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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Published in | Frontiers in immunology Vol. 14; p. 1288879 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
26.10.2023
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Subjects | |
Online Access | Get full text |
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Summary: | 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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors have contributed equally to this work Reviewed by: Paulo J. G. Bettencourt, Catholic University of Portugal, Portugal; Sunil Gairola, Serum Institute of India, India Edited by: Dan Peer, Tel Aviv University, Israel |
ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2023.1288879 |