Division of Rheumatology and Clinical Immunology, Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Cells. 2021 Apr 21;10(5):964. doi: 10.3390/cells10050964.
Interleukin-18 receptor accessory protein (IL18RAP) is an indispensable subunit for the IL-18 receptor (IL-18R) complex's ability to mediate high-affinity IL-18 binding and signalling transduction. Interest in IL-18 in systemic lupus erythematosus (SLE) has been mostly focused on its role as a type 1 T helper cell-driving cytokine. The functional significance of IL18RAP in mediating the IL-18-driven response in myeloid cells in SLE remains largely unexplored. This study aimed to investigate the expression and function significance of IL18RAP in neutrophils of SLE patients. By qRT-PCR and Western blot analyses, elevated expressions of IL18RAP mRNA and protein were observed in neutrophils from SLE patients-particularly those with a history of nephritis. IL18RAP expression correlated negatively with complement 3 level and positively with disease activity, with higher expression in patients exhibiting renal and immunological manifestations. The increased IL18RAP expression in SLE neutrophils could be attributed to elevated type I interferon level in sera. Functionally, neutrophils from SLE patients showed higher IL-18-mediated enhancement in reactive oxygen species (ROS) generation, which showed positive correlation with IL18RAP expression and could be neutralized by anti-IL18RAP blocking antibodies. Taken together, our findings suggest that IL-18 could contribute to SLE pathogenesis through mediation of neutrophil dysfunction via the upregulation of IL18RAP expression.
白细胞介素-18 受体辅助蛋白 (IL18RAP) 是白细胞介素-18 受体 (IL-18R) 复合物介导高亲和力白细胞介素-18 结合和信号转导能力所必需的亚单位。人们对系统性红斑狼疮 (SLE) 中白细胞介素-18 的兴趣主要集中在其作为 1 型辅助性 T 细胞驱动细胞因子的作用上。IL18RAP 在介导 SLE 中髓样细胞中白细胞介素-18 驱动反应中的功能意义在很大程度上尚未得到探索。本研究旨在研究 SLE 患者中性粒细胞中 IL18RAP 的表达和功能意义。通过 qRT-PCR 和 Western blot 分析,观察到 SLE 患者中性粒细胞中 IL18RAP mRNA 和蛋白表达升高,尤其是有肾炎病史的患者。IL18RAP 表达与补体 3 水平呈负相关,与疾病活动呈正相关,在表现出肾脏和免疫表现的患者中表达更高。SLE 中性粒细胞中 IL18RAP 的增加可归因于血清中 I 型干扰素水平升高。功能上,SLE 患者的中性粒细胞显示出更高的白细胞介素-18 介导的活性氧 (ROS) 生成增强,这与 IL18RAP 表达呈正相关,并且可以被抗 IL18RAP 阻断抗体中和。总之,我们的研究结果表明,白细胞介素-18 可能通过上调 IL18RAP 表达介导中性粒细胞功能障碍来促进 SLE 的发病机制。