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SLE患者外周血调节性T细胞与IL-10、TGF-β_1的检测 被引量:3

Detection of CD4^+CD25^+ regulation T cells and related cytokines in peripheral blood in SLE patients
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摘要 目的:研究SLE患者外周血CD4+CD25+调节性T细胞(regulation T cells,Tr细胞)及相关细胞因子的变化,分析它们在SLE发病机制中的作用。方法:收集SLE患者及健康对照组外周抗凝静脉血,分离纯化T淋巴细胞。PE标记的抗CD4单抗,FITC标记的抗CD25单抗,作双色流式细胞术,分析SLE患者外周血CD4+CD25+调节性T细胞百分率,ELISA法检测调节性T细胞相关细胞因子的表达。结果:SLE患者外周血Tr细胞的数量明显低于正常对照组[(2.83±1.05)%vs(5.07±0.59)%,P<0.05];患者血清中IL-10、TGF-β1的含量均低于正常对照组,差异有显著性[IL-10:(29.48±13.69)pg/ml vs(43.10±14.95)pg/ml;TGF-β1:(170.04±91.58)pg/ml vs.(254.75±130.41)pg/ml,P<0.05]。患者外周血Tr细胞的比例与血清中IL-10、TGF-β1的含量呈正相关(r1=0.53,r2=0.64,P<0.05)。结论:SLE患者外周血存在细胞免疫功能失调,CD4+CD25+调节性T细胞数量与功能状态发生改变,T淋巴细胞耐受机制的破坏可能与SLE的免疫学发病机制有关。 Objective: To investigate the amount of CD4^+CD25^+ regulation T cells and the level of related cytokines in peripheral blood in SLE patients, and analyze the relationships between CD4^+CD25^+ regulation T cells and the immunopathogenesis of SLE. Methods: CD4^+CD25^+ regulation T cells were detected by flow cytometry in peripheral blood. Besides, related cytokines in peripheral blood were assayed by ELISA. Relativity between CD4^+CD25^+ regulation T cells and related cytokine was analyzed. Results: CD4^+CD25^+ regulation T cells were decreased obviously in peripheral blood in SLE patients compared with control group [ (2.83±1.05)% vs (5.07±0.59)% ,P〈0.05 ]. The level of related cytokines was also decreased in SLE groups compared with control groups[IL-10: (29.48±13.69) pg/ml, vs (43.10±14.95)pg/ml; TGF—β1: ( 170.04± 91.58) pg/ml vs (254.75±130:41)pg/ml,P〈0.05 ].There were positive relationships between CD4^+CD25^+ regulation T cells and related cytokine IL-10, TGFβ1 in SLE patients (r1=0.53 ,r2=0.64,P〈0.05). Conclusion: Celluar immunological function disorder is observed in SLE patients, and the abnormal expression of CD4^+CD25^+ T cells and related cytokines in peripheral blood may be involved in SLE immunopathogenesis.
作者 赖仁建
出处 《中国医药导报》 CAS 2007年第10Z期15-17,共3页 China Medical Herald
关键词 系统性红虎狼疮 调节性T细胞 IL—10 TGF-β1 Systemic lupus erythematosus Regulatory T cell IL-10 TGF-β1
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