嵌合抗原受体
癌症研究
效力
抗原
白血病
免疫学
癌细胞
体外
癌症
生物
免疫疗法
医学
免疫系统
内科学
生物化学
作者
Biao Xi,Robert Berahovich,Hua Zhou,Shuning Xu,Yuehua Wei,Jasper Guan,Hizkia Harto,Jian Guan,Lijun Wu,David Santa Ana,Fabio Cerignoil,Brandon J. Lamarche,Yama Abassi,Vita Golubovskaya
摘要
Chimeric antigen receptor (CAR) T-cell therapy for cancer has achieved significant clinical benefit for resistant and refractory hematological malignancies such as childhood acute lymphocytic leukemia. Efforts are currently underway to extend this promising therapy to solid tumors in addition to other hematological cancers. Here, we describe the development and production of potent CAR T cells targeting antigens with unique or preferential expression on solid and liquid tumor cells. The in vitro potency of these CAR T cells is then evaluated in real-time using the highly sensitive impedance-based xCELLigence assay. Specifically, the impact of different costimulatory signaling domains, such as glucocorticoid-induced tumor necrosis factor receptor (TNFR)-related protein (GITR), on the in vitro potency of CAR T cells is examined. This report includes protocols for: generating CAR T cells for preclinical studies using lentiviral gene transduction, expanding CAR T cells, validating CAR expression, and running and analyzing xCELLigence potency assays.
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