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嵌合抗原受体细胞疗法:一种将癌症治疗转变为自身免疫性疾病治疗的革命性方法。

Chimeric antigen receptor cell therapy: A revolutionary approach transforming cancer treatment to autoimmune disease therapy.

作者信息

Wen Ruifan, Li Binbin, Wu Feifeng, Mao Jueyi, Azad Tasnim, Wang Yang, Zhu Junquan, Zhou Xin, Xie Haotian, Qiu Xinying, Hun Marady, Tian Jidong, Zhang Liang, Hong Kimsor, Wen Chuan

机构信息

Medical School, Hunan University of Chinese Medicine, Changsha, China.

Department of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.

出版信息

Autoimmun Rev. 2025 Jun 23;24(9):103859. doi: 10.1016/j.autrev.2025.103859.

Abstract

Currently, autoimmune disorders are predominantly managed with broad-spectrum immunosuppressive agents and monoclonal antibodies, which can alleviate disease symptoms but are rarely curative and are frequently associated with significant adverse effects. Autoreactive B cells play a key role in the pathogenesis of many autoimmune diseases; however, B-cell-depleting therapies such as rituximab have shown limited efficacy in certain autoimmune diseases, primarily due to the persistence of autoreactive B cells within lymphoid tissues and sites of inflammation. Consequently, there is an urgent need for more effective and targeted therapies for patients with severe and refractory autoimmune conditions. In this context, recent advancements in genetic engineering have facilitated the application of cell-based therapies, which have transitioned from oncology to treating autoimmune diseases. Therapies utilizing chimeric antigen receptor (CAR) engineered immune cells have emerged as a promising and potentially curative approach. Clinical trials targeting CD19-expressing B cells in B cell-driven autoimmune diseases, such as systemic lupus erythematosus (SLE), have yielded encouraging results, demonstrating durable remissions in otherwise treatment-resistant cases. In addition, novel strategies are being developed to broaden the therapeutic scope of CAR-based therapies in autoimmunity, including chimeric autoantibody receptor (CAAR)-T cells designed to eliminate autoantigen-specific B cells selectively and CAR-engineered regulatory T cells (CAR-Tregs) aimed at achieving antigen-specific immune modulation and restoration of self-tolerance. Despite these advances, several challenges persist, including short and long-term safety concerns, limited in vivo persistence, and the high costs associated with personalized cell manufacturing. Innovations in CAR design, such as logic-gated CARs, inducible suicide switches, and universal CAR constructs, are under active investigation to enhance safety, control, scalability, and clinical accessibility.

摘要

目前,自身免疫性疾病主要通过广谱免疫抑制剂和单克隆抗体进行治疗,这些药物可以缓解疾病症状,但很少能治愈,且常常伴有显著的副作用。自身反应性B细胞在许多自身免疫性疾病的发病机制中起关键作用;然而,诸如利妥昔单抗等耗竭B细胞的疗法在某些自身免疫性疾病中显示出有限的疗效,主要原因是自身反应性B细胞在淋巴组织和炎症部位持续存在。因此,迫切需要为患有严重和难治性自身免疫性疾病的患者开发更有效、更具针对性的疗法。在这种背景下,基因工程的最新进展促进了基于细胞的疗法的应用,这些疗法已从肿瘤学领域转向治疗自身免疫性疾病。利用嵌合抗原受体(CAR)工程化免疫细胞的疗法已成为一种有前景且可能治愈的方法。针对B细胞驱动的自身免疫性疾病(如系统性红斑狼疮(SLE))中表达CD19的B细胞进行的临床试验取得了令人鼓舞的结果,在原本对治疗耐药的病例中实现了持久缓解。此外,正在开发新的策略以扩大基于CAR的疗法在自身免疫性疾病中的治疗范围,包括旨在选择性消除自身抗原特异性B细胞的嵌合自身抗体受体(CAAR)-T细胞,以及旨在实现抗原特异性免疫调节和恢复自身耐受性的CAR工程化调节性T细胞(CAR-Tregs)。尽管取得了这些进展,但仍存在一些挑战,包括短期和长期安全性问题、体内持久性有限以及与个性化细胞制造相关的高成本问题。目前正在积极研究CAR设计方面的创新技术,如逻辑门控CARs、诱导性自杀开关和通用CAR构建体,以提高安全性、可控性、可扩展性和临床可及性。

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