首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Induction of autoallergy with an environmental allergen mimicking a self protein in a murine model of experimental allergic asthma.
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Induction of autoallergy with an environmental allergen mimicking a self protein in a murine model of experimental allergic asthma.

机译:在实验性过敏性哮喘的小鼠模型中,模拟环境自身蛋白的环境变应原诱导自体变态反应。

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BACKGROUND: Allergy and autoimmunity are traditionally considered as 2 exclusive entities related to the development of either T(H)2-dominated or T(H)1-dominated immune responses. OBJECTIVE: This study investigated whether allergic sensitization to a foreign antigen mimicking a self protein can induce allergy accompanied by an autoimmune response. METHODS: BALB/c mice were sensitized to human alpha-NAC, an evolutionary conserved component of the nascent polypeptide-associated complex, recently identified as an IgE-reactive autoantigen in patients with severe forms of atopy. By using nitrocellulose-blotted murine lung and skin extracts, purified recombinant human as well as murine alpha-NAC and murine alpha-NAC-derived synthetic peptides, the IgE, IgG1, and IgG2a antibody responses were measured, and their epitope specificity was mapped. RESULTS: Cross-reactivity of IgE and IgG antibodies with murine alpha-NAC was found in mice sensitized with human alpha-NAC. The biological relevance of the antibody response was demonstrated by the induction of immediate skin reactions in sensitized mice and by the fact that skin sensitivity could be passively transferred with serum to naive mice. Antigen challenge of sensitized mice resulted in airway inflammation accompanied by eosinophil and neutrophil accumulation, airway hyperresponsiveness to methacholine and perivasculitis of lung veins. CONCLUSION: Our data demonstrate that sensitization with a foreign antigen mimicking self can induce an allergic immune response of a mixed T(H)2 and T(H)1 profile that is associated with autoreactivity. Cross-sensitization to self may represent an important pathomechanism involved in the maintenance of severe and chronic forms of allergy.
机译:背景:过敏和自身免疫在传统上被认为是两个与T(H)2为主或T(H)1为主的免疫反应发展有关的排他性实体。目的:本研究调查了对模仿自身蛋白的外源抗原的过敏性致敏反应是否可引起过敏并伴有自身免疫反应。方法:BALB / c小鼠对人α-NAC敏感,α-NAC是新生多肽相关复合物的进化保守成分,最近被鉴定为患有重症特应性疾病的IgE反应性自身抗原。通过使用硝化纤维素印迹的鼠肺和皮肤提取物,纯化了重组人以及鼠α-NAC和鼠α-NAC衍生的合成肽,测量了IgE,IgG1和IgG2a抗体反应,并绘制了它们的表位特异性。结果:在人α-NAC致敏的小鼠中发现了IgE和IgG抗体与鼠α-NAC的交叉反应。抗体反应的生物学相关性通过在致敏小鼠中引起立即的皮肤反应以及皮肤敏感性可以通过血清被动转移至幼稚小鼠这一事实得到证明。致敏小鼠的抗原攻击导致气道发炎,并伴有嗜酸性粒细胞和中性粒细胞积聚,气道对乙酰甲胆碱的高反应性和肺静脉血管炎。结论:我们的数据表明,用模仿自身的外源抗原致敏可以诱导与自身反应性相关的混合的T(H)2和T(H)1分布的变态免疫反应。对自我的交叉敏化可能是维持严重和慢性过敏形式的重要病理机制。

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