Therapeutic potential of chimeric antigen receptor based therapies in autoimmune diseases

被引:11
|
作者
Su, Manqiqige [1 ]
Zhao, Chongbo [1 ]
Luo, Sushan [1 ]
机构
[1] Fudan Univ, Dept Neurol, Huashan Hosp, 12 Middle Wulumuqi Rd, Shanghai 200040, Peoples R China
基金
中国国家自然科学基金;
关键词
CAR based therapies; Autoimmune diseases; Recognition domain; Target selection; Precision medicine; REGULATORY T-CELLS; NATURAL-KILLER-CELLS; B-CELLS; MYASTHENIA-GRAVIS; TARGETED THERAPY; CHALLENGES; ANTIBODIES; TCR; AUTOANTIBODIES; RECOGNITION;
D O I
10.1016/j.autrev.2021.102931
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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.
引用
收藏
页数:10
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