间充质干细胞
类风湿性关节炎
药物输送
脂质体
靶向给药
材料科学
关节炎
药品
干细胞
医学
免疫学
药理学
纳米技术
生物
细胞生物学
病理
作者
Ma Lan,Honghui Wu,Jian Cao,Nan Zhang,Yaosheng Li,Juanjuan Zheng,Xinchi Jiang,Jianqing Gao
标识
DOI:10.1021/acsami.4c09080
摘要
Rheumatoid arthritis (RA) is a systemic autoimmune disorder that severely compromises joint health. The primary therapeutic strategy for advanced RA aims to inhibit joint inflammation. However, the nonspecific distribution of pharmacological agents has limited therapeutic efficacy and heightens the risks associated with RA treatment. To address this issue, we developed mesenchymal stem cell (MSC)-based biomimetic liposomes, termed MSCsome, which were composed of a fusion between MSC membranes and liposomes. MSC some with relatively simple preparation method effectively enhanced the targeting efficiency of drug to diseased joints. Interaction between lymphocyte function-associated antigen-1 and intercellular adhesion molecule-1 enhanced the affinity of the MSCsome for polarized macrophages, thereby improving its targeting capability to affected joints. The effective targeted delivery facilitated drug accumulation in joints, resulting in the significant inhibition of the inflammation, as well as protection and repair of the cartilage. In conclusion, this study introduced MSCsome as a promising approach for the effective treatment of advanced RA, providing a novel perspective on targeted drug delivery therapy for inflammatory diseases.
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