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Th1 Th2 and Th17 Cytokine Involvement in Thyroid Associated Ophthalmopathy

机译:Th1Th2和Th17细胞因子参与甲状腺相关性眼病

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摘要

To determine serum cytokine profiles in Graves' disease (GD) patients with or without active and inactive thyroid associated ophthalmopathy (TAO), we recruited 65 subjects: 10 GD only (without TAO), 25 GD + active TAO, 20 GD + TAO, and 10 healthy controls. Liquid chip assay was used to measure serum Th1/Th2/Th17 cytokines including IFN-γ (interferon-gamma), TNF-α (tumor necrosis factor-alpha), IL-1α (interleukin-1 alpha), IL-1Ra (IL-1 receptor antagonist), IL-2, IL-4, IL-6, and IL-17 and two chemokines: RANTES (regulated upon activation, normal T cell expressed and secreted) and IP-10 (IFN-γ-induced protein 10). Serum levels of TSH (thyroid stimulating hormone) receptor autoantibodies (TRAb) were measured using an enzyme linked immunosorbent assay. Compared with healthy controls, TAO patients showed significantly elevated serum levels of IFN-γ, TNF-α, IL-1α, IL-4, IL-6, IL-17, and IP-10. Comparing active and inactive TAO, serum Th1 cytokines IFN-γ and TNF-α were elevated in active TAO, while serum Th2 cytokine IL-4 was elevated in inactive TAO. Serum Th17 cytokine IL-17 was elevated in GD but reduced in both active and inactive TAO. A positive correlation was found between TRAb and IFN-γ, TNF-α, IL-1α, IL-2, IL-4, and IL-6. Taken together, serum Th1/Th2/Th17 cytokines and chemokines reflect TAO disease activity and may be implicated in TAO pathogenesis.
机译:为了确定Graves病(GD)有无活动性和非活动性甲状腺相关性眼病(TAO)的患者的血清细胞因子谱,我们招募了65名受试者:仅10 GD(无TAO),25 GD +活跃TAO,20 GD + TAO,和10个健康对照。液体芯片分析用于测量血清Th1 / Th2 / Th17细胞因子,包括IFN-γ(干扰素-γ),TNF-α(肿瘤坏死因子-α),IL-1α(白介素-1α),IL-1Ra(IL) -1受体拮抗剂),IL-2,IL-4,IL-6和IL-17和两种趋化因子:RANTES(受激活后调节,正常T细胞表达和分泌)和IP-10(IFN-γ诱导的蛋白) 10)。使用酶联免疫吸附测定法测定血清TSH(甲状腺刺激激素)受体自身抗体(TRAb)的水平。与健康对照组相比,TAO患者的血清IFN-γ,TNF-α,IL-1α,IL-4,IL-6,IL-17和IP-10明显升高。比较活性和非活性TAO,活性TAO中血清Th1细胞因子IFN-γ和TNF-α升高,而非活性TAO中血清Th2细胞因子IL-4升高。血清Th17细胞因子IL-17在GD中升高,但在活性和非活性TAO中均降低。在TRAb与IFN-γ,TNF-α,IL-1α,IL-2,IL-4和IL-6之间发现正相关。两者合计,血清Th1 / Th2 / Th17细胞因子和趋化因子反映了TAO疾病的活动,可能与TAO的发病机制有关。

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