摘要
为探讨AA的免疫发病机制,阐明细胞因子在AA患者中变化的基础与临床意义,应用ELISA法及APAAP法对38例初治AA患者及20名正常人外周血单个核细胞(PBMNC)培养上清诱生的G-CSF、IL-6、TNFα、IFNα及IL-8进行检测,同时观察外周血象、T细胞亚群及HLA-DR表达。结果:AA患者外周血CD4减低,CD8增高,CD4/CD8减低或倒置,HLA-DR抗原表达率增高。AA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。G-CSF与CD4及CD4/CD8呈正相关而与IFNα呈负相关,IL-6与白细胞数及CD4呈负相关,TNFα与CD8呈正相关而与CD4/CD8呈负相关,IL-8与CD8及HLA-DR呈负相关,证明细胞免疫功能异常及细胞因子网络失调在AA发病中起重要作用,激活的CD8细胞可以抑制造血,多种因素引起的细胞因子紊乱最终引发AA。
To evaluate the effects of cell immune function and cytokines on the pathogenesis of aplastic anemia(AA)and the clinical significance,T lymphocte subsets,HLADR antigen and GCSF,IL6,TNFα,IFNα,IL8 in the PBMNC culture supernatants in 38 AA patients and 20 normal persons were examined with APAAP and ELISA methods.CD4 cell,CD4/CD8 and GCSF in AA patients were lower,CD8,HLADR and IL6,TNFα,IL8 were higher than that of normal control.The level of GCSF was positively associated with CD4,CD4/CD8 and negatively associated with IFNα.IL6 was negatively associated with WBC and CD4.TNFα was positively correlated with CD8 and negatively correlated with CD4/CD8.IL8 was negatively with CD8 and HLA-DR.The study provide envidence that the cell immune and cytokines anticipate in the pathogenesis of AA.
出处
《山东医科大学学报》
1997年第4期321-325,共5页
Acta Academiae Medicinae Shandong