背景(考古学)
医学
嵌合抗原受体
免疫学
异硫氰酸荧光素
免疫疗法
自身免疫性疾病
免疫系统
抗体
生物信息学
计算生物学
生物
量子力学
荧光
物理
古生物学
作者
Manqiqige Su,Chongbo Zhao,Sushan Luo
标识
DOI:10.1016/j.autrev.2021.102931
摘要
Chimeric antigen receptor (CAR) based therapies have been adopted as an option for treating autoimmune diseases from the field of blood malignancies by targeting immune cells or rebalancing the pro-inflammatory milieu. Important questions still remained about the efficacy and safety regarding the dynamic and complex autoimmune pathological networks. We here reviewed the emerged developments in basic, translational, and clinical studies of the CAR based therapies in a wide spectrum of autoimmune diseases. The primary goal of the study is to provide some future perspectives on how to optimize the performance of CAR based therapies. The fundamental strategy is to engineer the recognition domains in CAR products for precisely targeting the components in the pro-inflammatory milieu. The second strategy is to incorporate multiple CARs in one carrier, or use fluorescein isothiocyanate (FITC)-CAR T cells for enhancing the therapeutic efficacy. In addition, we reviewed the preclinical evidence in disease-specific context. Overall, we aim to attract more attention in the field of developing future precision CAR based therapies to tailor medial decisions in autoimmune diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI