Wilson-Konovalov病患儿肝纤维化不同阶段的免疫状态特征

O. Kurbatova, D. Kuptsova, L. M. Bezrukavnikova, T. Radygina, G. Movsisyan, A. Anushenko, A. D. Komarova, A. Potapov, S. Petrichuk, A. Fisenko
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引用次数: 0

摘要

WilsonConovalov病(WCD)的病理是由于铜的排泄受损,从而导致其在组织中的过度积累。高铜血症是WCD的特征。铜对肝组织的毒性作用可表现为肝细胞脂肪变性、肝炎、纤维化和肝硬化。本研究的目的是:根据肝纤维化的分期来估计WD患儿的免疫状态。对53例6 ~ 18岁WCD患者进行了检查。肝纤维化分期采用纤维扫描F502 (echosense,法国)瞬时肝弹性成像进行评估。采用美国Beckman Coulter公司的流式细胞荧光仪(CYTOMICS FC500)检测外周血淋巴细胞免疫状态。测定淋巴区B淋巴细胞(B1和B2群)、NK细胞、辅助T细胞、细胞毒性T淋巴细胞、Th17淋巴细胞、调节性T细胞、活化的辅助T细胞的相对数量。重新计算患者免疫状态的所有指标与年龄相关参考值的偏差百分比。采用AAnalyst 800光谱仪,原子吸收法测定日尿中铜的质量浓度。统计处理采用Statistica10.0程序进行。WCD患者的特点是Т辅助细胞、调节性Т细胞、Th17淋巴细胞和活化的Т辅助细胞增加,细胞毒性Т淋巴细胞和NK细胞相对正常水平下降。B细胞数量与肝纤维化分期无关,均处于正常范围的下限或减少。随着肝纤维化分期的增加,B1淋巴细胞数量增加,B2淋巴细胞数量减少。接受检查的患者尿铜含量在19 - 835 g/天之间,88%的儿童高于参考值,中位数为175 g/天(71-330)。尿铜浓度与免疫状态偏离程度呈正相关(R = 0.63):尿铜浓度随Th17淋巴细胞、B1淋巴细胞和调节性T细胞数量增多而升高,随B2淋巴细胞数量减少而升高。在KaiserFleischer环存在的WCD患儿中,细胞毒性T淋巴细胞数量显著减少(p = 0.034)。WCD患儿的细胞免疫指标是评估肝损害严重程度的信息工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Features of immune status in children with Wilson–Konovalov disease at different stages of liver fibrosis
The pathology in WilsonConovalov disease (WCD) results from impaired excretion of copper, thus leading to its excessive accumulation in tissues. Hypercupreniluria is characteristic to the WCD. Toxic effects of copper on liver tissue can manifest as fatty degeneration of hepatocytes, hepatitis, fibrosis and cirrhosis. Purpose of the present work was as follows: estimation of immune status in children with WD depending on the stage of liver fibrosis. Fifty-three patients with WCD aged 6 to 18 years, were examined. The stage of liver fibrosis was assessed by transient liver elastography using FibroScan F502 (EchoSence, France). The immune status of peripheral blood lymphocytes was examined using CYTOMICS FC500 flow cytofluorimeter (Beckman Coulter, USA). The relative numbers of B lymphocytes (B1 and B2 populations), NK cells, T helper cells, cytotoxic T lymphocytes, Th17 lymphocytes, regulatory T cells, activated T helper cells were assessed in the lymphoid area. All indices of the patients immune status were recalculated for percentage of deviation from the age-dependent reference values. Mass concentration of copper in daily urine was determined by atomic absorption method using AAnalyst 800 spectrometer. Statistical processing was performed by Statistica10.0 program. The WCD patients are characterized by an increase of Т helpers, regulatory Т cells, Th17 lymphocytes and activated Т helpers, along with decrease of cytotoxic Т lymphocytes and NK cells against normal levels. The number of B cells did not depend on the stage of liver fibrosis and was at the lower limit of normal range, or decreased. Upon increase of the liver fibrosis stage, the number of B1 lymphocytes increases and B2 lymphocytes become decreased. The urinary copper content in the examined patients varied from 19 to 835 g/day, being higher than the reference values in 88% of children, with median value of 175 g/day (71-330). A correlation between urinary copper concentration and degree of immune status deviation was revealed (R = 0.63): urinary copper concentration was increased when the number of Th17 lymphocytes, B1 lymphocytes and regulatory T cells became higher, and when the number of B2 lymphocytes decreased. A significant decrease in the population of cytotoxic T lymphocytes (p = 0.034) was observed in children with WCD in the presence of KaiserFleischer ring. Indexes of cellular immunity in children with WCD are an informative tool to assess the severity of liver damage.
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