免疫原性
间充质干细胞
地塞米松
微泡
自身免疫性肝炎
肝损伤
外体
刀豆蛋白A
肝炎
生物相容性
癌症研究
医学
药品
药理学
免疫学
化学
抗原
体外
内科学
生物化学
小RNA
病理
基因
有机化学
作者
Jiawei Zhao,Yue Li,Rongrong Jia,Jinghui Wang,Min Shi,Yugang Wang
标识
DOI:10.3389/fbioe.2021.650376
摘要
Exosomes (Exos) are nanosized vesicles (around 100 nm) that recently serve as a promising drug carrier with high biocompatibility and low immunogenicity. Previous studies showed that Exos secreted from mesenchymal stem cells (MSCs) provide protection for concanavalin A (Con A)-induced liver injury. In this study, the protective effect of Exos is confirmed, and dexamethasone (DEX)-incorporated Exos named Exo@DEX are prepared. It is then investigated whether Exo@DEX can function more efficiently compared to free drugs and naive Exos in a Con A-induced autoimmune hepatitis (AIH) mouse model. The results show that Exo@DEX efficiently improves the accumulation of DEX in AIH in the liver. These data suggest that Exo@DEX is a promising drug carrier for AIH and could have applications in other diseases.
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