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作 者:李慧娟[1] 马向波 袁立平[1] 徐雪阳 刘德林[1] 项丹丹 刘小红 王俊霞[1] LI Huijuan;MA Xiangbo;YUAN Liping;XU Xueyang;LIU Delin;XIANG Dandan;LIU Xiaohong;WANG Junxia(Department of Rheumatology and Immunology,Handan First Hospital,Handan Hebei 056000,China)
机构地区:[1]邯郸市第一医院风湿免疫科,河北邯郸056000
出 处:《临床与病理杂志》2022年第5期1036-1046,共11页Journal of Clinical and Pathological Research
摘 要:目的:系统性红斑狼疮(systemic lupus erythematosus,SLE)是一种临床表现多样、累及多个器官的自身免疫性疾病。本研究试图识别中性粒细胞相关的SLE生物标志物,为SLE的治疗和管理提供潜在的理论依据。方法:使用加权基因共表达网络分析来自基因表达汇编(Gene Expression Omnibus,GEO)数据库的SLE表达数据,并识别与中性粒细胞相关的模块。结果:鉴定出FPR1、SLC2A3、TLR2、TLR4、CXCR1、MMP25、MGAM和KLHL2共8个关键基因。8个关键基因与中性粒细胞高度相关,并且在SLE中的表达显著上调。结论:通过各种分析和验证,8个关键基因是SLE中与中性粒细胞浸润相关的潜在生物标志物,这为SLE免疫治疗提供了潜在的靶点。Objective:Systemic lupus erythematosus(SLE)is an autoimmune disease with a large variety of clinical manifestations and involving many organs.The purpose of this study was to attempt to identify neutrophil-related SLE biomarkers to provide a potential rationale for the treatment and management of SLE.Methods:Weighted gene co-expression network analysis was used to analyze SLE expression data from the Gene Expression Omnibus(GEO)database,and identify modules related to Neutrophils.Results:Eight key genes(FPR1,SLC2A3,TLR2,TLR4,CXCR1,MMP25,MGAM and KLHL2)were identified.Furthermore,8 key genes were highly correlated with neutrophils and were significantly upregulated in SLE.Conclusion:Through various analyses and confirmations,8 key genes are potential biomarkers associated with Neutrophils infiltration in SLE.It also provides a potential target for SLE immunotherapy.
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