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免疫性血小板减少症:儿童和成人的血清细胞因子水平。

Immune thrombocytopenia: serum cytokine levels in children and adults.

机构信息

Department of Pediatric Hematology, Oncology, Immunology and Medical Genetics, Clinical Hospital Center Split, Medical School, University of Split, Split, Croatia.

出版信息

Med Sci Monit. 2013 Sep 27;19:797-801. doi: 10.12659/MSM.884017.

DOI:10.12659/MSM.884017
PMID:24072209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3789580/
Abstract

BACKGROUND

Immune thrombocytopenia (ITP) is an immune-mediated platelet disorder in which autoantibody-coated platelets are removed from the blood by monocytic phagocytes and there is impaired platelet production. There is a delicate balance of specific cytokine levels, which has an important role in the immune system and is known to be deregulated in autoimmune diseases. This study was designed to investigate the differences in Th cytokine levels between children and adults with newly diagnosed ITP and to compare these profiles to those found in healthy, age-matched controls.

MATERIAL/METHODS: The concentration of IL-1alpha, IL-2, IL-3, IL-4, IL-6, IL-10, TNF-alpha, IFN-alpha, and IFN-alpha in serum specimens was analyzed by enzyme-linked immunosorbent assay.

RESULTS

At the time of ITP diagnosis, children showed significantly lower serum levels of interleukin IL-2 and tumor necrosis factor TNF-alpha and higher serum level of IL-3 than healthy controls. Serum level of IL-4 in adult ITP patients was higher than those in control subjects. When compared with adults, children with ITP had lower serum level of IL-4, IL-6 and IFN-alpha, and higher level of IFN-alpha.

CONCLUSIONS

Significant differences in serum cytokine levels between pediatric patients and healthy controls indicate that cytokine disturbances--especially changes in IL-2, IL-3 and TNF-alpha--might be involved in the pathogenesis of newly diagnosed ITP. TNF-alpha is the most informative variable for discrimination between healthy children and those with ITP.

摘要

背景

免疫性血小板减少症(ITP)是一种由自身抗体包被的血小板被单核吞噬细胞从血液中清除,导致血小板生成受损的免疫介导的血小板疾病。特定细胞因子水平之间存在着微妙的平衡,这在免疫系统中起着重要作用,并且已知在自身免疫性疾病中失调。本研究旨在研究新诊断为 ITP 的儿童和成人之间 Th 细胞因子水平的差异,并将这些特征与健康、年龄匹配的对照进行比较。

材料/方法:采用酶联免疫吸附试验分析血清标本中白细胞介素 IL-1alpha、IL-2、IL-3、IL-4、IL-6、IL-10、TNF-alpha、IFN-alpha 和 IFN-alpha 的浓度。

结果

在 ITP 诊断时,儿童的血清白细胞介素 IL-2 和肿瘤坏死因子 TNF-alpha 水平显著降低,IL-3 水平显著升高,而健康对照组则较低。成人 ITP 患者的血清 IL-4 水平高于对照组。与成人相比,ITP 患儿的血清 IL-4、IL-6 和 IFN-alpha 水平较低,IFN-alpha 水平较高。

结论

儿科患者与健康对照组之间血清细胞因子水平的显著差异表明,细胞因子紊乱-尤其是 IL-2、IL-3 和 TNF-alpha 的变化-可能参与了新诊断 ITP 的发病机制。TNF-alpha 是区分健康儿童和 ITP 患儿的最具信息量的变量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/330d/3789580/1561705be265/medscimonit-19-797-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/330d/3789580/1561705be265/medscimonit-19-797-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/330d/3789580/1561705be265/medscimonit-19-797-g001.jpg

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