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作 者:王欣[1] 张明珙[1] 宋素琴[1] 李杰[1] 郭承山[1] 宋强[1] 赵川莉[1] 王惠军 彭军[1] 秦平[1]
机构地区:[1]山东医科大学附属医院
出 处:《中华血液学杂志》1998年第4期181-183,共3页Chinese Journal of Hematology
摘 要:目的:进一步探讨再生障碍性贫血(再障)的免疫发病机制,阐明细胞免疫、造血细胞因子在再障患者中发生变化的基础与临床意义。方法:用单抗试剂盒,采用改良APAAP法及酶联免疫试剂盒,采用ELISA法对38例再障患者及20名正常人外周血T细胞亚群,HLA-DR抗原表达以及外周血单个核细胞(PBMNC)培养上清诱生G-CSF、IL-6、TNFα、IFNα及IL-8水平进行测定。结果:再障患者外周血CD4细胞减低、CD8细胞增高、CD4/CD8降低或倒置,HLA-DR抗原表达率增高。再障患者PBMNC培养上清中G-CSF阳性率减低,IL-6、TNFα、IFNα及IL-8水平增高。相关分析发现G-CSF与CD4细胞及CD4/CD8呈正相关,而与IFNα呈负相关;IL-6与白细胞数及CD4细胞呈负相关;TNFα与CD8细胞呈正相关而与CD4/CD8呈负相关;IL-8与CD8细胞及HLA-DR呈正相关。结论:细胞免疫功能异常及细胞因子网络失调在再障发病中起一定的作用。Objective: To evaluate the effects of cellular immune function and cytokines on the pathogenesis of aplastic anemia(AA) and its clinical significance. Methods: T lymphocyte subsets and HLADR antigen expression in the peripheral blood cells were assayed, and the levels of GCSF,IL6,TNFα,IFNα and IL8 in the PBMNC culture supernatants were determined in 38 AA patients and 20 normal control with APAAP and ELISA methods. Results: CD4+ cells, CD4+/CD8+ cells and GCSF level were lower,and CD8+ cells, HLADR+ cells and IL6,TNFα,IFNα and IL8 levels were higher in AA patients than in normal controls. The level of GCSF was positively correlated with CD4+ cells and CD4+/CD8+ cells and negatively with IFNα level. IL6 level was negatively correlated with WBC count and CD4+ cells. TNFα level was positively correlated with CD8+ cells and negatively with CD4+/CD8+ cells.IL8 level was positively correlated with CD8+ cells and HLADR+ cells. Conclusion: The cellular immune dysfunction and cytokine aberration participate in the pathogenesis of AA.
分 类 号:R556.503[医药卫生—血液循环系统疾病]
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