封锁
肿瘤微环境
免疫检查点
体内
渗透(HVAC)
免疫系统
药理学
药品
舒尼替尼
癌症研究
化学
体外
医学
CD8型
癌症
免疫疗法
受体
内科学
免疫学
肿瘤细胞
生物
材料科学
生物化学
生物技术
复合材料
作者
Yingping Zeng,Yu Tong,Shufen Zhang,Guangtao Song,Tingting Meng,Hong Yuan,Fuqiang Hu
摘要
Tumor vessel normalization can alleviate hypoxia, reduce the intratumoral infiltration of immunosuppressive cells and increase the intratumoral infiltration of immune effector cells (CD8+ T cells), further reversing the immunosuppressive microenvironment. Here, nanocomplexes (lipo/St@FA-COSA/BMS-202) which can accurately deliver drugs to tumor tissues and release different drugs at different sites with different rates were prepared to combine tumor vessel normalization with immune checkpoint blockade. The results of drug release in vitro showed that in a pH 6.5 release medium, lipo/St@FA-COSA/BMS-202 rapidly released the vascular normalizing drug (sunitinib, St) and slowly released the PD-1/PD-L1-blocking drug (BMS-202). The results of in vivo experiments showed that the rapidly released St normalized tumor vessels and formed an immunosupportive microenvironment which improved the anti-tumor efficacy of BMS-202. In conclusion, the drug delivery strategy significantly inhibited tumor growth and had excellent anti-tumor efficacy, which can provide a potential approach for effective tumor treatment.
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