Injectable Liquid Crystal Formation System for Reshaping Tumor Immunosuppressive Microenvironment to Boost Antitumor Immunity: Postoperative Chemoimmunotherapy

被引:21
作者
Hu, Mei [1 ]
Zhang, Jiao [1 ]
Yu, Yulin [1 ]
Tu, Kun [1 ]
Yang, Ting [1 ]
Wang, Yi [1 ]
Hu, Qian [1 ]
Kong, Li [1 ]
Zhang, Zhiping [1 ,2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Sch Pharm, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Natl Engn Res Ctr Nanomed, Wuhan 430030, Peoples R China
[3] Huazhong Univ Sci & Technol, Hubei Engn Res Ctr Novel Drug Delivery Syst, Wuhan 430030, Peoples R China
基金
中国国家自然科学基金;
关键词
cancer chemoimmunotherapy; in situ vaccine; liquid crystal formation system; postoperative treatment; tumor microenvironment; IMMUNOGENIC CELL-DEATH; CANCER-IMMUNOTHERAPY; CHECKPOINT BLOCKADE; CUBIC PHASE; NANOPARTICLES; CHEMOTHERAPY; DELIVERY; COMBINATION; RECURRENCE; MECHANISMS;
D O I
10.1002/smll.202004905
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Exploring optimal strategies to improve patient outcome postoperatively is still under challenge. Cancer immunotherapy has great potential to prevent the postoperative tumor recurrence and metastasis, which could be further strengthened by re-education of tumor microenvironment (TME). Herein, a local and sustained drug delivery system of liquid crystal formation system (LCFS) co-loaded with doxorubicin (DOX) and resiquimod (R848) (D/R@LCFS) is reported to confer effective chemoimmunotherapy with reduced systematic toxicity. After local administration, D/R@LCFS turns tumor into in situ vaccine via DOX-triggered immunogenic cell death effect accompanied with immunostimulatory effect of R848. Meanwhile, combination treatment of D/R@LCFS facilitates the recruitment of effector CD8(+) T cells and the polarization of myeloid-derived suppressor cells and immunosuppressive type 2-polarized macrophages to tumoricidal antigen-presenting cells, favoring antigen-specific T cell immune response and inducing more immunogenic phenotypes in tumors. The generated in situ vaccine as well as reshaped TME by D/R@LCFS elicited systematic immune response and long term immune-memory effect in combination with immune checkpoint blockade to significantly prevent postoperative B16F10 or 4T1 tumor recurrence and metastasis. Therefore, this combination strategy of spatiotemporal TME modulation is expected to provide a clinical available option for effective postoperative chemoimmunotherapy.
引用
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页数:15
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