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作 者:段国荣[1] 周永兴[2] 赵怡生[1] 李建元[1] 付建军[1] 李永勤[1] 田亚莉[1]
机构地区:[1]西安市中心医院感染科 [2]第四军医大学唐都医院感染病科,西安710003
出 处:《胃肠病学和肝病学杂志》2006年第1期65-68,共4页Chinese Journal of Gastroenterology and Hepatology
基 金:西安市科技攻关项目(SF200216)
摘 要:目的观察成人急性HBV感染后免疫指标的变化并进行不同转归比较。方法选择29例急性乙肝患者和20例正常对照者,采用双抗体酶联分析法检测外周血细胞因子IL2、IFNγ、IL4、IL10和IL12的水平;通过流式细胞仪观察外周血T淋巴细胞亚群变化;采用抗人T淋巴细胞单克隆抗体间接免疫荧光法观察外周血T淋巴细胞膜IFNγ和IL4的表达。结果29例HBeAg全部转阴,8例HBsAg未转阴。在HBsAg转阴组,病程早期和中期血清IL2、IFNγ、IL4及IL12水平增高与正常组比P<0.05,中期IL4下降与早期比P<0.05,晚期IL2、IFNγ、IL4及IL12下降与中期比P<0.05;未转阴组各期IL4水平增高与正常组比P<0.05。转阴组早期Th1/Th2降低与对照组比P<0.05,未转阴组各期Th1/Th2降低与对照组比P<0.05。未转阴组中5例入院时HBVDNA<103且IFNγ水平明显低。两组CD4+/CD8+变化趋势不同。转阴组早期和中期IL4膜表达高于正常对照组,中期IL4表达低于早期,晚期IL4表达低于中期,P值均<0.05。未转阴组各期IL4表达高于正常对照组,P<0.05,各期之间IL4表达无统计学差异。结论IFNγ升高与疾病恢复相关。持续高水平的IL4表达易致慢性化。恢复Th1/Th2细胞的平衡可能是控制乙型肝炎慢性化的一条途径。CD4+/CD8+失调可能影响机体清除病毒的能力,导致感染的持续。Objective To explore the natural consequence of acute hepatitis B in adult and chang of immune markers. Methods The serum levels of IL-2, IFN-γ, IL-4 ,IL-10 and IL-12, were measured by using enzymelinked immumosorbent assay, T lymphocyte subsets of peripheral blood were observed by fluorescence activated cell sorting(FACS). The activitiesof IFN-γ and IL-4 of peripheral blood T lymphocyte members were studied by indirect immunofluorescent antibody method (IFAT). Results The disappearance of HBeAg occurred in all 29 patients, un-disappearance of HBsAg occurred in 8 of 29 patients. In group of seroconversion( disappearance of HBsAg), IL-2, IFN-γ, IL-4 and IL-12 were significantly increased as compared with normal controls ( P 〈 0.05) within 2 weeks and 4-6 weeks. The serum levels of IL-4 within 4-6 weeks was decreased as compared with that of IL-4 within 2 weeks ( P 〈 0.05). The serum levels of IL-2,IFN - γ,IL-4 and IL-12( 〉 8 weeks) were decreased as compared with that within 4-6 weeks ( P 〈 0.05). In group of no seroconversion (without - disappearance of HBsAg), the variety of IL-4 was different as compared with that of seroconversion. The IL-4 concentrations with in different phases were increased as compared with normal controls( P 〈 0.05). No difference were showed in decreased IL-4 levels among different phases. In group of seroconversion, there exists a low ratio of Th1/Th2 within 2 weeks when compared with normal controls( P 〈 0.05). However, In Group of no seroconversion, the ratio of Th1/Th2 in different phases was decreased as compared with normal controls( P 〈 0.05). At the time of the initial, the serum levels of IFN-γ,when HBV-DNA 〈 10^3, was less than that when HBV-DNA≥ 10^6. Maximal reduction in HBV replication(HBV-DNA 〈 10^3) occurred in 5/8 patients in group of no seroconversion. In group of seroconversion, the CD4^ +/CD8^ + ratio at the time of the initial and in 4-6 weeks was decreased as compared with normal controls �
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