Targeted Delivery of Dasatinib to Deplete Tumor-Associated Macrophages by Mannosylated Mixed Micelles for Tumor Immunotherapy

被引:15
|
作者
Zhang, Xiaoxu [1 ]
Zang, Xinlong [2 ]
Qiao, Mingxi [1 ]
Zhao, Xiuli [1 ]
Hu, Haiyang [1 ]
Chen, Dawei [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China
[2] Qingdao Univ, Sch Basic Med, Qingdao 266071, Peoples R China
基金
中国国家自然科学基金;
关键词
tumor-associated macrophages; dasatinib; mixed micelles; tumor microenvironment (TME); tumor immunotherapy; RESISTANCE; GROWTH;
D O I
10.1021/acsbiomaterials.0c01046
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Tumor-associated macrophages (TAMs) are abundant in tumors and predominately show protumor M2-type fostering tumor progression. Specific depletion of TAMs is conceivably favorable for antitumor therapy. In this study, mannosylated mixed micelles (DAS-MMic) were developed to specifically deliver dasatinib (DAS) to eliminate TAMs for tumor immunotherapy. In vitro and in vivo results showed that DAS-MMic could effectively eradicate TAMs, decrease angiogenesis, reprogram the immunosuppressive tumor microenvironment, and finally suppress tumor progression. These data suggest the potential of direct elimination of TAMS by DAS-MMic for tumor immunotherapy.
引用
收藏
页码:5675 / 5684
页数:10
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