Zhang Qing, Wu Ruifang, Tan Yixin, Huang Junke, Luo Shuaihantian
Department of Dermatology, Hunan Key Laboratory of Medical Epigenomics, The Second Xiangya Hospital of Central South University, Changsha, China.
Department of Dermatology, Hunan Key Laboratory of Medical Epigenomics, The Second Xiangya Hospital of Central South University, Changsha, China.
Int Immunopharmacol. 2023 Apr;117:109979. doi: 10.1016/j.intimp.2023.109979. Epub 2023 Mar 7.
Interferon-inducible 44 like (IFI44L) is a newly discovered gene which has been reported to associate with the susceptibility of some infectious diseases, but there is no data on IFI44L SNP polymorphism associated with Systemic lupus erythematosus (SLE). In this study, we aimed to evaluate the association of IFI44L rs273259 polymorphism with the susceptibility and clinical characteristics of SLE in a Chinese population.
576 SLE patients and 600 controls were recruited in this case-control study. Blood DNA was extracted and IFI44L rs273259 polymorphism was detected by TaqMan SNP Genotyping Assay Kit. The expression levels of IFI44L in Peripheral blood mononuclear cells were detected by RT-qPCR. The DNA methylation levels of IFI44L promoter were detected by bisulfite pyrosequencing.
The genotype and allele frequencies of IFI44L rs273259 in SLE patients have a significantly difference compared to healthy controls (P < 0.001). The genotype AG (vs. AA: OR = 2.849; P < 0.001) and the allele G (vs. A: OR = 1.454; P < 0.001) were associated with increased susceptibility of SLE. IFI44L rs273259 polymorphism was associated with clinical characteristics of SLE including malar rash (P < 0.001), discoid rash (P < 0.001), lupus nephritis (P < 0.001) and anti-Smith antibodies (P < 0.001). The expression levels of IFI44L were most significantly increased in genotype AG than genotype AA and GG (P < 0.01). The DNA methylation levels of IFI44L promoter were most significantly decreased in genotype AG than genotype AA and GG (P < 0.01).
Our results indicate novel polymorphism of IFI44L rs273259 was associated with the susceptibility and clinical characteristics of SLE in the Chinese population.
干扰素诱导44样蛋白(IFI44L)是一个新发现的基因,据报道它与某些传染病的易感性有关,但尚无关于IFI44L单核苷酸多态性(SNP)与系统性红斑狼疮(SLE)相关性的数据。在本研究中,我们旨在评估IFI44L rs273259多态性与中国人群SLE易感性及临床特征的相关性。
本病例对照研究纳入了576例SLE患者和600例对照。提取血液DNA,采用TaqMan SNP基因分型检测试剂盒检测IFI44L rs273259多态性。通过逆转录定量聚合酶链反应(RT-qPCR)检测外周血单个核细胞中IFI44L的表达水平。采用亚硫酸氢盐焦磷酸测序法检测IFI44L启动子的DNA甲基化水平。
与健康对照相比,SLE患者中IFI44L rs273259的基因型和等位基因频率有显著差异(P < 0.001)。基因型AG(与AA相比:比值比[OR] = 2.849;P < 0.001)和等位基因G(与A相比:OR = 1.454;P < 0.001)与SLE易感性增加相关。IFI44L rs273259多态性与SLE的临床特征相关,包括颧部红斑(P < 0.001)、盘状红斑(P < 0.001)、狼疮性肾炎(P < 0.001)和抗史密斯抗体(P < 0.001)。基因型AG中IFI44L的表达水平比基因型AA和GG显著升高(P < 0.01)。基因型AG中IFI44L启动子的DNA甲基化水平比基因型AA和GG显著降低(P < 0.01)。
我们的结果表明,IFI44L rs273259的新型多态性与中国人群SLE的易感性及临床特征相关。