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

狂犬病病毒 狂犬病 病毒学 中和抗体 接种疫苗 免疫 生物 抗体 鸭胚疫苗 信使核糖核酸 免疫系统 病毒 免疫学 基因 生物化学
作者
Jiawu Wan,Jianmei Yang,Zongmei Wang,Ruizhong Shen,Chengguang Zhang,Yuntao Wu,Ming Zhou,Huanchun Chen,Zhen F. Fu,Haiwei Sun,Yinglei Yi,Haifa Shen,Hangwen Li,Ling Zhao
出处
期刊:Emerging microbes & infections [Taylor & Francis]
卷期号:12 (2) 被引量:18
标识
DOI:10.1080/22221751.2023.2270081
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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