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Enhancing protective immunity against bacterial infection via coating nano-Rehmannia glutinosa polysaccharide with outer membrane vesicles

文献类型： 外文期刊

作者： Huang, Yee 1 ; Sun, Jiaying 1 ; Cui, Xuemei 1 ; Li, Xuefeng 1 ; Hu, Zizhe 1 ; Ji, Quanan 1 ; Bao, Guolian 1 ; Liu, Yan 1 ;

作者机构： 1.Zhejiang Acad Agr Sci, Inst Anim Husb & Vet Sci, Hangzhou, Zhejiang, Peoples R China

2.China Jiliang Univ, Coll Life Sci, Hangzhou, Zhejiang, Peoples R China

关键词： Bordetella bronchiseptica; dendritic cells; outer membrane vesicle; subunit vaccine; transcriptomic analysis

期刊名称：JOURNAL OF EXTRACELLULAR VESICLES （ 影响因子：14.5； 五年影响因子：16.7 ）

ISSN：

年卷期： 2024 年 13 卷 9 期

页码：

收录情况： SCI

摘要： With the coming of the post-antibiotic era, there is an increasingly urgent need for safe and efficient antibacterial vaccines. Bacterial outer membrane vesicles (OMVs) have received increased attention recently as a potential subunit vaccine. OMVs are non-replicative and contain the principle immunogenic bacterial antigen, which circumvents the safety concerns of live-attenuated vaccines. Here, we developed a novel nano-vaccine by coating OMVs onto PEGylated nano-Rehmannia glutinosa polysaccharide (pRL) in a structure consisting of concentric circles, resulting in a more stable vaccine with improved immunogenicity. The immunological function of the pRL-OMV formulation was evaluated in vivo and in vitro, and the underlying mechanism was studied though transcriptomic analysis. The pRL-OMV formulation significantly increased dendritic cell (DC) proliferation and cytokine secretion. Efficient phagocytosis of the formulation by DCs was accompanied by DC maturation. Further, the formulation demonstrated superior lymph node targeting, contributing to a potent mixed cellular response and bacterial-specific antibody response against Bordetella bronchiseptica infection. Specifically, transcriptomic analysis revealed that the immune protection function correlated with T-cell receptor signalling and Th1/Th2/Th17 differentiation, among other markers of enhanced immunological activity. These findings have implications for the future application of OMV-coated nano-carriers in antimicrobial immunotherapy.

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