PUBLICATION

An mRNA vaccine induces antimycobacterial immunity by activating DNA damage repair and autophagy

Authors
Chen, D., Huang, W., Shen, L., Zhang, J., Pan, Z., Zhang, C., Tang, Y., Zhou, Z., Tao, J., Luo, G., Zhang, S., Zhou, J., Xu, S., Zhang, M., Li, Y., Fang, Y., Zhao, F., Huang, L., Li, H., Yang, H., Lv, H., Sha, W., Yan, B., Liu, J., Zhang, L.
ID
ZDB-PUB-250109-164
Date
2024
Source
Molecular therapy. Nucleic acids   36: 102402102402 (Journal)
Registered Authors
Keywords
DNA damage repair, MT: Oligonucleotides: Therapies and Applications, autophagy, granuloma, mRNA vaccine, tuberculosis
Datasets
GEO:GSE269547, GEO:GSE270105
MeSH Terms
none
PubMed
39759874 Full text @ Mol Ther Nucleic Acids
Abstract
Effective vaccines are urgently needed for the control of tuberculosis (TB). Here, we report that an mRNA TB vaccine is highly effective and exhibits both prophylactic and therapeutic activity in the zebrafish model of TB. Adult zebrafish immunized with the mRNA vaccine survived significantly longer after Mycobacterium marinum challenge compared to those immunized with the DNA vaccine. Furthermore, post-infection treatment with the mRNA vaccine drastically reduced the bacterial burden. The mRNA vaccine activated multiple DNA break repair systems that are essential for the normal development and function of adaptive immunity, but did not activate the canonical DNA damage responses that promote cell death. This highlights a profound connection between DNA damage repair and the activation of immune responses under physiological processes of immunization. Remarkably, the mRNA vaccine induced autophagy in granulomas, coinciding with bacterial killing and cell survival. Collectively, these findings demonstrate that the mRNA vaccine elicits potent innate and adaptive immunity, providing effective host protection against mycobacterial challenge.
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