首页> 外文期刊>Scandinavian journal of immunology. >Interleukin-12 and tumour necrosis factor-alpha equilibrium is a prerequisite for clinical course free from late complications in children with type 1 diabetes mellitus.
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Interleukin-12 and tumour necrosis factor-alpha equilibrium is a prerequisite for clinical course free from late complications in children with type 1 diabetes mellitus.

机译:白细胞介素12和肿瘤坏死因子-α平衡是无1型糖尿病儿童晚期并发症临床过程的前提。

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The objective of the study was to analyse levels of IL-12 and TNF-alpha and relate the findings to the occurrence of microangiopathy in children with type 1 diabetes mellitus (DM). We examined a group of 123 children with type 1 DM. Serum levels of IL-12 and TNF-alpha were measured by an immunoenzymatic ELISA technique. TNF-alpha and IL-12 tended to be simultaneously present or absent in the sera of 50% of the children who had not developed complications, thus indicating a state of cytokine's equilibrium. Among the patients with an established retinopathy, two IL-12/TNF-alpha combinations were visible. Either a lack of detectable TNF-alpha was accompanied by measurable IL-12 serum concentrations or TNF-alpha incidence was associated with undetectable IL-12 values. Simultaneous lack of TNF-alpha and presence of IL-12 was associated with a better prognosis as these patients had a significantly lower albumin excretion rate. The state of equilibrium between TNF-alpha and IL-12 is beneficial in patients at early stages of the disease, prior to the occurrence of complications. Shifting the equilibrium towards TNF-alpha seems to promote late complications. It may suggest that a disharmony between pro- and anti-angiogenic function of these cytokines underlie the mechanism by which TNF-alpha and IL-12 shape the disease course.
机译:这项研究的目的是分析IL-12和TNF-α的水平,并将这些发现与1型糖尿病(DM)儿童的微血管病变的发生联系起来。我们检查了123名1型DM儿童。血清IL-12和TNF-α水平通过免疫酶联免疫吸附测定技术测定。在没有发生并发症的50%的儿童血清中,TNF-α和IL-12倾向于同时存在或不存在,因此表明细胞因子处于平衡状态。在已经确定的视网膜病变患者中,可以看到两种IL-12 /TNF-α组合。缺乏可检测的TNF-α伴有可测量的IL-12血清浓度,或者TNF-α发生率与不可检测的IL-12值相关。同时缺乏TNF-α和存在IL-12与更好的预后相关,因为这些患者的白蛋白排泄率明显较低。 TNF-α和IL-12之间的平衡状态在疾病早期,并发症发生之前的患者中是有益的。将平衡向TNF-α转移似乎会促进晚期并发症。这可能表明这些细胞因子的促血管生成和抗血管生成功能之间的不和谐是TNF-α和IL-12改变疾病进程的机制的基础。

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