嵌合抗原受体
肿瘤微环境
渗透(HVAC)
癌症研究
癌细胞
体内
抗原
免疫系统
免疫疗法
生物
免疫学
癌症
肿瘤细胞
材料科学
遗传学
生物技术
复合材料
作者
Shigao Huang,Fuqiang Xing,Yeneng Dai,Zhiming Zhang,Guangyu Zhou,Shuo Yang,Yucheng Liu,Zhen Yuan,Kathy Qian Luo,Tianlei Ying,Dafeng Chu,Tzu‐Ming Liu,Chu‐Xia Deng,Qi Zhao
标识
DOI:10.1016/j.jconrel.2023.09.007
摘要
Chimeric antigen receptor (CAR)-modified natural killer (NK) cells are recognized as promising immunotherapeutic agents for cancer treatment. However, the efficacy and trafficking of CAR-NK cells in solid tumors are hindered by the complex barriers present in the tumor microenvironment (TME). We have developed a novel strategy that utilizes living CAR-NK cells as carriers to deliver anticancer drugs specifically to the tumor site. We also introduce a time-lapse method for evaluating the efficacy and tumor specificity of CAR-NK cells using a two-photon microscope in live mouse models and three-dimensional (3D) tissue slide cultures. Our results demonstrate that CAR-NK cells exhibit enhanced antitumor immunity when combined with photosensitive chemicals in both in vitro and in vivo tumor models. Additionally, we have successfully visualized the trafficking, infiltration, and accumulation of drug-loaded CAR-NK cells in deeply situated TME using non-invasive intravital two-photon microscopy. Our findings highlight that tumor infiltration of CAR-NK cells can be intravitally monitored through the two-photon microscope approach. In conclusion, our study demonstrates the successful integration of CAR-NK cells as drug carriers and paves the way for combined cellular and small-molecule therapies in cancer treatment. Furthermore, our 3D platform offers a valuable tool for assessing the behavior of CAR cells within solid tumors, facilitating the development and optimization of immunotherapeutic strategies with clinical imaging approaches.
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