嵌合抗原受体
流式细胞术
生物
恶性肿瘤
癌症研究
CD19
白血病
免疫学
细胞
T细胞
免疫系统
遗传学
作者
Nicholas Tokarew,Javier Suárez Gosálvez,Alessia Nottebrock,Daria Briukhovestka,Stefan Endres,Bruno L. Cadilha,Sebastian Kobold
标识
DOI:10.1016/bs.mcb.2021.06.015
摘要
Adoptive T cell therapy (ACT) is a therapeutic approach which employs genetically manipulated autologous T cells to target and eliminate a patient's malignancy. This novel therapeutic approach, when employing a chimeric antigen receptor (CAR) targeting CD19-expressing B cells, has shown remarkable success in treating acute B-cell lymphocytic leukemia. However, blood born malignancies represent only a fraction of cancers which affect patients. Unfortunately, the utilization of ACT to target solid malignancies has only shown marginal success rates. There are many known obstacles which hinder CAR T cell therapy in patients suffering from solid cancer, one notable obstacle is the effective trafficking of CAR T cells to the tumor site. With the rapid advancement of novel approaches and targets which may enhance CAR T cell infiltration into solid tumors, a standardized approach to assess and measure CAR T cell infiltration becomes imperative in order to compare these different approaches across platforms. Here we describe a flow cytometry method which enables the rapid detection and quantification of CAR T cells which have reached and entered the tumor mass following intravenous injection. Competence with single cell preparation and flow cytometry is required for optimal results.
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