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A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine
African swine fever (ASF) is an acute and highly contagious lethal infectious disease in swine that severely threatens the global pig industry. At present, a safe and efficacious vaccine is urgently required to prevent and control the disease. In this study, we evaluated the safety and immunogenicit...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348041/ https://www.ncbi.nlm.nih.gov/pubmed/37401832 http://dx.doi.org/10.1080/22221751.2023.2233643 |
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author | Liu, Wenming Li, Hengchun Liu, Bo Lv, Tianxing Yang, Chenchen Chen, Si Feng, Liqiang Lai, Liangxue Duan, Ziyuan Chen, Xinwen Li, Pingchao Guan, Suhua Chen, Ling |
author_facet | Liu, Wenming Li, Hengchun Liu, Bo Lv, Tianxing Yang, Chenchen Chen, Si Feng, Liqiang Lai, Liangxue Duan, Ziyuan Chen, Xinwen Li, Pingchao Guan, Suhua Chen, Ling |
author_sort | Liu, Wenming |
collection | PubMed |
description | African swine fever (ASF) is an acute and highly contagious lethal infectious disease in swine that severely threatens the global pig industry. At present, a safe and efficacious vaccine is urgently required to prevent and control the disease. In this study, we evaluated the safety and immunogenicity of replication-incompetent type-2 adenoviruses carrying African swine fever virus (ASFV) antigens, namely CP204L (p30), E183L (p54), EP402R (CD2v), B646L (p72), and B602L (p72 chaperone). A vaccine cocktail delivered by simultaneous intramuscular (IM) and intranasal (IN) administration robustly elicited both systemic and mucosal immune responses against AFSV in mice and swine and provided highly effective protection against the circulating ASFV strain in farmed pigs. This multi-antigen cocktail vaccine was well tolerated in the vaccinated animals. No significant interference among antigens was observed. The combined IM and IN vaccination using this adenovirus-vectored antigen cocktail vaccine warrants further evaluation for providing safe and effective protection against ASFV infection and transmission. |
format | Online Article Text |
id | pubmed-10348041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-103480412023-07-15 A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine Liu, Wenming Li, Hengchun Liu, Bo Lv, Tianxing Yang, Chenchen Chen, Si Feng, Liqiang Lai, Liangxue Duan, Ziyuan Chen, Xinwen Li, Pingchao Guan, Suhua Chen, Ling Emerg Microbes Infect Research Article African swine fever (ASF) is an acute and highly contagious lethal infectious disease in swine that severely threatens the global pig industry. At present, a safe and efficacious vaccine is urgently required to prevent and control the disease. In this study, we evaluated the safety and immunogenicity of replication-incompetent type-2 adenoviruses carrying African swine fever virus (ASFV) antigens, namely CP204L (p30), E183L (p54), EP402R (CD2v), B646L (p72), and B602L (p72 chaperone). A vaccine cocktail delivered by simultaneous intramuscular (IM) and intranasal (IN) administration robustly elicited both systemic and mucosal immune responses against AFSV in mice and swine and provided highly effective protection against the circulating ASFV strain in farmed pigs. This multi-antigen cocktail vaccine was well tolerated in the vaccinated animals. No significant interference among antigens was observed. The combined IM and IN vaccination using this adenovirus-vectored antigen cocktail vaccine warrants further evaluation for providing safe and effective protection against ASFV infection and transmission. Taylor & Francis 2023-07-13 /pmc/articles/PMC10348041/ /pubmed/37401832 http://dx.doi.org/10.1080/22221751.2023.2233643 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Research Article Liu, Wenming Li, Hengchun Liu, Bo Lv, Tianxing Yang, Chenchen Chen, Si Feng, Liqiang Lai, Liangxue Duan, Ziyuan Chen, Xinwen Li, Pingchao Guan, Suhua Chen, Ling A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine |
title | A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine |
title_full | A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine |
title_fullStr | A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine |
title_full_unstemmed | A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine |
title_short | A new vaccination regimen using adenovirus-vectored vaccine confers effective protection against African swine fever virus in swine |
title_sort | new vaccination regimen using adenovirus-vectored vaccine confers effective protection against african swine fever virus in swine |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348041/ https://www.ncbi.nlm.nih.gov/pubmed/37401832 http://dx.doi.org/10.1080/22221751.2023.2233643 |
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