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骨桥蛋白与变应性疾病:病理生理学及对诊断和治疗的影响。

Osteopontin and allergic disease: pathophysiology and implications for diagnostics and therapy.

机构信息

University of Ulm, Department of Dermatology and Allergy, Maienweg 12, D-89081 Ulm, Germany.

出版信息

Expert Rev Clin Immunol. 2011 Jan;7(1):93-109. doi: 10.1586/eci.10.82.

Abstract

Osteopontin (OPN) is a phosphoglycoprotein that is expressed by various immune cells in a secreted and intracellular form. It has cytokine, chemotactic and cell signaling functions enhancing Th1 and Th17 immunity and protects against apoptosis. Recent studies found OPN to be modulatory in cell-mediated and immediate-type allergic diseases. In allergic asthma, OPN enhances sensitization but downmodulates Th2-driven IL-4-dominated inflammation. The finding that OPN expression is augmented during specific immunotherapy supports a Th2 suppressive effect of OPN. In Th1-driven delayed-type allergy, such as allergic contact dermatitis, OPN supports dendritic cell migration and IL-12 expression and is secreted by T effector cells and keratinocytes, augmenting Th1-mediated allergy and supporting disease chronification. There are numerous missing links as to how OPN variants modulate allergic inflammation through different OPN receptors. OPN research in allergy is an interesting, rapidly expanding field that has high potential for translational research.

摘要

骨桥蛋白(OPN)是一种磷酸糖蛋白,以分泌型和细胞内型的形式由各种免疫细胞表达。它具有细胞因子、趋化和细胞信号功能,增强 Th1 和 Th17 免疫,并防止细胞凋亡。最近的研究发现 OPN 在细胞介导和即刻型过敏疾病中具有调节作用。在过敏性哮喘中,OPN 增强致敏作用,但下调 Th2 驱动的以 IL-4 为主的炎症。在特异性免疫治疗过程中发现 OPN 表达增加,支持 OPN 的 Th2 抑制作用。在 Th1 驱动的迟发型过敏中,如过敏性接触性皮炎,OPN 支持树突状细胞迁移和 IL-12 表达,并由 T 效应细胞和角质形成细胞分泌,增强 Th1 介导的过敏反应并支持疾病慢性化。OPN 变体如何通过不同的 OPN 受体调节过敏炎症存在许多未知环节。过敏领域的 OPN 研究是一个有趣且快速发展的领域,具有很高的转化研究潜力。

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