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Scientific rationale for developing potent RBD-based vaccines targeting COVID-19

Vaccination of the global population against COVID-19 is a great scientific, logistical, and moral challenge. Despite the rapid development and authorization of several full-length Spike (S) protein vaccines, the global demand outweighs the current supply and there is a need for safe, potent, high-v...

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Autores principales: Kleanthous, Harry, Silverman, Judith Maxwell, Makar, Karen W., Yoon, In-Kyu, Jackson, Nicholas, Vaughn, David W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553742/
https://www.ncbi.nlm.nih.gov/pubmed/34711846
http://dx.doi.org/10.1038/s41541-021-00393-6
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author Kleanthous, Harry
Silverman, Judith Maxwell
Makar, Karen W.
Yoon, In-Kyu
Jackson, Nicholas
Vaughn, David W.
author_facet Kleanthous, Harry
Silverman, Judith Maxwell
Makar, Karen W.
Yoon, In-Kyu
Jackson, Nicholas
Vaughn, David W.
author_sort Kleanthous, Harry
collection PubMed
description Vaccination of the global population against COVID-19 is a great scientific, logistical, and moral challenge. Despite the rapid development and authorization of several full-length Spike (S) protein vaccines, the global demand outweighs the current supply and there is a need for safe, potent, high-volume, affordable vaccines that can fill this gap, especially in low- and middle-income countries. Whether SARS-CoV-2 S-protein receptor-binding domain (RBD)-based vaccines could fill this gap has been debated, especially with regards to its suitability to protect against emerging viral variants of concern. Given a predominance for elicitation of neutralizing antibodies (nAbs) that target RBD following natural infection or vaccination, a key biomarker of protection, there is merit for selection of RBD as a sole vaccine immunogen. With its high-yielding production and manufacturing potential, RBD-based vaccines offer an abundance of temperature-stable doses at an affordable cost. In addition, as the RBD preferentially focuses the immune response to potent and recently recognized cross-protective determinants, this domain may be central to the development of future pan-sarbecovirus vaccines. In this study, we review the data supporting the non-inferiority of RBD as a vaccine immunogen compared to full-length S-protein vaccines with respect to humoral and cellular immune responses against both the prototype pandemic SARS-CoV-2 isolate and emerging variants of concern.
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spelling pubmed-85537422021-10-29 Scientific rationale for developing potent RBD-based vaccines targeting COVID-19 Kleanthous, Harry Silverman, Judith Maxwell Makar, Karen W. Yoon, In-Kyu Jackson, Nicholas Vaughn, David W. NPJ Vaccines Review Article Vaccination of the global population against COVID-19 is a great scientific, logistical, and moral challenge. Despite the rapid development and authorization of several full-length Spike (S) protein vaccines, the global demand outweighs the current supply and there is a need for safe, potent, high-volume, affordable vaccines that can fill this gap, especially in low- and middle-income countries. Whether SARS-CoV-2 S-protein receptor-binding domain (RBD)-based vaccines could fill this gap has been debated, especially with regards to its suitability to protect against emerging viral variants of concern. Given a predominance for elicitation of neutralizing antibodies (nAbs) that target RBD following natural infection or vaccination, a key biomarker of protection, there is merit for selection of RBD as a sole vaccine immunogen. With its high-yielding production and manufacturing potential, RBD-based vaccines offer an abundance of temperature-stable doses at an affordable cost. In addition, as the RBD preferentially focuses the immune response to potent and recently recognized cross-protective determinants, this domain may be central to the development of future pan-sarbecovirus vaccines. In this study, we review the data supporting the non-inferiority of RBD as a vaccine immunogen compared to full-length S-protein vaccines with respect to humoral and cellular immune responses against both the prototype pandemic SARS-CoV-2 isolate and emerging variants of concern. Nature Publishing Group UK 2021-10-28 /pmc/articles/PMC8553742/ /pubmed/34711846 http://dx.doi.org/10.1038/s41541-021-00393-6 Text en © The Author(s) 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 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 Review Article
Kleanthous, Harry
Silverman, Judith Maxwell
Makar, Karen W.
Yoon, In-Kyu
Jackson, Nicholas
Vaughn, David W.
Scientific rationale for developing potent RBD-based vaccines targeting COVID-19
title Scientific rationale for developing potent RBD-based vaccines targeting COVID-19
title_full Scientific rationale for developing potent RBD-based vaccines targeting COVID-19
title_fullStr Scientific rationale for developing potent RBD-based vaccines targeting COVID-19
title_full_unstemmed Scientific rationale for developing potent RBD-based vaccines targeting COVID-19
title_short Scientific rationale for developing potent RBD-based vaccines targeting COVID-19
title_sort scientific rationale for developing potent rbd-based vaccines targeting covid-19
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553742/
https://www.ncbi.nlm.nih.gov/pubmed/34711846
http://dx.doi.org/10.1038/s41541-021-00393-6
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