免疫系统
佐剂
免疫增强剂
抗原
材料科学
自愈水凝胶
细胞免疫
体液免疫
免疫学
淋巴结
体外
纳米纤维
淋巴
间隙
免疫
细胞生物学
超分子化学
生物物理学
免疫疗法
生物
化学
获得性免疫系统
抗原提呈细胞
作者
Shengying Zhang,jingjing Zhou,Yifan Liu,Haoyue Zang,zhidong Teng,Shiqi Sun,Huichen Guo
标识
DOI:10.1021/acsami.6c16060
摘要
Manganese ions (Mn2+), which act as agonists of the cGAS-STING pathway, hold considerable promise as vaccine adjuvants. However, free Mn2+ is rapidly cleared after injection, making it difficult to sustain local immune stimulation. In this study, we exploited the coordination between Mn2+ and rhein, a naturally occurring anthraquinone small molecule, to construct a novel injectable Rhe@Mn hydrogel through one-step self-assembly. Within the hydrogel, densely packed supramolecular nanofibers intertwine to form a three-dimensional network, and energy-dispersive X-ray spectroscopy (EDS) confirmed the uniform distribution of Mn along the nanofibers. Rheological testing showed that the Rhe@Mn hydrogel had favorable viscoelasticity and structural stability. In vitro studies, the Rhe@Mn hydrogel retained the STING-agonist activity of Mn2+ and effectively promoted antigen uptake by DCs and their maturation. In vivo, the hydrogel formed an antigen depot at the injection site, enabling sustained antigen release for up to 10 days. It also efficiently recruited immune cells, including DCs and macrophages, thereby establishing a local immune microenvironment enriched in antigen-presenting cells. After a single immunization, the Rhe@Mn hydrogel vaccine increased the abundance of germinal-center B (GC B) cells in lymph nodes by approximately 3.7-fold, significantly enhanced antigen-specific humoral and cellular immune responses, and established durable immune memory. This study provides a facile, functionally integrated platform for adjuvant-antigen co-delivery in subunit vaccines.
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