Xu Yufei, Wang Tao
The sixth cadet regiment, Air Force Medical University, Xi'an 710032, China.
Department of Medical Genetics and Developmental Biology, Air Force Medical University, Xi'an 710032, China. *Corresponding author, E-mail:
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2024 Sep;40(9):834-838.
The classic Chimeric Antigen Receptor Macrophage (CAR-M) exerts pro-inflammatory effects to achieve anti-tumor immunity, but by modifying the structure design of CAR, it can acquire anti-inflammatory functions similar to M2, thereby treating inflammatory diseases. Currently, CAR-M therapy targeting M1-type microglial cells can effectively reduce neuroinflammation and be used to treat inflammation-related depression. With ongoing research on the anti-inflammatory effects of CAR-M, CAR-M cell therapy offers a new approach for treating inflammatory-related diseases.
经典的嵌合抗原受体巨噬细胞(CAR-M)发挥促炎作用以实现抗肿瘤免疫,但通过修改CAR的结构设计,它可以获得类似于M2的抗炎功能,从而治疗炎症性疾病。目前,靶向M1型小胶质细胞的CAR-M疗法可以有效减轻神经炎症,并用于治疗炎症相关的抑郁症。随着对CAR-M抗炎作用的不断研究,CAR-M细胞疗法为治疗炎症相关疾病提供了一种新方法。