Chasov Vitaly, Zmievskaya Ekaterina, Ganeeva Irina, Gilyazova Elvina, Davletshin Damir, Khaliulin Marat, Kabwe Emmanuel, Davidyuk Yuriy N, Valiullina Aygul, Rizvanov Albert, Bulatov Emil
Institute of Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia.
Division of Medical and Biological Sciences, Tatarstan Academy of Sciences, 420111 Kazan, Russia.
Antibodies (Basel). 2024 Feb 1;13(1):10. doi: 10.3390/antib13010010.
Systemic autoimmune diseases (SAIDs), such as systemic lupus erythematosus (SLE), systemic sclerosis (SSc) and rheumatoid arthritis (RA), are fully related to the unregulated innate and adaptive immune systems involved in their pathogenesis. They have similar pathogenic characteristics, including the interferon signature, loss of tolerance to self-nuclear antigens, and enhanced tissue damage like necrosis and fibrosis. Glucocorticoids and immunosuppressants, which have limited specificity and are prone to tolerance, are used as the first-line therapy. A plethora of novel immunotherapies have been developed, including monoclonal and bispecific antibodies, and other biological agents to target cellular and soluble factors involved in disease pathogenesis, such as B cells, co-stimulatory molecules, cytokines or their receptors, and signaling molecules. Many of these have shown encouraging results in clinical trials. CAR-T cell therapy is considered the most promising technique for curing autoimmune diseases, with recent successes in the treatment of SLE and SSc. Here, we overview novel therapeutic approaches based on CAR-T cells and antibodies for targeting systemic autoimmune diseases.
系统性自身免疫性疾病(SAIDs),如系统性红斑狼疮(SLE)、系统性硬化症(SSc)和类风湿性关节炎(RA),与参与其发病机制的先天和适应性免疫系统失调密切相关。它们具有相似的致病特征,包括干扰素特征、对自身核抗原的耐受性丧失以及坏死和纤维化等组织损伤加剧。糖皮质激素和免疫抑制剂特异性有限且容易产生耐受性,被用作一线治疗药物。已经开发出大量新型免疫疗法,包括单克隆抗体和双特异性抗体,以及其他针对参与疾病发病机制的细胞和可溶性因子的生物制剂,如B细胞、共刺激分子、细胞因子或其受体以及信号分子。其中许多在临床试验中都显示出令人鼓舞的结果。CAR-T细胞疗法被认为是治疗自身免疫性疾病最有前景的技术,最近在治疗SLE和SSc方面取得了成功。在此,我们概述基于CAR-T细胞和抗体靶向系统性自身免疫性疾病的新型治疗方法。