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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
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.
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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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