A single immunization with core-shell structured lipopolyplex mRNA vaccine against rabies induces potent humoral immunity in mice and dogs

被引:18
作者
Wan, Jiawu [1 ,2 ,3 ,4 ]
Yang, Jianmei [5 ]
Wang, Zongmei [1 ,2 ,3 ,4 ]
Shen, Ruizhong [5 ]
Zhang, Chengguang [1 ,2 ,3 ,4 ]
Wu, Yuntao [5 ]
Zhou, Ming [1 ,2 ,3 ,4 ]
Chen, Huanchun [1 ,2 ,3 ,4 ]
Fu, Zhen F. [1 ,2 ,3 ,4 ]
Sun, Haiwei [5 ]
Yi, Yinglei [5 ]
Shen, Haifa [5 ]
Li, Hangwen [5 ]
Zhao, Ling [1 ,2 ,3 ,4 ]
机构
[1] Huazhong Agr Univ, State Key Lab Agr Microbiol, Wuhan, Peoples R China
[2] Huazhong Agr Univ, Coll Vet Med, Key Lab Prevent Vet Med Hubei Prov, Wuhan, Peoples R China
[3] Hubei Hongshan Lab, Wuhan, Peoples R China
[4] Frontiers Sci Ctr Anim Breeding & Sustainable Prod, Wuhan, Peoples R China
[5] Stemirna Therapeut, Shanghai, Peoples R China
关键词
RABV; Lipopolyplex; mRNA vaccine; humoral immunity; dogs; LIPID NANOPARTICLES; PROTEIN EXPRESSION; GLOBAL RABIES; IMMUNOGENICITY; PSEUDOURIDINE; VIRUS;
D O I
10.1080/22221751.2023.2270081
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The persistence and clinical consequences of rabies virus (RABV) infection have prompted global efforts to develop a safe and effective vaccines against rabies. mRNA vaccines represent a promising option against emerging and re-emerging infectious diseases, gaining particular interest since the outbreak of COVID-19. Herein, we report the development of a highly efficacious rabies mRNA vaccine composed of sequence-modified mRNA encoding RABV glycoprotein (RABV-G) packaged in core-shell structured lipopolyplex (LPP) nanoparticles, named LPP-mRNA-G. The bilayer structure of LPP improves protection and delivery of RABV-G mRNA and allows gradual release of mRNA molecules as the polymer degrades. The unique core-shell structured nanoparticle of LPP-mRNA-G facilitates vaccine uptake and demonstrates a desirable biodistribution pattern with low liver targeting upon intramuscular immunization. Single administration of low-dose LPP-mRNA-G in mice elicited potent humoral immune response and provided complete protection against intracerebral challenge with lethal RABV. Similarly, single immunization of low-dose LPP-mRNA-G induced high levels of virus-neutralizing antibody titers in dogs. Collectively, our data demonstrate the potential of LPP-mRNA-G as a promising next-generation rabies vaccine used in human and companion animals.
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页数:17
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