Department of Immunology, School of Basic Medical, Central South University, Changsha 410083, China.
Int J Mol Sci. 2023 Dec 16;24(24):17545. doi: 10.3390/ijms242417545.
Natural killer (NK) cells and CD8 T cells can clear infected and transformed cells and generate tolerance to themselves, which also prevents autoimmune diseases. Natural killer group 2 member D (NKG2D) is an important activating immune receptor that is expressed on NK cells, CD8 T cells, γδ T cells, and a very small percentage of CD4 T cells. In contrast, the NKG2D ligand (NKG2D-L) is generally not expressed on normal cells but is overexpressed under stress. Thus, the inappropriate expression of NKG2D-L leads to the activation of self-reactive effector cells, which can trigger or exacerbate autoimmunity. In this review, we discuss the role of NKG2D and NKG2D-L in systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), multiple sclerosis (MS), type I diabetes (T1DM), inflammatory bowel disease (IBD), and celiac disease (CeD). The data suggest that NKG2D and NKG2D-L play a pathogenic role in some autoimmune diseases. Therefore, the development of strategies to block the interaction of NKG2D and NKG2D-L may have therapeutic effects in some autoimmune diseases.
自然杀伤 (NK) 细胞和 CD8 T 细胞可以清除感染和转化的细胞,并对自身产生耐受,从而预防自身免疫性疾病。自然杀伤细胞组 2 成员 D (NKG2D) 是一种重要的激活免疫受体,在 NK 细胞、CD8 T 细胞、γδ T 细胞和一小部分 CD4 T 细胞上表达。相比之下,NKG2D 配体 (NKG2D-L) 通常不在正常细胞上表达,但在应激下过度表达。因此,NKG2D-L 的不适当表达会导致自身反应性效应细胞的激活,从而引发或加重自身免疫。在这篇综述中,我们讨论了 NKG2D 和 NKG2D-L 在系统性红斑狼疮 (SLE)、类风湿关节炎 (RA)、多发性硬化症 (MS)、1 型糖尿病 (T1DM)、炎症性肠病 (IBD) 和乳糜泻 (CeD) 中的作用。数据表明,NKG2D 和 NKG2D-L 在一些自身免疫性疾病中发挥致病作用。因此,开发阻断 NKG2D 和 NKG2D-L 相互作用的策略可能对一些自身免疫性疾病具有治疗效果。