期刊文献+

Th17/调节性T细胞在类风湿关节炎中的作用及其意义 被引量:12

The role and significance of Thelper cell subtypes in the pathogenesis of rheumatoid arthritis
原文传递
导出
摘要 目的探讨Thl,Th2,Thl7,调节性T细胞分化及相关细胞因子在类风湿关节炎(RA)发病机制的相关性。方法选取7l例RA患者作为试验对象,并根据DAS28评分,分为高、中、低活动组,采集试验对象及健康对照组(18名)外周血,采用流式细胞术分别检测Thl,Th2,Thl7及调节性T细胞在RA患者不同活动组的百分率。统计学方法采用t检验。结果RA患者外周血Thl[(6.2+4.5)%],Thl7[(1.1±0.9)%],调节性T细胞[(1.8+1.2)%]所占外周细胞比例与健康对照组比较差异有统计学意义(P〈0.05);且Thl,Thl7,调节性T细胞比例与DAS28评分有关。结论Thl,Thl7细胞参与疾病的发生、发展;Th2、调节性T细胞可能阻止疾病的进一步发展。 Objective To explore the correlation between Thl, Th2, Thl7, and Treg cells differentiation and related cytokines in patients with rheumatoid arthritis (RA). Methods Seventy one patients with active RA were enrolled in this study. They were divided into low, moderate and high disease activity groups according to disease activity score (DAS28). The frequencies of Thl, Th2, Thl7, and Treg cells in the peripheral blood of RA patients group (n=71) and healthy control group (n=18) were determined by flow cytometry. T test was used for statistical analysis. Results Significant difference could be detected between the proportions of Thl [(6.2±4.5)%1, Thl7 [(1.1±0.9)%] and Treg [(1.8±1.2)%] cells in the peripheral blood of RA patients and the control group (P〈0.05), and there was correlation between proportions of these three kinds of cell and the DAS28. Conclusion Thl and Th 17 cells may promote the development of RA disease, but Th2 and Treg cells could prevent further development of RA disease.
出处 《中华风湿病学杂志》 CAS CSCD 北大核心 2012年第4期229-232,共4页 Chinese Journal of Rheumatology
基金 山西省自然科学基金(2007011116)
关键词 Th17/调节性T细胞 类风湿关节炎 患病率 治疗 Arthritis, rheumatoid Thl cells Thelper cell subtypes
  • 相关文献

参考文献14

  • 1Jacobson DL,Gange S.J,Rose NR. Epidemiology and estimated population burden of selected autoimmune diseases in the United States[J].Clinical Immunology and Immunopathology,1997.223-243.doi:10.1006/clin.1997.4412.
  • 2严瑾,刘岳凤,张永如.云克联合治疗对类风湿关节炎的临床及实验室指标的影响[J].重庆医科大学学报,2010,35(11):1713-1715. 被引量:22
  • 3Zhu JF,Paul EW. CD4 T cells:fates,functions,and faults[J].Blood,2008.1557-1569.
  • 4Boissier MC,Assier E,Falgaronc G. Shifting the imbalance from Th1/Th2 to Th17/Treg:the changing rheumatoid arthritis paradigm[J].Joint Bone Spine:Revue du Rhumatisme,2008.373-375.
  • 5Harrington LE,Mangan PR,Weaver CT. Expanding the effector CD4 T-cell repertoire:the Th17 lineage[J].Current Opinion in Immunology,2006.349-356.
  • 6Feldmann M,Brennan FM,Maini RN. Rheunatoid arthritis[J].Cell,1996.307-310.doi:10.1016/S0092-8674(00)81109-5.
  • 7Miosace P. Interlcukin-17 in rheumatoid arthritis:if T cells were to contribute to inflammation and destruction through synergy[J].Arthritis and Rheumatism,2003.594-601.
  • 8Raza K,Scheel-Toellner D,Lee CY. Synovial fluid leukocyte apoptosis is inhibited in patients with very early rheumatoid arthritis[J].Arthritis Research & Therapy,2006.120.doi:10.1186/ar2009.
  • 9Sakaguchi S. Regulatory T cells:key controllers of immunologie self-tolerance[J].Cell,2000.455-458.doi:10.1016/S0092-8674(00)80856-9.
  • 10宋琳婕,王嘉军.Treg细胞与类风湿关节炎的最新研究进展[J].中国医药指南,2011,9(21):219-221. 被引量:6

二级参考文献15

共引文献26

同被引文献106

引证文献12

二级引证文献110

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部