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鼻息肉和阿司匹林加重的呼吸道疾病。

Nasal Polyposis and Aspirin-Exacerbated Respiratory Disease.

机构信息

Allergy-Immunology, Scripps Health, San Diego, CA, USA; Scripps Clinic Carmel Valley, 3811 Valley Centre Drive, San Diego, CA 92130, USA.

Allergy-Immunology, Scripps Health, San Diego, CA, USA; Scripps Clinic Carmel Valley, 3811 Valley Centre Drive, San Diego, CA 92130, USA.

出版信息

Immunol Allergy Clin North Am. 2020 May;40(2):329-343. doi: 10.1016/j.iac.2019.12.002. Epub 2020 Jan 27.

Abstract

Aspirin-exacerbated respiratory disease (AERD) is characterized by eosinophilic chronic rhinosinusitis with nasal polyps, asthma, and upper-/lower-respiratory tract reactions to nonsteroidal antiinflammatory drugs. Persistent, severe disease, anosmia, and alcohol sensitivity is typical. AERD is mediated by multiple pathways, including aberrant arachidonic acid metabolism leading to elevated leukotriene E4 and decreased prostaglandin E2. Mast cell mediators (prostaglandin D2) and unique properties of eosinophils and type 2 innate lymphoid cells, along with receptor-mediated signaling, also contribute to AERD pathogenesis. Pharmacologic therapies are a cornerstone of AERD treatment and include leukotriene modifiers, corticosteroids, biologics, and aspirin.

摘要

阿司匹林加重性呼吸系统疾病(AERD)的特征是伴鼻息肉的嗜酸性慢性鼻-鼻窦炎、哮喘,以及对上/下呼吸道对非甾体抗炎药的反应。持续性、严重疾病、嗅觉缺失和酒精敏感性是其典型特征。AERD 是由多种途径介导的,包括异常的花生四烯酸代谢导致白三烯 E4 升高和前列腺素 E2 降低。肥大细胞介质(前列腺素 D2)和嗜酸性粒细胞和 2 型先天淋巴细胞的独特特性,以及受体介导的信号转导,也有助于 AERD 的发病机制。药物治疗是 AERD 治疗的基石,包括白三烯调节剂、皮质类固醇、生物制剂和阿司匹林。

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