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机构地区:[1]贵阳医学院附属医院中心实验室,贵阳550004 [2]贵阳医学院附属医院血液内科,贵阳550004
出 处:《中国免疫学杂志》2011年第9期840-843,共4页Chinese Journal of Immunology
基 金:贵州省卫生厅资助项目(G2003-6)
摘 要:目的:探讨Th及NKT细胞内细胞因子(Intracellular cytokine,ICK)在再生障碍性贫血(Aplastic anemia,AA)发病中所起的作用。方法:流式细胞术(FCM)检测Th细胞表面CD3+CD4+分子、NKT细胞表面CD3+CD16+56+分子,细胞内染色技术检测Th、NKT细胞内IFN-γ和IL-4水平。结果:AA患者外周血Th细胞减少(P<0.01),细胞内CD3+CD4+IFN-γ+、CD3+CD4+IL-4+均增高,Th1/Th2增高(P<0.01);NKT细胞增多(P<0.05),NKT细胞内IL-4+水平升高(P<0.05),IFN-γ+水平无统计学差异。结论:AA的发病与T淋巴细胞异常密切相关,是一种Th1型反应。NKT细胞可代偿调节AA患者IFN-γ和IL-4比例。Objective:To explore the role of intracellular IFN-γ and IL-4 of Th and NKT cells in the pathogenesis of aplastic anemia.Methods:Lymphocyte surface CD molecules were detected by FCM.Intracellular cytokines were measured through intracellular staining.Results:Th lymphocytes in peripheral blood of AA patients decreased.The level of intracellular CD3+CD4+IFN-γ+ and CD3+CD4+IL4+ increased,Th1/Th2 ratio was significant higher(P0.01).NKT cells increased and its level of IL-4+ was obviously higher(P0.05).Conclusion:The amount and function of T lymphocytes are closely related to the pathogenesis of aplastic anemia patients.Aplastic anemia is the Th1-type bias.NKT cells vicariously regulate IFN-γ and IL-4 in patients with AA.
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