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Changes in peripheral T-lymphocyte subsets in acute-on-chronic liver failure patients with artificial liver support system

机译:人工肝支持系统对急慢性肝衰竭患者外周血T淋巴细胞亚群的影响

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Background/Aims: HBV-related acute-on-chronic liver failure (AoCLF) is associated with a high mortality rate. An artificial liver support system (ALSS) is a newly emerging therapeutic option, which can be implemented in routine patient care. In order to determine if any pretreatment immunological parameter could be an indicator to evaluate immune states for the outcome of the AoCLF patients, we analyzed the relationship between the level of T-lymphocyte subsets (CD4+, CD8+, CD4/CD8 ratio) and its therapeutic effect and prognosis. Methodology: Sixty-three patients with AoCLF were enrolled in 2 groups (ALSS plus routine-care, n=29 and routine-care only, n=34). In the ALSS group, there were 17 survivors (17/29), while in the routine-care group there were 11 survivors (11/34), both after 30 days of treatment. Twenty-three healthy donors were used as the control group. The number of CD4 and CD8 T cells was detected by flow cytometry and the ratio of CD4/ CD8 was calculated on admission and on days 7, 14, 21 and 30, during hospitalization. Results: More dramatic increased CD4/CD8 ratio in the ALSS survivors (form 0.92±0.18 to 1.26±0.24, p<0.01) than the medical survivors (form 0.86±0.16 to 1.09±0.16, p<0.05) after 30 days of treatment. A declined tendency was observed in non- survivors. Conclusions: T-lymphocyte subsets may be important in the pathogenesis of the AoCLF and ALSS may represent a reliable hepatic support device for Ao-CLF.
机译:背景/目的:HBV相关的慢性慢性肝功能衰竭(AoCLF)与高死亡率相关。人工肝支持系统(ALSS)是一种新兴的治疗选择,可以在常规患者护理中实施。为了确定是否有任何预处理免疫学指标可以作为评估AoCLF患者预后的免疫状态的指标,我们分析了T淋巴细胞亚群水平(CD4 +,CD8 +,CD4 / CD8比)与其治疗方法之间的关系。效果和预后。方法:将63例AoCLF患者分为2组(ALSS加常规治疗,n = 29,仅常规治疗,n = 34)。在ALSS组中,治疗30天后有17名幸存者(17/29),而在常规护理组中有11名幸存者(11/34)。二十三个健康的供体被用作对照组。通过流式细胞术检测CD4和CD8 T细胞的数目,并在住院期间以及住院期间的第7、14、21和30天计算CD4 / CD8的比率。结果:治疗30天后,ALSS幸存者的CD4 / CD8比值显着增加(从0.92±0.18至1.26±0.24,p <0.01)比医疗幸存者(从0.86±0.16至1.09±0.16,p <0.05)高。在非幸存者中观察到下降的趋势。结论:T淋巴细胞亚群可能在AoCLF的发病机制中起重要作用,而ALSS可能代表Ao-CLF的可靠肝支持装置。

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