Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, Davos, Switzerland.
Eur J Immunol. 2010 May;40(5):1232-40. doi: 10.1002/eji.200940045.
Allergy is a Th2-mediated disease that involves the formation of specific IgE antibodies against innocuous environmental substances. The prevalence of allergic diseases has dramatically increased over the past decades, affecting up to 30% of the population in industrialized countries. The understanding of mechanisms underlying allergic diseases as well as those operating in non-allergic healthy responses and allergen-specific immunotherapy has experienced exciting advances over the past 15 years. Studies in healthy non-atopic individuals and several clinical trials of allergen-specific immunotherapy have demonstrated that the induction of a tolerant state in peripheral T cells represent a key step in healthy immune responses to allergens. Both naturally occurring thymus-derived CD4+CD25+FOXP3+ Treg and inducible type 1 Treg inhibit the development of allergy via several mechanisms, including suppression of other effector Th1, Th2, Th17 cells; suppression of eosinophils, mast cells and basophils; Ab isotype change from IgE to IgG4; suppression of inflammatory DC; and suppression of inflammatory cell migration to tissues. The identification of the molecules involved in these processes will contribute to the development of more efficient and safer treatment modalities.
过敏是一种由 Th2 介导的疾病,涉及针对无害环境物质形成特异性 IgE 抗体。在过去的几十年中,过敏疾病的患病率急剧增加,影响了工业化国家高达 30%的人口。过去 15 年来,对过敏疾病以及非过敏健康反应和过敏原特异性免疫疗法中起作用的机制的理解取得了令人兴奋的进展。在健康非过敏个体中的研究以及几种过敏原特异性免疫疗法的临床试验已经表明,外周 T 细胞中耐受状态的诱导是对过敏原产生健康免疫反应的关键步骤。天然存在的胸腺来源的 CD4+CD25+FOXP3+Treg 和可诱导的 1 型 Treg 通过多种机制抑制过敏的发展,包括抑制其他效应 Th1、Th2、Th17 细胞;抑制嗜酸性粒细胞、肥大细胞和嗜碱性粒细胞;Ab 同种型从 IgE 向 IgG4 的转变;抑制炎症性 DC;以及抑制炎症细胞向组织的迁移。参与这些过程的分子的鉴定将有助于开发更有效和更安全的治疗方式。