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小儿镰状细胞病患者在血管闭塞性危象和稳定状态期间的血清白细胞介素-6、白细胞介素-10和肿瘤坏死因子α水平。

Serum IL-6, IL-10, and TNFα levels in pediatric sickle cell disease patients during vasoocclusive crisis and steady state condition.

作者信息

Sarray Sameh, Saleh Layal R, Lisa Saldanha F, Al-Habboubi Hebah H, Mahdi Najat, Almawi Wassim Y

机构信息

Department of Medical Biochemistry, Arabian Gulf University, Manama, Bahrain.

Department of Medical Biochemistry, Arabian Gulf University, Manama, Bahrain.

出版信息

Cytokine. 2015 Mar;72(1):43-7. doi: 10.1016/j.cyto.2014.11.030. Epub 2015 Jan 5.

Abstract

Vaso-occlusive crisis (VOC) is a significant complication of sickle cell disease (SCD), and altered production of pro-inflammatory and anti-inflammatory molecules contributed to its pathogenesis. In view of the association of chronic inflammation with VOC onset, and given the capacity of interleukin (IL)-10 as anti-inflammatory, and IL-6, and TNFα as pro-inflammatory cytokines, we tested the association of altered IL-10, IL-6, and TNFα secretion with VOC pathogenesis and its severity. Study subjects comprised 147 SCD patients with active VOC (VOC Group), and 63 pain-free SCD patients for at least 9 months before blood collection (Steady-state Group). Serum cytokine concentrations were determined by ELISA. IL-10 levels were significantly reduced, while IL-6 levels were increased in VOC compared to Steady-state groups; serum TNFα levels were comparable between both groups. There was enrichment of low IL-10, but high IL-6 and TNFα quartiles in VOC Group, which translated into increased VOC risk. In contrast, high IL-10, but low IL-6 and TNFα quartiles were seen in Steady-state Group. Correlation analysis demonstrated significant association between reduced IL-10 levels and the frequency, type, severity, and duration of VOC and requirement for hydroxyurea treatment, while IL-6 correlated with duration of VOC episodes. Our data support strong association of reduced IL-10 and increased IL-6 levels with VOC, and their modulation of VOC-related parameters.

摘要

血管闭塞性危机(VOC)是镰状细胞病(SCD)的一种重要并发症,促炎和抗炎分子产生的改变促成了其发病机制。鉴于慢性炎症与VOC发作之间的关联,并且考虑到白细胞介素(IL)-10具有抗炎作用,而IL-6和肿瘤坏死因子α(TNFα)是促炎细胞因子,我们测试了IL-10、IL-6和TNFα分泌改变与VOC发病机制及其严重程度之间的关联。研究对象包括147例患有活动性VOC的SCD患者(VOC组)和63例在采血前至少9个月无疼痛的SCD患者(稳定状态组)。通过酶联免疫吸附测定法(ELISA)测定血清细胞因子浓度。与稳定状态组相比,VOC组中IL-10水平显著降低,而IL-6水平升高;两组之间血清TNFα水平相当。VOC组中低IL-10、高IL-6和TNFα四分位数增多,这转化为VOC风险增加。相比之下,稳定状态组中出现高IL-10、低IL-6和TNFα四分位数。相关性分析表明,IL-10水平降低与VOC的频率、类型、严重程度和持续时间以及羟基脲治疗需求之间存在显著关联,而IL-6与VOC发作的持续时间相关。我们的数据支持IL-10降低和IL-6水平升高与VOC密切相关,以及它们对VOC相关参数的调节作用。

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