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Fas、FasL在特发性血小板减少性紫癜患者T细胞亚群表达的研究
引用本文:陈婷,彭少华. Fas、FasL在特发性血小板减少性紫癜患者T细胞亚群表达的研究[J]. 咸宁医学院学报, 2009, 23(4): 290-293
作者姓名:陈婷  彭少华
作者单位:咸宁学院附属第一医院内科,湖北,咸宁,437100 
摘    要:目的探讨Fas、FasL在特发性血小板减少性紫癜(rrP)患者T细胞亚群及血小板中的表达状况及其在ITP发病机制中的作用。方法收集ITP患者及健康人群外周抗凝静脉血,分离纯化得T细胞和血小板。以PE标记的anti-CRTH2mAb和cy5标记的anti-CD4、CD8mAb及FTTC标记的anti-Fas、FasL mAb做三色流式细胞术,分析ITP患者Th/Tc、Th1/Th2、Tc1/Tc2细胞Fas、FasL表达的变化;以FITC标记的anti-Fas、FasL mAb作单色流式细胞术,分析ITP患者血小板Fas、FasL表达的变化。结果与健康人群相比,ITP患者外周血Th、Th1、Th2细胞百分率均明显下降(P〈0.05),Tc、Tc1、Tc2细胞百分率均无明显变化(P〉0.05);Th、Th1、Th2及Tc、Tc1、Tc2细胞Fas、FasL表达均明显升高(P〈0.05);同时,111P患者血小板Fas的表达明显升高(P〈0.05),而FasL的表达无明显变化(P〉0.05)。结论ITP患者存在免疫功能失调,T细胞亚群及血小板Fas、FasL表达异常可能与ITP患者免疫病理机制有关。

关 键 词:特发性血小板减少性紫癜  Fas/FasL  T细胞亚群  血小板

Expression of Fas, FasL on T Cell Subsets in Patients with Idiopathic Thrombocytopenic Purpura
CHEN Ting,PENG Shao-hua. Expression of Fas, FasL on T Cell Subsets in Patients with Idiopathic Thrombocytopenic Purpura[J]. Journal of Xianning Medical College, 2009, 23(4): 290-293
Authors:CHEN Ting  PENG Shao-hua
Affiliation:(Department of Internal Medicine, the First Affiliated Hospital of Xianning University ,Xianning Hubei 437100, China)
Abstract:Objective To investigated the expression of Fas, FasL on T cell subsets and thrombocyte in Fas, FasL on T cell subsets was detected by immunofluorescence staining and three-color flow cytometry by Fas/CD4, FasL/CD4, Fas/CD8 and FasL/CD8 gating. The expression of Fas, FasL on thrombocytes was metried by immunofluorescence staining and mono-color flow cytometry by Fas and FasL gating. Results Compared with healthy people, the percentage of Th, Thl and Th2 cells in peripheral blood of ITP patients was markedly decreased, and the expression of Fas, FasL on Th, Thl, Th2, Tc, Tel and Tc2 was significantly increased(P 〈 0.05 ). Meanwhile, the expression of Fas on thrombocytes was also significantly elevated. Conclusion There is immunofunction disorder in ITP patients. , and the abnormal expression of Fas, FasL on T cell subsets and thrombocytes may involve in ITP immunopathogenesis.
Keywords:Fas/FasL
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