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首页> 外文期刊>The Journal of investigative dermatology. >Epidermal cytokines IL-1beta, TNF-alpha, and IL-12 in patients with atopic dermatitis: response to application of house dust mite antigens.
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Epidermal cytokines IL-1beta, TNF-alpha, and IL-12 in patients with atopic dermatitis: response to application of house dust mite antigens.

机译:特应性皮炎患者的表皮细胞因子IL-1β,TNF-α和IL-12:对应用屋尘螨抗原的反应。

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Epidermal cytokines such as interleukin (IL)-1beta, tumor necrosis factor-alpha, and IL-12 have been described to play a crucial role in the induction and elicitation phase of allergic contact dermatitis upon exposure to haptens. In this study we asked whether these cytokines may also play a role in the epidermis of patients with atopic dermatitis after the application of house dust mite antigens (HDM) to their skin. Epidermal samples were collected by scraping healthy appearing skin of atopic patients and healthy individuals 8 h after the application of an extract of HDM. Sodium lauryl sulfate and saline served as controls. Reverse transcriptase-polymerase chain reaction was performed for IL-1beta, tumor necrosis factor-alpha, IL-12 p35, and IL-12 p40. Exposure to HDM led to a significant upregulation of mRNA of these cytokines in atopic patients only. Whereas IL-1beta and tumor necrosis factor-alpha also showed an upregulation in part of these patients after exposure to the irritant sodium lauryl sulfate, IL-12 p40 mRNA was exclusively enhanced by the application of the allergen. In contrast to IL-12 p40, IL-12 p35 mRNA was not detectable in significant amounts. Interestingly, also in untreated, normal appearing skin of atopic individuals (n = 16), the levels of these cytokines were higher than in normal individuals (n = 8), possibly explaining the increased skin irritability of atopic individuals. Finally, comparing epidermal cytokines in the skin of patients who developed a positive allergen patch test to those who stayed negative, suggests that only expression of IL-1beta mRNA may be a predictive marker for the development of a positive patch test reaction to HDM.
机译:表皮细胞因子,如白介素(IL)-1beta,肿瘤坏死因子-α和IL-12已被描述在接触半抗原后在过敏性接触性皮炎的诱导和诱发阶段起着至关重要的作用。在这项研究中,我们询问在将室内尘螨抗原(HDM)应用于皮肤后,这些细胞因子是否还会在特应性皮炎患者的表皮中发挥作用。应用HDM提取物后8小时,通过刮擦特应性患者和健康个体的健康出现的皮肤来收集表皮样品。月桂基硫酸钠和盐水作为对照。对IL-1β,肿瘤坏死因子-α,IL-12 p35和IL-12 p40进行逆转录酶-聚合酶链反应。暴露于HDM仅导致特应性患者中这些细胞因子的mRNA上调。 IL-1beta和肿瘤坏死因子-α在暴露于刺激性十二烷基硫酸钠后也显示出部分上调,而IL-12 p40 mRNA仅通过过敏原的作用而增强。与IL-12 p40相比,IL-12 p35 mRNA的含量不高。有趣的是,同样在未经治疗的正常人中出现的特应性个体的皮肤(n = 16)中,这些细胞因子的水平高于正常人(n = 8),这可能解释了特应性个体的皮肤过敏性增加。最后,将过敏原斑试验呈阳性的患者与保持过敏原斑呈阴性的患者皮肤中的表皮细胞因子进行比较,表明仅IL-1beta mRNA的表达可能是针对HDM的斑块试验阳性反应的预测指标。

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