Simpson Jodie L, Powell Heather, Boyle Michael J, Scott Rodney J, Gibson Peter G
NHMRC Centre for Respiratory and Sleep Medicine, School of Medicine and Public Health, University of Newcastle, Callaghan, Australia.
Am J Respir Crit Care Med. 2008 Jan 15;177(2):148-55. doi: 10.1164/rccm.200707-1134OC. Epub 2007 Oct 18.
Patients with refractory asthma have persistent symptoms despite maximal treatment with inhaled corticosteroids and long-acting bronchodilators. The availability of add-on therapies is limited, and effective add-on therapies that target noneosinophilic airway inflammation are needed. Macrolide antibiotics, such as clarithromycin, have in vitro efficacy against IL-8 and neutrophils, key inflammatory mediators in noneosinophilic asthma.
To determine the efficacy of clarithromycin in patients with severe refractory asthma and specifically in a subgroup of patients with noneosinophilic asthma.
Subjects with severe refractory asthma (n = 45) were randomized to receive clarithromycin (500 mg twice daily) or placebo for 8 weeks.
The primary outcome for this study was sputum IL-8 concentration. Other inflammatory outcomes assessed included sputum neutrophil numbers and concentrations of neutrophil elastase and matrix metalloproteinase (MMP)-9. Clinical outcomes were also assessed, including lung function, airway hyperresponsiveness to hypertonic saline, asthma control, quality of life, and symptoms. Clarithromycin therapy significantly reduced airway concentrations of IL-8 and neutrophil numbers and improved quality-of-life scores compared with placebo. Reductions in neutrophil elastase and MMP-9 concentrations were also observed. These reductions in inflammation were most marked in those with refractory noneosinophilic asthma.
Clarithromycin therapy can modulate IL-8 levels and neutrophil accumulation and activation in the airways of patients with refractory asthma. Macrolide therapy may be an important additional therapy that could be used to reduce noneosinophilic airway inflammation, particularly neutrophilic inflammation, in asthma. Clinical trial registered with the Australian Clinical Trials Registry www.actr.org.au (No. 12605000318684).
尽管使用吸入性糖皮质激素和长效支气管扩张剂进行了最大程度的治疗,难治性哮喘患者仍有持续症状。附加治疗方法有限,因此需要针对非嗜酸性粒细胞性气道炎症的有效附加治疗方法。大环内酯类抗生素,如克拉霉素,在体外对白细胞介素-8(IL-8)和中性粒细胞具有疗效,而白细胞介素-8和中性粒细胞是非嗜酸性粒细胞性哮喘中的关键炎症介质。
确定克拉霉素对重度难治性哮喘患者,特别是对非嗜酸性粒细胞性哮喘亚组患者的疗效。
将重度难治性哮喘患者(n = 45)随机分为两组,分别接受克拉霉素(每日两次,每次500毫克)或安慰剂治疗,为期8周。
本研究的主要结局指标是痰液中IL-8浓度。评估的其他炎症结局指标包括痰液中性粒细胞数量以及中性粒细胞弹性蛋白酶和基质金属蛋白酶(MMP)-9的浓度。还评估了临床结局,包括肺功能、气道对高渗盐水的高反应性、哮喘控制情况、生活质量和症状。与安慰剂相比,克拉霉素治疗可显著降低气道中IL-8浓度和中性粒细胞数量,并改善生活质量评分。还观察到中性粒细胞弹性蛋白酶和MMP-9浓度降低。这些炎症指标的降低在难治性非嗜酸性粒细胞性哮喘患者中最为明显。
克拉霉素治疗可调节难治性哮喘患者气道中的IL-8水平以及中性粒细胞的聚集和激活。大环内酯类药物治疗可能是一种重要的附加治疗方法,可用于减轻哮喘中的非嗜酸性粒细胞性气道炎症,尤其是中性粒细胞炎症。该临床试验已在澳大利亚临床试验注册中心(www.actr.org.au)注册(注册号:12605000318684)。