NKG2D公司
嵌合抗原受体
癌症研究
电穿孔
腹水
结直肠癌
生物
癌细胞
医学
免疫疗法
细胞毒性T细胞
白细胞介素12
癌症
病理
体外
内科学
基因
生物化学
作者
Lin Xiao,Dongzhi Cen,Haining Gan,Yan Sun,Nanqi Huang,Hanzhen Xiong,Qiongmei Jin,Liqun Su,Xuejuan Liu,Kejian Wang,Guang‐Rong Yan,Tianfa Dong,Shangbiao Wu,Pengzhi Zhou,Jinshan Zhang,Weixiang Liang,Junlan Ren,Yaoshu Teng,Can Chen,Xuehu Xu
标识
DOI:10.1016/j.ymthe.2019.03.011
摘要
By fusing the extracellular domain of the natural killer (NK) cell receptor NKG2D to DAP12, we constructed a chimeric antigen receptor (CAR) to improve NK cell tumor responses. An RNA electroporation approach that provides transient expression of the CAR was adopted as a risk mitigation strategy. Expression of the NKG2D RNA CAR significantly augmented the cytolytic activity of NK cells against several solid tumor cell lines in vitro and provided a clear therapeutic benefit to mice with established solid tumors. Three patients with metastatic colorectal cancer were then treated with local infusion of the CAR-NK cells. Reduction of ascites generation and a marked decrease in number of tumor cells in ascites samples were observed in the first two patients treated with intraperitoneal infusion of low doses of the CAR-NK cells. The third patient with metastatic tumor sites in the liver was treated with ultrasound-guided percutaneous injection, followed by intraperitoneal infusion of the CAR-NK cells. Rapid tumor regression in the liver region was observed with Doppler ultrasound imaging and complete metabolic response in the treated liver lesions was confirmed by positron emission tomography (PET)- computed tomographic (CT) scanning. Our results highlight a promising therapeutic potential of using RNA CAR-modified NK cells to treat metastatic colorectal cancer.
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