自身免疫
免疫学
免疫系统
调节性T细胞
医学
FOXP3型
免疫耐受
临床试验
T细胞
白细胞介素2受体
内科学
作者
Yu Liu,Yiqiu Fu,Rourou Miao,Jiahui Cao,Fan Zhang,Luntao Liu,Lin Mei,Meitong Ou
标识
DOI:10.1002/adfm.202405133
摘要
Abstract Caused by the loss in the tolerance against self‐antigens, autoimmune diseases are chronic disorders that impact millions of individuals annually with significant economic burden. They are triggered by a deficiency in the quantity or function of regulatory T (Treg) cells, which are essential for maintaining self‐tolerance and preventing excessive immune responses. Several clinical trials over the past decade have demonstrated the safety and feasibility of certain Treg cell‐based therapies against autoimmune diseases, inspiring optimism among patients. Studies have indicated that targeted cell pharmaceuticals are significantly promising, offering superior targeting, improved biocompatibility, and prolonged blood circulation. Thus, Treg cell‐based delivery systems are also extensively studied. This review describes the role of Treg cells in the immune system both in homeostasis and in the development of autoimmunity, purification and expansion methods, derived cell pharmaceutical therapies, and the therapeutic potential for autoimmune diseases, beneficial to accelerating the industrialization and clinical translation of formulations based on Treg cells.
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