Xi Biao, Berahovich Robert, Zhou Hua, Xu Shirley, Wei Yuehua, Guan Jasper, Harto Hizkia, Guan Jian, Wu Lijun, Santa Ana David, Cerignoil Fabio, Lamarche Brandon, Abassi Yama A, Golubovskaya Vita
ACEA Biosciences, Inc;
ProMab Biotechnologies. Inc.
J Vis Exp. 2019 Nov 12(153). doi: 10.3791/59033.
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.
嵌合抗原受体(CAR)T细胞疗法在治疗癌症方面已为耐药和难治性血液系统恶性肿瘤(如儿童急性淋巴细胞白血病)带来了显著的临床益处。目前正在努力将这种前景广阔的疗法扩展至实体瘤以及其他血液系统癌症。在此,我们描述了针对在实体瘤和液体肿瘤细胞上具有独特或优先表达的抗原的强效CAR T细胞的开发和生产过程。然后,使用基于阻抗的高灵敏度xCELLigence检测法实时评估这些CAR T细胞的体外效力。具体而言,研究了不同共刺激信号域,如糖皮质激素诱导的肿瘤坏死因子受体(TNFR)相关蛋白(GITR)对CAR T细胞体外效力的影响。本报告包括以下方案:使用慢病毒基因转导生成用于临床前研究的CAR T细胞、扩增CAR T细胞、验证CAR表达以及进行和分析xCELLigence效力检测。