小淋巴细胞群在糖原储存病儿童肝纤维化发展中的作用

O. Kurbatova, S. Petrichuk, G. Movsisyan, Daria G. Kuptsova, T. Radygina, A. Anushenko, E. Semikina, A. Potapov
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引用次数: 0

摘要

糖原储存病(GSD)是一种罕见的疾病,它改变了身体使用和储存糖原的方式。目的:评价肝型糖原病患儿小群淋巴细胞的含量及其比例与肝纤维化分期的关系。对148例年龄为Me=7,7[3,9;11,8]的GSD患儿进行了检查。对照组为54名健康儿童。肝纤维化分期在FibroScan F502设备(echoense,法国)上进行。淋巴细胞免疫分型在美国Beckman Coulter公司的CYTOMICS FC500上进行。淋巴细胞群指标以偏离年龄标准的百分比进行分析。在GSD患儿中,肝纤维化程度随年龄增加而增加(R=0.57)。GSD患儿Treg含量处于年龄正常值的下限,且与肝纤维化分期无关。从F1期开始,肝纤维化各阶段Th17和Thact淋巴细胞含量均显著高于对照组。随着肝纤维化分期的增加,Thact和Th17含量超过正常值上限的患者比例增加(PF0-F4=0.021, PF0-F4=0.012)。各年龄组GSD患者Th17/Treg和Thact/Treg比值均较对照组升高,Th17/Treg和Thact/Treg比值随年龄的增长而升高。GSD患儿肝纤维化分期指标分析显示,从F0期到F1、F2、F3、F4期Thact/Treg比值显著升高(PF0-F4=0.000)。从F0期到F1、F2、F3期Th17/Treg指数升高(PF0-F3=0.000)。Thact和Th17淋巴细胞含量的增加,以及Th17/Treg和Thact/Treg指数随肝纤维化分期的增加,可作为评估肝脏纤维化变化的附加工具。免疫指标客观地反映了肝型GSD患者病情的严重程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of minor lymphocyte populations in development of liver fibrosis in children with glycogen storage disease
Glycogen storage disease (GSD) is a rare condition that changes the way the body uses and stores glycogen. Objective: to evaluate the content of small populations of lymphocytes and their ratios in children with hepatic forms of glycogen disease depending on the stage of liver fibrosis. 148 children with GSD at the age of Me=7,7 [3,9;11,8] were examined. The comparison group consisted of 54 healthy children. The stage of liver fibrosis was carried out on the FibroScan F502 device (EchoSence, France). Immunophenotyping of lymphocytes was performed on CYTOMICS FC500 (Beckman Coulter, USA). Indicators of lymphocyte populations were analyzed as a percentage of deviation from the age norm. In children with GSD, an increase in the degree of liver fibrosis was revealed from age (R=0.57). Treg content in children with GSD was at the lower limit of the age norm and did not depend on the stage of liver fibrosis. The content of Th17 and Thact lymphocytes was significantly higher than that of the comparison group at all stages of liver fibrosis, starting from stage F1. With an increase in the stage of liver fibrosis, there was an increase in the proportion of patients with Thact and Th17 content exceeding the upper limit of the normative values (PF0-F4=0.021 and PF0-F4=0.012, respectively). An increase in Th17/Treg and Thact/Treg ratios was revealed in patients with GSD relative to the comparison group in all age groups, the dynamics of Th17/Treg and Thact/Treg ratios was characterized by their increase with age. Analysis of indicators depending on the stage of liver fibrosis in children with GSD revealed a significant increase in the Thact/Treg ratio from stage F0 to stages F1, F2, F3 and F4 (PF0-F4=0.000). The Th17/Treg index increased from stage F0 to stages F1, F2, F3 (PF0-F3=0.000). An increase in the content of Thact and Th17 lymphocytes, as well as Th17/Treg and Thact/Treg indices with an increase in the stage of liver fibrosis can be used as an additional tool in assessing fibrotic changes in the liver. Immunological indicators objectively reflect the severity of the patient's condition with hepatic forms of GSD.
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