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首页> 外文期刊>The Journal of investigative dermatology. >Afferent and Efferent Phases of Allergic Contact Dermatitis (ACD) Can Be Induced After a Single Skin Contact with Haptens: Evidence Using a Mouse Model of Primary ACD.
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Afferent and Efferent Phases of Allergic Contact Dermatitis (ACD) Can Be Induced After a Single Skin Contact with Haptens: Evidence Using a Mouse Model of Primary ACD.

机译:皮肤与半抗原单次接触后,可诱发过敏性接触性皮炎(ACD)的传入和传出阶段:使用原发性ACD小鼠模型的证据。

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Allergic contact dermatitis is a T cell-mediated delayed type hypersensitivity reaction that occurs upon hapten challenge in sensitized individuals. The inflammatory response in classical allergic contact dermatitis requires both a sensitization phase and an elicitation phase responsible for the recruitment and activation of specific T cells at the site of hapten skin challenge. Conversely, previously unsensitized patients may develop a "primary allergic contact dermatitis" after the first skin contact with potent contact sensitizers leading to a skin inflammation with all the features of classical allergic contact dermatitis. In this study we used an experimental murine model, referred to as contact hypersensitivity, to study the pathophysiology of primary allergic contact dermatitis and its relationship to classical allergic contact dermatitis. We show that one epicutaneous application of a nonirritant dose of hapten (2,4-dini-trofluorobenzene, fluorescein isothiocyanate) was sufficient to induce an optimal allergic contact dermatitis reaction at the site of primary contact with the hapten without subsequent challenge. As in classical allergic contact dermatitis, the skin inflammation in primary allergic contact dermatitis was mediated by interferon-gamma producing, CD8+ effector T cells that were induced in the draining lymph nodes at day 5 postsensitization and downregulated by CD4+ T cells. Reverse transcription-polymerase chain reaction analysis revealed that the primary allergic contact dermatitis reaction was mediated by a recruitment of CD8+ T cells at the sensitization skin site at day 6 postsensitization. Analysis of the fate of the hapten fluorescein isothiocyanate applied once on the skin revealed its persistence in the epidermis for up to 14 d after skin painting. These results suggest that the development of primary allergic contact dermatitis (i.e., without secondary challenge) is associated with persistence of the hapten in the skin, which allows the recruitment and activation of CD8+ T cells at the site of the single hapten application.
机译:过敏性接触性皮炎是T细胞介导的迟发型超敏反应,在致敏个体中半抗原攻击后发生。经典变应性接触性皮炎的炎症反应需要致敏期和诱导期,它们负责在半抗原皮肤攻击部位募集和激活特定的T细胞。相反,先前未致敏的患者在首次与强效接触敏化剂皮肤接触后会发展为“原发性过敏性接触性皮炎”,导致皮肤发炎,具有典型的过敏性接触性皮炎的所有特征。在这项研究中,我们使用称为接触性超敏反应的实验性小鼠模型来研究原发性过敏性接触性皮炎的病理生理及其与经典过敏性接触性皮炎的关系。我们表明,一种非刺激剂量的半抗原(2,4-二氨基-三氟苯,异硫氰酸荧光素)的表皮应用足以在与半抗原的主要接触部位诱导出最佳的过敏性接触性皮炎反应,而没有随后的挑战。如在经典的过敏性接触性皮炎中一样,原发性过敏性接触性皮炎中的皮肤炎症是由产生干扰素-γ的CD8 +效应T细胞介导的,CD8 +效应T细胞在致敏后第5天在引流淋巴结中被诱导,并被CD4 + T细胞下调。逆转录-聚合酶链反应分析表明,原发性过敏性接触性皮炎反应是由致敏后第6天在致敏皮肤部位募集CD8 + T细胞介导的。对一次施用在皮肤上的半抗原异硫氰酸荧光素的命运进行的分析表明,皮肤涂漆后,其在表皮中的持久性长达14 d。这些结果表明原发性过敏性接触性皮炎(即没有继发性攻击)的发展与半抗原在皮肤中的持久性有关,这允许在单次半抗原施用部位募集和激活CD8 + T细胞。

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