Department of Pediatric Allergy, School of Medicine, Hacettepe University, Ankara, Turkey.
Allergy. 2013 Feb;68(2):161-70. doi: 10.1111/all.12085. Epub 2012 Dec 18.
The immune system is regulated to protect the host from exaggerated stimulatory signals establishing a state of tolerance in healthy individuals. The disequilibrium in immune regulatory vs effector mechanisms results in allergic or autoimmune disorders in genetically predisposed subjects under certain environmental conditions. As demonstrated in allergen-specific immunotherapy and in the healthy immune response to high-dose allergen exposure models in humans, T regulatory cells are essential in the suppression of Th2-mediated inflammation, maintenance of immune tolerance, induction of the two suppressive cytokines interleukin-10 and transforming growth factor-β, inhibition of allergen-specific IgE, and enhancement of IgG4 and IgA. Also, suppression of dendritic cells, mast cells, and eosinophils contributes to the construction of peripheral tolerance to allergens. This review focuses on mechanisms of peripheral tolerance to allergens with special emphasis on recent developments in the area of immune regulation.
免疫系统受到调节以保护宿主免受过度刺激信号的影响,从而在健康个体中建立耐受状态。在某些环境条件下,免疫调节与效应机制之间的失衡会导致遗传易感性个体发生过敏或自身免疫性疾病。正如在过敏原特异性免疫治疗和人类高剂量过敏原暴露模型的健康免疫反应中所证明的那样,调节性 T 细胞对于抑制 Th2 介导的炎症、维持免疫耐受、诱导两种抑制性细胞因子白细胞介素-10 和转化生长因子-β、抑制过敏原特异性 IgE 以及增强 IgG4 和 IgA 至关重要。此外,抑制树突状细胞、肥大细胞和嗜酸性粒细胞有助于构建对过敏原的外周耐受。本文重点介绍过敏原外周耐受的机制,特别强调免疫调节领域的最新进展。