A tailored nanocarrier DMON and CpGs synergistically drive the formulation of a highly immunogenic and long-acting vaccine against echinococcosis
文献类型: 外文期刊
作者: Ting Xin;Xintao Gao;Siyi Tao;Chenghao Zhou;Zhifang Zhang;Jiabo Ding;Jiaxi Ru;Yinü Li
作者机构:
关键词: CpG adjuvants;DMON nanoparticle;Early, robust and long-lasting immunity;Echinococcosis;Nanocarrier;Vaccine
期刊名称: Materials Today Bio
ISSN: 2590-0064
年卷期: 2025 年 32 卷
页码:
收录情况: SCIE(2025版) ; ; EI(2025版)
摘要: Hydatid disease (echinococcosis) is a zoonotic parasitic disease that seriously endangers human health and livestock production. To develop a safer, more effective vaccine with an exceptionally long-lasting immune response, we employed an ‘all-in-one’ strategy to construct a nanovaccine against echinococcosis. In this system, a dendritic mesoporous organosilica nanoparticle (DMON), Eg95 antigen, and two types of CpG potentiators (CpG ODN and pCpG) were integrated into a single nanoplatform. Compared to the commercial Quil-A-formulated vaccine, these two nanovaccines exhibited significant advantages in inducing early, robust, and long-lasting protective immune responses, especially in terms of IgG1 antibody responses and Th1 cytokine TNF-α secretion. Notably, the certain adjuvant combination (DMON + pCpG) formulated-vaccine Eg95N + pCpG@DMON conferred stronger adjuvanticity to the antigen than Quil-A during the late stage (42–84 days). Systematic evaluation demonstrated excellent biodegradability and biosafety of DMON and its-based vaccine. This research provides a strong foundation for upgrading vaccines against echinococcosis.
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