嵌合抗原受体
生物
免疫疗法
抗原
癌症免疫疗法
CD19
癌症研究
计算生物学
转导(生物物理学)
免疫学
免疫系统
生物化学
作者
Mansour Poorebrahim,Isaac Quiros‐Fernandez,Elham Fakhr,Ángel Cid-Arregui
标识
DOI:10.1016/bs.mcb.2021.07.001
摘要
Cancer immunotherapy is nowadays largely focused on the development of therapeutic antibodies and chimeric antigen receptors (CARs). Two CARs targeting CD19 have been approved recently for the treatment of some hematological malignancies. This demonstrates the capability of engineered CAR T cells in generating effective tumor responses. Furthermore, several hundred ongoing clinical trials are exploring the feasibility of CAR-based approaches to target tumor-associated antigens in solid tumors. However, there still remain significant challenges and limitations in the design and production of CAR-modified T cells that need to be addressed, such as more effective transduction methods, expression and exhaustion issues, reliable in vitro and in vivo characterization methods, etc. Here we describe current techniques for generating CAR T cells using lentiviral vectors as well as detailed protocols for their functional characterization.
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