximizing their impact. However, COVID-19 vaccine dose-finding has been an empirical process, limited by short development timeframes, and therefore potentially not thoroughly investigated. Mathematical IS/ID modelling is a novel method for predicting optimal vaccine dose which could inform future COVID-19 vaccine dose decision making. METHODS: Published clinical data on COVID-19 vaccine dose–response was identified and extracted. Mathematical models were calibrated to the dose–response data stratified by subpopulation, where possible to predict optimal dose. Predicted optimal doses were summarised across vaccine type and compared to chosen dose for the primary series of COVID-19 vaccines to identify vaccine doses that may benefit from re-evaluation. RESULTS: 30 clinical dose–response datasets in adults and elderly population were extracted for four vaccine types and optimal doses predicted using the models. Results suggest that, if re-assessed for dose, COVID-19 vaccines Ad26.cov, ChadOx1 n-Cov19, BNT162b2, Coronavac, and NVX-CoV2373 could benefit from increased dose in adults and mRNA-1273 and Coronavac, could benefit from increased and decreased dose for the elderly population, respectively. DISCUSSION: Future iterations of COVID-19 vaccines could benefit from re-evaluating dose to ensure most effective use of the vaccine and mathematical modelling can support this.
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spelling pubmed-95744672022-10-17 Identifying COVID-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling Rhodes, Sophie Smith, Neal Evans, Thomas White, Richard Vaccine Article INTRODUCTION: Identifying optimal COVID-19 vaccine dose is essential for maximizing their impact. However, COVID-19 vaccine dose-finding has been an empirical process, limited by short development timeframes, and therefore potentially not thoroughly investigated. Mathematical IS/ID modelling is a novel method for predicting optimal vaccine dose which could inform future COVID-19 vaccine dose decision making. METHODS: Published clinical data on COVID-19 vaccine dose–response was identified and extracted. Mathematical models were calibrated to the dose–response data stratified by subpopulation, where possible to predict optimal dose. Predicted optimal doses were summarised across vaccine type and compared to chosen dose for the primary series of COVID-19 vaccines to identify vaccine doses that may benefit from re-evaluation. RESULTS: 30 clinical dose–response datasets in adults and elderly population were extracted for four vaccine types and optimal doses predicted using the models. Results suggest that, if re-assessed for dose, COVID-19 vaccines Ad26.cov, ChadOx1 n-Cov19, BNT162b2, Coronavac, and NVX-CoV2373 could benefit from increased dose in adults and mRNA-1273 and Coronavac, could benefit from increased and decreased dose for the elderly population, respectively. DISCUSSION: Future iterations of COVID-19 vaccines could benefit from re-evaluating dose to ensure most effective use of the vaccine and mathematical modelling can support this. Published by Elsevier Ltd. 2022-11-22 2022-10-17 /pmc/articles/PMC9574467/ /pubmed/36272876 http://dx.doi.org/10.1016/j.vaccine.2022.10.012 Text en © 2022 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Rhodes, Sophie
Smith, Neal
Evans, Thomas
White, Richard
Identifying COVID-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling
title Identifying COVID-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling
title_full Identifying COVID-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling
title_fullStr Identifying COVID-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling
title_full_unstemmed Identifying COVID-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling
title_short Identifying COVID-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling
title_sort identifying covid-19 optimal vaccine dose using mathematical immunostimulation/immunodynamic modelling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574467/
https://www.ncbi.nlm.nih.gov/pubmed/36272876
http://dx.doi.org/10.1016/j.vaccine.2022.10.012
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