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An mRNA vaccine against rabies provides strong and durable protection in mice
INTRODUCTION: Rabies is a serious public health problem worldwide for which an effective treatment method is lacking but can be prevented by vaccines. Current vaccines are produced in cell or egg cultures, which are both costly and time consuming. METHODS: Here, a non-replicating mRNA vaccine (RV021...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10639119/ https://www.ncbi.nlm.nih.gov/pubmed/37954577 http://dx.doi.org/10.3389/fimmu.2023.1288879 |
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author | Li, Miao Fang, Enyue Wang, Yunpeng Shi, Leitai Li, Jia Peng, Qinhua Li, Xingxing Zhao, Danhua Liu, Xiaohui Liu, Xinyu Liu, Jingjing Xu, Hongshan Wang, Hongyu Huang, Yanqiu Yang, Ren Yue, Guangzhi Suo, Yue Wu, Xiaohong Cao, Shouchun Li, Yuhua |
author_facet | Li, Miao Fang, Enyue Wang, Yunpeng Shi, Leitai Li, Jia Peng, Qinhua Li, Xingxing Zhao, Danhua Liu, Xiaohui Liu, Xinyu Liu, Jingjing Xu, Hongshan Wang, Hongyu Huang, Yanqiu Yang, Ren Yue, Guangzhi Suo, Yue Wu, Xiaohong Cao, Shouchun Li, Yuhua |
author_sort | Li, Miao |
collection | PubMed |
description | INTRODUCTION: Rabies is a serious public health problem worldwide for which an effective treatment method is lacking but can be prevented by vaccines. Current vaccines are produced in cell or egg cultures, which are both costly and time consuming. METHODS: Here, a non-replicating mRNA vaccine (RV021) encoding the rabies virus glycoprotein was developed in vitro, and its immunogenicity and protective efficacy against live virus was evaluated in mice. RESULTS: A two-dose vaccination with 1 μg of RV021 at 7-day intervals induced a protective level of neutralizing antibody that was maintained for at least 260 days. RV021 induced a robust cellular immune response that was significantly superior to that of an inactivated vaccine. Two doses of 1 μg RV021 provided full protection against challenge with CVS of 30~60-fold lethal dose, 50%. Vaccine potency testing (according to the National Institutes of Health) in vivo revealed that the potency of RV021 at 15 μg/dose was 7.5 IU/dose, which is substantially higher than the standard for lot release of rabies vaccines for current human use. CONCLUSION: The mRNA vaccine RV021 induces a strong protective immune response in mice, providing a new and promising strategy for human rabies prevention and control. |
format | Online Article Text |
id | pubmed-10639119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106391192023-11-11 An mRNA vaccine against rabies provides strong and durable protection in mice Li, Miao Fang, Enyue Wang, Yunpeng Shi, Leitai Li, Jia Peng, Qinhua Li, Xingxing Zhao, Danhua Liu, Xiaohui Liu, Xinyu Liu, Jingjing Xu, Hongshan Wang, Hongyu Huang, Yanqiu Yang, Ren Yue, Guangzhi Suo, Yue Wu, Xiaohong Cao, Shouchun Li, Yuhua Front Immunol Immunology INTRODUCTION: Rabies is a serious public health problem worldwide for which an effective treatment method is lacking but can be prevented by vaccines. Current vaccines are produced in cell or egg cultures, which are both costly and time consuming. METHODS: Here, a non-replicating mRNA vaccine (RV021) encoding the rabies virus glycoprotein was developed in vitro, and its immunogenicity and protective efficacy against live virus was evaluated in mice. RESULTS: A two-dose vaccination with 1 μg of RV021 at 7-day intervals induced a protective level of neutralizing antibody that was maintained for at least 260 days. RV021 induced a robust cellular immune response that was significantly superior to that of an inactivated vaccine. Two doses of 1 μg RV021 provided full protection against challenge with CVS of 30~60-fold lethal dose, 50%. Vaccine potency testing (according to the National Institutes of Health) in vivo revealed that the potency of RV021 at 15 μg/dose was 7.5 IU/dose, which is substantially higher than the standard for lot release of rabies vaccines for current human use. CONCLUSION: The mRNA vaccine RV021 induces a strong protective immune response in mice, providing a new and promising strategy for human rabies prevention and control. Frontiers Media S.A. 2023-10-26 /pmc/articles/PMC10639119/ /pubmed/37954577 http://dx.doi.org/10.3389/fimmu.2023.1288879 Text en Copyright © 2023 Li, Fang, Wang, Shi, Li, Peng, Li, Zhao, Liu, Liu, Liu, Xu, Wang, Huang, Yang, Yue, Suo, Wu, Cao and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Li, Miao Fang, Enyue Wang, Yunpeng Shi, Leitai Li, Jia Peng, Qinhua Li, Xingxing Zhao, Danhua Liu, Xiaohui Liu, Xinyu Liu, Jingjing Xu, Hongshan Wang, Hongyu Huang, Yanqiu Yang, Ren Yue, Guangzhi Suo, Yue Wu, Xiaohong Cao, Shouchun Li, Yuhua An mRNA vaccine against rabies provides strong and durable protection in mice |
title | An mRNA vaccine against rabies provides strong and durable protection in mice |
title_full | An mRNA vaccine against rabies provides strong and durable protection in mice |
title_fullStr | An mRNA vaccine against rabies provides strong and durable protection in mice |
title_full_unstemmed | An mRNA vaccine against rabies provides strong and durable protection in mice |
title_short | An mRNA vaccine against rabies provides strong and durable protection in mice |
title_sort | mrna vaccine against rabies provides strong and durable protection in mice |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10639119/ https://www.ncbi.nlm.nih.gov/pubmed/37954577 http://dx.doi.org/10.3389/fimmu.2023.1288879 |
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