嵌合抗原受体
生物
背景(考古学)
T细胞
细胞生物学
抗原
T细胞受体
细胞毒性T细胞
免疫学
癌症研究
癌细胞
癌症
免疫系统
体外
遗传学
古生物学
作者
Clara Helena Klee,Alicia Villatoro,Nicholas Casey,Else Marit Inderberg,Sébastien Wälchli
标识
DOI:10.1016/bs.mcb.2023.06.003
摘要
Chimeric antigen receptor (CAR) T cells (CAR T) have emerged as a potential therapy for cancer patients. CAR T cells are capable of recognizing membrane proteins on cancer cells which initiates a downstream signaling in T cells that ends in cancer cell death. Continuous antigen exposure over time, activation of inhibitory signaling pathways and/or chronic inflammation can lead to CAR T cell exhaustion. In this context, the design of CARs can have a great impact on the functionality of CAR T cells, on their potency and exhaustion. Here, using CD19CAR as model, we provide a re-challenge protocol where CAR T cells are cultured weekly with malignant lymphoid cell lines BL-41 and Nalm-6 to simulate them with continuous antigen pressure over a four-week period. This protocol can be value for assessing CAR T cell functionality and for the comparison of different CAR constructs.
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