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A two-dose optimum for recombinant S1 protein-based COVID-19 vaccination
BACKGROUND: Recombinant protein subunit vaccination is considered to be a safe, fast and reliable technique when combating emerging and re-emerging diseases such as coronavirus disease 2019 (COVID-19). Typically, such subunit vaccines require the addition of adjuvants to attain adequate immunogenici...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634073/ https://www.ncbi.nlm.nih.gov/pubmed/34864488 http://dx.doi.org/10.1016/j.virol.2021.11.011 |
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author | Hu, Zhidong Chen, Jian-Ping Xu, Jin-Chuan Chen, Zhen-Yan Qu, Rong Zhang, Ling Yao, Wenrong Wu, Juan Yang, Heng Lowrie, Douglas B. Liu, Yong Fan, Xiao-Yong |
author_facet | Hu, Zhidong Chen, Jian-Ping Xu, Jin-Chuan Chen, Zhen-Yan Qu, Rong Zhang, Ling Yao, Wenrong Wu, Juan Yang, Heng Lowrie, Douglas B. Liu, Yong Fan, Xiao-Yong |
author_sort | Hu, Zhidong |
collection | PubMed |
description | BACKGROUND: Recombinant protein subunit vaccination is considered to be a safe, fast and reliable technique when combating emerging and re-emerging diseases such as coronavirus disease 2019 (COVID-19). Typically, such subunit vaccines require the addition of adjuvants to attain adequate immunogenicity. AS01, which contains adjuvants MPL and saponin QS21, is a liposome-based vaccine adjuvant system that is one of the leading candidates. However, the adjuvant effect of AS01 in COVID-19 vaccines is not well described yet. METHODS: In this study, we utilized a mixture of AS01 as the adjuvant for an S1 protein-based COVID-19 vaccine. RESULTS: The adjuvanted vaccine induced robust immunoglobulin G (IgG) binding antibody and virus-neutralizing antibody responses. Importantly, two doses induced similar levels of IgG binding antibody and neutralizing antibody responses compared with three doses and the antibody responses weakened only slightly over time up to six weeks after immunization. CONCLUSION: These results suggested that two doses may be enough for a clinical vaccine strategy design using MPL & QS21 adjuvanted recombinant protein, especially in consideration of the limited production capacity of COVID-19 vaccine in a public health emergency. |
format | Online Article Text |
id | pubmed-8634073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86340732021-12-01 A two-dose optimum for recombinant S1 protein-based COVID-19 vaccination Hu, Zhidong Chen, Jian-Ping Xu, Jin-Chuan Chen, Zhen-Yan Qu, Rong Zhang, Ling Yao, Wenrong Wu, Juan Yang, Heng Lowrie, Douglas B. Liu, Yong Fan, Xiao-Yong Virology Article BACKGROUND: Recombinant protein subunit vaccination is considered to be a safe, fast and reliable technique when combating emerging and re-emerging diseases such as coronavirus disease 2019 (COVID-19). Typically, such subunit vaccines require the addition of adjuvants to attain adequate immunogenicity. AS01, which contains adjuvants MPL and saponin QS21, is a liposome-based vaccine adjuvant system that is one of the leading candidates. However, the adjuvant effect of AS01 in COVID-19 vaccines is not well described yet. METHODS: In this study, we utilized a mixture of AS01 as the adjuvant for an S1 protein-based COVID-19 vaccine. RESULTS: The adjuvanted vaccine induced robust immunoglobulin G (IgG) binding antibody and virus-neutralizing antibody responses. Importantly, two doses induced similar levels of IgG binding antibody and neutralizing antibody responses compared with three doses and the antibody responses weakened only slightly over time up to six weeks after immunization. CONCLUSION: These results suggested that two doses may be enough for a clinical vaccine strategy design using MPL & QS21 adjuvanted recombinant protein, especially in consideration of the limited production capacity of COVID-19 vaccine in a public health emergency. Published by Elsevier Inc. 2022-01 2021-12-01 /pmc/articles/PMC8634073/ /pubmed/34864488 http://dx.doi.org/10.1016/j.virol.2021.11.011 Text en © 2021 Published by Elsevier Inc. 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 Hu, Zhidong Chen, Jian-Ping Xu, Jin-Chuan Chen, Zhen-Yan Qu, Rong Zhang, Ling Yao, Wenrong Wu, Juan Yang, Heng Lowrie, Douglas B. Liu, Yong Fan, Xiao-Yong A two-dose optimum for recombinant S1 protein-based COVID-19 vaccination |
title | A two-dose optimum for recombinant S1 protein-based COVID-19 vaccination |
title_full | A two-dose optimum for recombinant S1 protein-based COVID-19 vaccination |
title_fullStr | A two-dose optimum for recombinant S1 protein-based COVID-19 vaccination |
title_full_unstemmed | A two-dose optimum for recombinant S1 protein-based COVID-19 vaccination |
title_short | A two-dose optimum for recombinant S1 protein-based COVID-19 vaccination |
title_sort | two-dose optimum for recombinant s1 protein-based covid-19 vaccination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634073/ https://www.ncbi.nlm.nih.gov/pubmed/34864488 http://dx.doi.org/10.1016/j.virol.2021.11.011 |
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