Buc M
Bratisl Lek Listy. 2020;121(1):3-7. doi: 10.4149/BLL_2020_001.
Basic characteristic of the immune system is its ability to distinguish self-molecules, cells, tissues and organs from not self, to tolerate self and dispose of not self. Immunosuppressive mechanisms, especially those mediated by regulatory lymphocytes, play a paramount role in the tolerance mechanisms. When there is an abnormal quantity and/or quality of regulatory cells, various autoimmune diseases are induced, e.g. SLE, RA, T1D, IBD, MS, and others.In recent years, a great progress was achieved in the field how to profit from immunosuppressive properties of T regulatory cells (Treg) in the treatment of patients suffering from autoimmune disorders or transplantation rejections. Nowadays, there are possibilities to up-regulate the function of patient's Tregs or supplement their low numbers. We can up-regulate the function of Treg cells in an affected organism by treatment by low dosage of IL-2 or to treat patients by in vitro expanded Treg cells themselves. Induced Tregs are, however, polyspecific, therefore they have been preferentially used for the treatment graft versus host reactions and some autoimmune disorders only. For those autoimmune diseases, where specific autoantigens are known, Treg cells equipped by antigen-specific chimeric T cell receptor (CARs) were introduced for their treatment (Tab. 1, Fig. 2, Ref. 47). Keywords: AIRE, autoimmune diseases, CAR, cytokines, iNKT cells, regulatory B and T cells.
免疫系统的基本特征是其有能力区分自身分子、细胞、组织和器官与非自身物质,耐受自身并清除非自身物质。免疫抑制机制,尤其是那些由调节性淋巴细胞介导的机制,在耐受机制中起着至关重要的作用。当调节性细胞的数量和/或质量出现异常时,就会引发各种自身免疫性疾病,如系统性红斑狼疮(SLE)、类风湿关节炎(RA)、1型糖尿病(T1D)、炎症性肠病(IBD)、多发性硬化症(MS)等。近年来,在如何利用调节性T细胞(Treg)的免疫抑制特性来治疗自身免疫性疾病患者或移植排斥反应方面取得了巨大进展。如今,有多种方法可以上调患者Treg的功能或补充其数量不足。我们可以通过低剂量白细胞介素-2治疗来上调受影响机体中Treg细胞的功能,或者直接用体外扩增的Treg细胞来治疗患者。然而,诱导性Treg具有多特异性,因此它们仅被优先用于治疗移植物抗宿主反应和某些自身免疫性疾病。对于那些已知特定自身抗原的自身免疫性疾病,引入了配备抗原特异性嵌合T细胞受体(CAR)的Treg细胞来进行治疗(表1、图2、参考文献47)。关键词:自身免疫调节因子(AIRE)、自身免疫性疾病、嵌合抗原受体(CAR)、细胞因子、自然杀伤T细胞(iNKT细胞)、调节性B细胞和T细胞