嵌合抗原受体
免疫学
细胞疗法
免疫系统
自身抗体
抗原
自身免疫
医学
颗粒酶
穿孔素
T细胞
生物
细胞
抗体
CD8型
遗传学
作者
Xiaoxiao Yu,Haodong Shang,Xinru Shen,Jing Zhang,Ting Chang,Zhe Ruan,Yong-liang Jia,Feng Gao
摘要
The conventional clinical therapies for autoimmune diseases (ADs) lack specificity, necessitating long-term medication that can lead to serious side effects. In contrast, chimeric antigen receptor (CAR) T cell therapy for ADs, characterized by fewer side effects and longer-lasting therapeutic effects, represents a new direction for the specific treatment of ADs. T cells modified with CAR genes possess the ability to not only secrete perforin, granzymes, and other molecules that target autoreactive immune cells but also to lead effector and regulatory T cells into autoimmune environments, thereby exerting transport, proliferation, and immune regulatory functions. Chimeric autoantibody receptor T cells can recognize and kill autoreactive cells expressing target autoantibodies through their specific antigens. In this article, we comprehensively expound on the application of CAR-T cell therapy in different ADs and summarize the current research progress in this regard. This review aims to enhance the application of CAR-T therapy in AD treatment and facilitate further studies aimed at addressing the existing gaps in CAR-T therapy for ADs.
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