Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Trends Biotechnol. 2024 Jul;42(7):842-858. doi: 10.1016/j.tibtech.2024.01.006. Epub 2024 Feb 16.
Current treatment options for autoimmune disease (AID) are essentially immunosuppressive, inhibiting the inflammatory cascade, without curing the disease. Therapeutic monoclonal antibodies (mAbs) that target B cells showed efficacy, emphasizing the importance of B lymphocytes in autoimmune pathogenesis. Treatments that eliminate more potently B cells would open a new therapeutic era for AID. Immune cells can now be bioengineered to express constructs that enable them to specifically eradicate pathogenic B lymphocytes. Engineered immune cells (EICs) have shown therapeutic promise in both experimental models and in clinical trials in AID. Next-generation platforms are under development to optimize their specificity and improve safety. The profound and durable B cell depletion achieved reinforces the view that this biotherapeutic option holds promise for treating AID.
目前治疗自身免疫性疾病(AID)的方法主要是免疫抑制,抑制炎症级联反应,但不能治愈疾病。针对 B 细胞的治疗性单克隆抗体(mAbs)显示出疗效,强调了 B 淋巴细胞在自身免疫发病机制中的重要性。更有效地消除 B 细胞的治疗方法将为 AID 开辟一个新的治疗时代。现在可以对免疫细胞进行生物工程改造,使其表达能够特异性清除致病性 B 淋巴细胞的构建体。在实验模型和 AID 的临床试验中,工程化免疫细胞(EIC)已显示出治疗潜力。正在开发下一代平台以优化其特异性并提高安全性。所达到的深刻和持久的 B 细胞耗竭强化了这样一种观点,即这种生物治疗选择有望治疗 AID。