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A novel mouse model of atopic dermatitis that is T helper 2 (Th2)-polarized by an epicutaneous allergen

机译:一种新型的特应性皮炎小鼠模型,被表皮过敏原极化的T辅助细胞2(Th2)

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摘要

The pathogenesis of atopic dermatitis (AD) involves T helper 2 (Th2) cells, and effective therapies remain elusive due to the paucity of animal models. We aimed to develop a mouse model of an immune system aberration caused by allergen. Experiments were conducted in two phases. In experiment 1, BALB/c mice were sensitized with one of four chemical allergens – toluene diisocyanate (TDI), hexamethylene diisocyanate (HDI), trimellitic anhydride (TMA), or 2,4-dinitrochlorobenzene (DNCB) – for 3 weeks. Based on results of experiment 1, immunological features were compared between TMA-sensitized BALB/c mice and NC/Nga mice, after exposure to mite extracts, harmful chemicals and detergents in experiment 2. Sensitization by allergen caused a large number of pathological changes in the skin, and an increase in mast cell number. TMA-sensitized BALB/c mice models showed higher sensitivity to an environmental allergen than NC/Nga mice did. Overall, the initial sensitization with TMA leads to disturbances in Th2-mediated immunity.
机译:特应性皮炎(AD)的发病机制涉及T辅助2(Th2)细胞,由于缺乏动物模型,有效的治疗方法仍然难以捉摸。我们旨在开发一种由过敏原引起的免疫系统异常的小鼠模型。实验分两个阶段进行。在实验1中,将BALB / c小鼠用四种化学过敏原之一-甲苯二异氰酸酯(TDI),六亚甲基二异氰酸酯(HDI),偏苯三酸酐(TMA)或2,4-二硝基氯苯(DNCB)敏化3周。根据实验1的结果,在实验2中暴露于螨提取物,有害化学物质和去污剂后,比较了TMA致敏的BALB / c小鼠和NC / Nga小鼠的免疫学特征。过敏原引起的致敏作用引起大量病理变化。皮肤,肥大细胞数量增加。 TMA敏感的BALB / c小鼠模型比NC / Nga小鼠对环境过敏原的敏感性更高。总体而言,TMA的初始致敏作用会导致Th2介导的免疫功能紊乱。

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  • 来源
    《Environmental toxicology and pharmacology》 |2018年第3期|122-130|共9页
  • 作者单位

    Department of Stem Cell and Regenerative Biology, Konkuk University;

    School of Medicine, Konkuk University;

    Department of Beef and Dairy Science, Korea National College of Agricultures and Fisheries;

    Department of Biomedical Sciences, CHA University;

    Department of Stem Cell and Regenerative Biology, Konkuk University;

    Department of Stem Cell and Regenerative Biology, Konkuk University;

    Department of Stem Cell and Regenerative Biology, Konkuk University;

    Department of Stem Cell and Regenerative Biology, Konkuk University;

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