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哮喘中的免疫机制。

Immunologic mechanisms in asthma.

机构信息

Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, Davos, Switzerland; Allergy and Clinical Immunology, Department of Medicine, Phramongkutklao Hospital, Bangkok, Thailand.

Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, Davos, Switzerland; Christine Kühne-Center for Allergy Research and Education (CK-CARE), Davos, Switzerland; Ankara University School of Medicine, Department of Chest Diseases Division of Clinical Immunology and Allergic Diseases, Ankara, Turkey.

出版信息

Semin Immunol. 2019 Dec;46:101333. doi: 10.1016/j.smim.2019.101333. Epub 2019 Nov 6.

Abstract

Asthma is a chronic airway disease, which affects more than 300 million people. The pathogenesis of asthma exhibits marked heterogeneity with many phenotypes defining visible characteristics and endotypes defining molecular mechanisms. With the evolution of novel biological therapies, patients, who do not-respond to conventional asthma therapy require novel biologic medications, such as anti-IgE, anti-IL-5 and anti-IL4/IL13 to control asthma symptoms. It is increasingly important for physicians to understand immunopathology of asthma and to characterize asthma phenotypes. Asthma is associated with immune system activation, airway hyperresponsiveness (AHR), epithelial cell activation, mucus overproduction and airway remodeling. Both innate and adaptive immunity play roles in immunologic mechanisms of asthma. Type 2 asthma with eosinophilia is a common phenotype in asthma. It occurs with and without visible allergy. The type 2 endotype comprises; T helper type 2 (Th2) cells, type 2 innate lymphoid cells (ILC2), IgE-secreting B cells and eosinophils. Eosinophilic nonallergic asthma is ILC2 predominated, which produces IL-5 to recruit eosinophil into the mucosal airway. The second major subgroup of asthma is non-type 2 asthma, which contains heterogeneous group of endoypes and phenotypes, such as exercise-induced asthma, obesity induced asthma, etc. Neutrophilic asthma is not induced by allergens but can be induced by infections, cigarette smoke and pollution. IL-17 which is produced by Th17 cells and type 3 ILCs, can stimulate neutrophilic airway inflammation. Macrophages, dendritic cells and NKT cells are all capable of producing cytokines that are known to contribute in allergic and nonallergic asthma. Bronchial epithelial cell activation and release of cytokines, such as IL-33, IL-25 and TSLP play a major role in asthma. Especially, allergens or environmental exposure to toxic agents, such as pollutants, diesel exhaust, detergents may affect the epithelial barrier leading to asthma development. In this review, we focus on the immunologic mechanism of heterogenous asthma phenotypes.

摘要

哮喘是一种慢性气道疾病,影响着超过 3 亿人。哮喘的发病机制表现出明显的异质性,许多表型定义可见特征,而内型定义分子机制。随着新型生物疗法的发展,对常规哮喘治疗反应不佳的患者需要新型生物药物,如抗 IgE、抗 IL-5 和抗 IL4/IL13 来控制哮喘症状。医生越来越需要了解哮喘的免疫病理学,并对哮喘表型进行特征描述。哮喘与免疫系统激活、气道高反应性(AHR)、上皮细胞激活、黏液过度产生和气道重塑有关。固有免疫和适应性免疫都在哮喘的免疫机制中发挥作用。伴有嗜酸性粒细胞增多的 2 型哮喘是哮喘的一种常见表型。它既发生于有可见过敏的情况下,也发生于无可见过敏的情况下。2 型内型包括:辅助性 T 细胞 2(Th2)细胞、2 型先天淋巴细胞(ILC2)、分泌 IgE 的 B 细胞和嗜酸性粒细胞。非过敏性嗜酸性粒细胞性哮喘以 ILC2 为主导,其产生 IL-5 将嗜酸性粒细胞募集到黏膜气道中。哮喘的第二个主要亚组是非 2 型哮喘,它包含了异质性的内型和表型,如运动性哮喘、肥胖性哮喘等。中性粒细胞性哮喘不是由过敏原引起的,但可由感染、香烟烟雾和污染引起。Th17 细胞和 3 型 ILC 产生的 IL-17 可刺激中性粒细胞性气道炎症。巨噬细胞、树突状细胞和 NKT 细胞都能够产生细胞因子,这些细胞因子已知在过敏性和非过敏性哮喘中起作用。气道上皮细胞的激活和细胞因子的释放,如 IL-33、IL-25 和 TSLP,在哮喘中起主要作用。特别是过敏原或环境暴露于有毒物质,如污染物、柴油尾气、清洁剂,可能会影响上皮屏障,导致哮喘的发生。在这篇综述中,我们重点关注异质性哮喘表型的免疫机制。

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