Hammad A, Mossad Y M, Nasef N, Eid R
1 Pediatric Nephrology Unit, Department of Pediatrics, Faculty of Medicine, Mansoura University, Egypt.
2 Clinical Immunology Unit, Clinical Pathology Department & Mansoura Research Centre for Cord Stem Cells (MARC_CSC), Mansoura University, Egypt.
Lupus. 2017 Jul;26(8):871-880. doi: 10.1177/0961203316686845. Epub 2017 Jan 6.
Background Increased expression of interferon-inducible genes is implicated in the pathogenesis of systemic lupus erythematosus (SLE). Interferon regulatory factor 5 (IRF5) is one of the transcription factors regulating interferon and was proved to be implicated in the pathogenesis of SLE in different populations. Objectives The objective of this study was to investigate the correlation between polymorphisms of the IRF5 gene and SLE susceptibility in a cohort of Egyptian children and to investigate their association with clinico-pathological features, especially lupus nephritis. Subjects and methods Typing of interferon regulatory factor 5 rs10954213, rs2004640 and rs2280714 polymorphisms were done using polymerase chain reaction-restriction fragment length polymorphism for 100 children with SLE and 100 matched healthy controls. Results Children with SLE had more frequent T allele and TT genotype of rs2004640 ( P = 0.003 and 0.024, respectively) compared to controls. Patients with nephritis had more frequent T allele of rs2004640 compared to controls ( P = 0.003). However the allele and genotype frequencies of the three studied polymorphisms did not show any difference in patients with nephritis in comparison to those without nephritis. Haplotype GTA of rs10954213, rs2004640 and rs2280714, respectively, was more frequent in lupus patients in comparison to controls ( p = 0.01) while the haplotype GGG was more frequent in controls than lupus patients ( p = 0.011). Conclusion The rs2004640 T allele and TT genotype and GTA haplotype of rs rs10954213, rs2004640, and rs2280714, respectively, can be considered as risk factors for the development of SLE. The presence of the rs2004640 T allele increases the risk of nephritis development in Egyptian children with SLE.
背景 干扰素诱导基因的表达增加与系统性红斑狼疮(SLE)的发病机制有关。干扰素调节因子5(IRF5)是调节干扰素的转录因子之一,已被证明在不同人群的SLE发病机制中起作用。目的 本研究的目的是调查埃及儿童队列中IRF5基因多态性与SLE易感性之间的相关性,并研究它们与临床病理特征尤其是狼疮性肾炎的关联。对象与方法 采用聚合酶链反应-限制性片段长度多态性方法对100例SLE儿童和100例匹配的健康对照进行干扰素调节因子5 rs10954213、rs2004640和rs2280714多态性分型。结果 与对照组相比,SLE儿童rs2004640的T等位基因和TT基因型频率更高(分别为P = 0.003和0.024)。肾炎患者rs2004640的T等位基因频率高于对照组(P = 0.003)。然而,与无肾炎患者相比,三种研究多态性的等位基因和基因型频率在肾炎患者中未显示出任何差异。rs10954213、rs2004640和rs2280714的单倍型GTA在狼疮患者中比对照组更常见(p = 0.01),而单倍型GGG在对照组中比狼疮患者更常见(p = 0.011)。结论 rs2004640的T等位基因和TT基因型以及rs10954213、rs2004640和rs2280714的GTA单倍型可分别被视为SLE发病的危险因素。rs2004640的T等位基因的存在增加了埃及SLE儿童发生肾炎的风险。