低剂量、长期大环内酯治疗哮喘:综述。

Q2 Medicine
Umur Hatipoglu, Israel Rubinstein
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引用次数: 12

摘要

大环内酯类药物是50多年前从链霉菌中分离出来的一类抗菌素,广泛用于治疗人类肺部感染。此外,越来越多的实验和临床证据表明,长期(年)、低剂量(亚抗菌)的14和15元环大环内酯类抗生素,如红霉素、克拉霉素、罗红霉素和阿奇霉素,表现出与其抗感染特性不同的免疫调节和组织修复作用。这些有益的作用适用于各种肺部疾病,包括弥漫性泛细支气管炎、囊性纤维化、持续性慢性鼻窦炎、鼻息肉病、支气管扩张、哮喘和隐源性组织性肺炎。本综述的目的是概述大环内酯类抗生素对哮喘患者的免疫调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-dose, long-term macrolide therapy in asthma: An overview.

Macrolides, a class of antimicrobials isolated from Streptomycetes more than 50 years ago, are used extensively to treat sinopulmonary infections in humans. In addition, a growing body of experimental and clinical evidence indicates that long-term (years), low (sub-antimicrobial)-dose 14- and 15-membered ring macrolide antibiotics, such as erythromycin, clarithromycin, roxithromycin and azithromycin, express immunomodulatory and tissue reparative effects that are distinct from their anti-infective properties. These salutary effects are operative in various lung disorders, including diffuse panbronchiolitis, cystic fibrosis, persistent chronic rhinosinusitis, nasal polyposis, bronchiectasis, asthma and cryptogenic organizing pneumonia.The purpose of this overview is to outline the immunomodulatory effects of macrolide antibiotics in patients with asthma.

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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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