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紫癜性肾炎患儿外周血CD4+CD25+调节性T细胞的临床意义 被引量:5

Significance of CD4+CD25+ Regulation T Cells in Children with Nephritis of Schonlein-Henoch Purpura
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摘要 目的研究紫癜性肾炎(HSPN)患儿外周血CD4+CD25+调节性T细胞数量、相关细胞因子的水平及Foxp3的表达,探讨它们在HSPN发病机制中的作用。方法分别采集40例HSPN患儿及20例健康儿童外周静脉血,通过流式细胞仪分析CD4+CD25+调节性T细胞百分率,ELISA测定血浆IL-10和TGF-61水平,荧光定量PCR(Real—timePCR)检测T细胞Foxp3mRNA的表达。结果HSPN患儿外周血CD4+T,CD25+T,CD4+CD25+T/CD4+T均低于对照组(P〈0.05);T细胞Foxp3mRNA的表达明显降低,血浆IL-10水平也明显低于对照组(P〈0.05),血浆TGF-β1水平较对照组明显升高(P〈0.01);CD4+CD25+调节性T细胞百分率随HSPN病理分级加重有降低趋势,二者呈负相关(r=0.966,P〈0.01)。结论HSPN患儿外周血存在细胞免疫功能失调,CD4+CD25+调节性T细胞数量减少或功能异常,导致免疫抑制效应不足,参与并促进了儿童HSPN的发生发展,其外周血水平与HSPN病理分级有相关性。 Objective To investigate the amount of CD4+CD25+ regulation T cells,the level of related cytokine and the expression of Foxp3 in peripheral blood in children with HSPN ,and explore the correlation of CD4+CD25+ regulation T cells with the pathogenesis of HSPN. Methods 40 patients with HSPN and 20 age-matched healthy children were detected. Flow cytometric analysis(FCM) was performed to detect the percentage of CD4+CD25+ regulation T cells suhpopulation. Enzyme-linked immunosorbent assay(ELISA) was used to measure the levels of related cytokines (IL-10 and TGF-β) and real-time PCR were used to analyse Foxp3 expression. Results Compared with control group,CD4+CD25+ regulation T cells were significantly lower in peripheral blood in HSPN children ,and the expression of Foxp3 mRNA were decreased obviously also (P〈0. 05). IL-10 level was markedly lower and TGF-β1 level was significantly higher in HSPN children. The percentage of CD4+CD25+ regulation T cells correlated negatively with renal pathologic grade in HSPN (r=-0. 966,P〈( 0. 01). Conclusion Cellular immunological function disorder is observed in HSPN children. The decrease or afunction of CD4+CD25+ regulation T cells will participate in and promote the development of HSPN of children. And its percentage correlate with renal pathologic grade in HSPN.
出处 《现代检验医学杂志》 CAS 2011年第1期74-75,78,共3页 Journal of Modern Laboratory Medicine
关键词 紫癜性肾炎 CD4+CD25+调节性T细胞 白细胞介素-10 转化生长因子-β1 FOXP3 henoch-schonlein purpura nephritis CD4+CD25+ regulation T cells IL-10 TGF-β1 Foxp3
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