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首页> 外文期刊>Contact dermatitis >Characterization of lymphocyte subpopulations and cytokine profiles in peripheral blood of nickel-sensitive individuals with systemic contact dermatitis after oral nickel exposure.
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Characterization of lymphocyte subpopulations and cytokine profiles in peripheral blood of nickel-sensitive individuals with systemic contact dermatitis after oral nickel exposure.

机译:口服镍暴露后对全身接触性皮炎的镍敏感个体的外周血中淋巴细胞亚群和细胞因子谱的表征。

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摘要

Several studies have shown that oral nickel exposure can elicit systemic contact dermatitis (SCD) in nickel-sensitive individuals. The current study describes some of the immunological mechanisms underlying such nickel-allergic reactions elicited by oral exposure to nickel. Following oral exposure to graded concentrations of nickel or placebo, blood samples were taken from nickel-sensitive individuals and from non-nickel-sensitive controls. T-cell subtypes (CD3(+), CD4(+), CD8(+) and CD45RO(+)), expression of skin-homing receptor, cutaneous lymphocyte-associated antigen (CLA) and cytokine profiles [interleukin (IL)-2, IL-4, IL-5, IL-6, IL-10, interferon-gamma and tumour necrosis factor-alpha] were investigated. A definite dose-response reaction pattern to oral nickel exposure was observed among nickel-sensitive individuals. Nickel-sensitive individuals whose dermatitis flared after oral challenge with nickel showed significant decreases in fractions of CD3(+) CD45RO(+) CLA(+) and CD8(+) CD45RO(+) CLA(+) blood lymphocytes, suggesting migration of CD8(+)'memory' CLA(+) T lymphocytes from the blood to peripheral tissues. Only those nickel-sensitive individuals who clinically reacted to oral challenge with nickel (4 mg) had elevated levels of IL-5 in the serum, indicating an activation of type 2 T lymphocytes in the peripheral blood. In conclusion, the study indicates that CD8(+) CD45RO(+) CLA(+) T lymphocytes and T lymphocytes with a type 2 cytokine profile are involved in SCD elicited by nickel.
机译:几项研究表明,口服镍暴露可引起对镍敏感的人发生全身性接触性皮炎(SCD)。当前的研究描述了通过口服镍引起的此类镍过敏反应的一些免疫学机制。口服暴露于分级浓度的镍或安慰剂后,从对镍敏感的个体和对非镍敏感的对照组中采集血样。 T细胞亚型(CD3(+),CD4(+),CD8(+)和CD45RO(+)),皮肤归巢受体的表达,皮肤淋巴细胞相关抗原(CLA)和细胞因子谱[白介素(IL)-参照图2,研究了IL-4,IL-5,IL-6,IL-10,干扰素-γ和肿瘤坏死因子-α。在对镍敏感的个体中观察到对口服镍暴露的确定的剂量反应模型。对镍敏感的个体,经镍口服刺激后皮炎发作,表现出CD3(+)CD45RO(+)CLA(+)和CD8(+)CD45RO(+)CLA(+)血淋巴细胞分数的显着降低,提示CD8迁移(+)“记忆” CLA(+)T淋巴细胞从血液到周围组织。只有那些对镍(4 mg)口服挑战产生临床反应的对镍敏感的个体血清中的IL-5水平升高,表明外周血中2型T淋巴细胞被激活。总之,该研究表明,镍诱发的SCD涉及CD8(+)CD45RO(+)CLA(+)T淋巴细胞和具有2型细胞因子谱的T淋巴细胞。

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