纳米载体
免疫系统
抗原
猪圆环病毒
化学
纳米技术
材料科学
药物输送
体内
卵清蛋白
生物相容性
靶向给药
生物物理学
体外
细胞生物学
免疫原性
作者
Yanling Zhuo,Guiying Wu,Yuanyi Yang,Shuang Li,Yan Wang,Xinyu Huang,Wanping Wu,Qizhuang Lv,Yulong He,Lei Yang
标识
DOI:10.1186/s12951-026-04452-9
摘要
Traditional vaccines targeting porcine circovirus type 2 (PCV2) have several limitations, such as low antigen delivery efficiency and inadequate immunogenicity. To address these challenges, this study developed a bionic nanocarrier (Fe₃O₄@MnSiO₃) that synergistically integrates antigen enrichment and immune stimulation functions. Inspired by the hierarchical structure of sunflower pollen, the design constructs composite particles featuring a superparamagnetic Fe₃O₄ core and a mesoporous MnSiO₃ shell, allowing efficient loading and delivery of the PCV2 Cap protein. Owing to its sophisticated biomimetic architecture, the Fe₃O₄@MnSiO₃ particles exhibit a uniform size, porous structure, and excellent biocompatibility. The Fe₃O₄ core facilitates rapid antigen separation and enrichment, while the porous MnSiO₃ shell provides high antigen loading capacity. This composite structure is efficiently internalized by antigen-presenting cells, enabling controlled antigen release within the intracellular microenvironment. Fe₃O₄@MnSiO₃ exhibits outstanding biocompatibility and release performance in vivo, effectively activating immune responses and enhancing immune stimulation through Mn²⁺ release. In vitro and in vivo studies confirm the superior antigen delivery efficiency and immune activation capacity of this nanocarrier system. Collectively, these properties indicate that the engineered Fe₃O₄@MnSiO₃ multifunctional nanocarrier system functions as an effective vehicle for antigen enrichment and delivery, representing a promising therapeutic strategy for control of PCV2 and related diseases.
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