炎症
免疫系统
类风湿性关节炎
巨噬细胞极化
透明质酸
补体系统
关节炎
癌症研究
材料科学
滑膜关节
下调和上调
医学
自愈水凝胶
巨噬细胞
细胞因子
免疫学
细胞生物学
受体
免疫增强剂
促炎细胞因子
软骨
佐剂
寡核苷酸
纳米棒
潮湿
信号转导
免疫复合物
病态的
化学
激活剂(遗传学)
补体C1q
药理学
作者
Yu Zhang,Yang Wu,Wei Xiong,Yu Chen,Pengzhen Zhuang,Haoran Wang,Diana M. Toivola,Yawei Du,Hongbo Zhang,Wenguo Cui
标识
DOI:10.1002/adma.202518378
摘要
The positive feedback circuit between the complement system and inflammatory immune responses maps the malignant progression of chronic joint inflammation. Prolonged dysregulation of the immune microenvironment in rheumatoid arthritis (RA) further exacerbates sustained complement activation, thereby establishing a vicious cycle. In this study, MMP-9-responsive, injectable micro-nano geneplexes (C5ASO@HAP-CL-TIMP@HMs) are developed for on-demand regulation of complement component C5, aiming to disrupt this pathological circuit. C5 antisense oligonucleotides (C5ASO) are loaded into cationic liposomes, which are subsequently encapsulated within hyaluronic acid microspheres via click chemistry. In vitro, these geneplexes effectively block abnormal C5 activation in RA synoviocytes, restore macrophage polarization balance, reduce pro-inflammatory cytokine levels and immune complex precursor molecules, and upregulate anti-inflammatory mediators. In an adjuvant-induced arthritis rat model, they significantly alleviate joint swelling and cartilage degradation and suppress inflammatory responses, further highlighting the therapeutic potential of geneplexes in dismantling the complement-inflammation circuit. In summary, the development of micro-nano geneplexes capable of precisely disrupting the complement-inflammatory circuit in RA offers a promising new perspective for the targeted treatment of chronic joint inflammation.
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