大环内酯类药物在囊性纤维化中的作用?

Joanne M Wolter, Sharon L Seeney, Joseph G McCormack
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引用次数: 8

摘要

一系列抗炎特性,对亚抑制浓度的铜绿假单胞菌具有抗感染作用的证据,以及弥漫性泛细支气管炎(一种与囊性纤维化(CF)共同特征的疾病)患者的积极临床经验,促使研究评估大环内酯类药物在CF患者中的作用。新的大环内酯类药物如阿奇霉素具有耐受性改善和细胞内半衰期延长的优点,需要不频繁的给药方案。最初的研究结果表明,对CF患者进行几个月的大环内酯治疗有益。肺功能的改善最初是在一项针对儿童的小型开放研究中显示的,而与安慰剂相比,肺功能的维持、急性呼吸恶化的减少和系统性炎症标志物的减少在一项随机、成年CF患者大环内酯类药物治疗的安慰剂对照研究。需要额外的对照研究来确定最佳药物、剂量、治疗时间以及CF患者长期使用大环内酯类药物治疗的长期不良反应。长期使用大环内酯类药物诱导对其他上呼吸道细菌(如肺炎球菌)的耐药性的潜力尚未探索。从CF患者的痰中测量细胞因子和炎症介质在技术上是困难的,并且与疾病活动无关。对于CF新疗法的评估,需要易于测量、可重复且具有临床意义的终点。除了肺功能外,选择合适的结局指标在确定大环内酯类药物对CF患者的疗效的临床试验中,需要仔细考虑疾病活动的监测。尽管大环内酯类药物已经在一些中心被规定为长期使用,但大环内酯类药物在CF治疗中使用的循证建议预计在几年内不会出现。需要进一步研究大环内酯类药物在CF患者肺部的抗炎作用机制,以及这种治疗是否长期有益。
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Macrolides in cystic fibrosis: is there a role?

A spectrum of anti-inflammatory properties, evidence of anti-infective action against Pseudomonas aeruginosa at sub-inhibitory concentrations and positive clinical experience in patients with diffuse panbronchiolitis, a disease with features in common with cystic fibrosis (CF), has prompted research to evaluate the role of macrolide therapy in patients with CF. Newer macrolides such as azithromycin have the advantage of improved tolerability and a prolonged intracellular half-life requiring an infrequent dosing regimen. Results from initial studies suggest a benefit from several months of macrolide therapy in patients with CF. An improvement in lung function was initially shown in a small open study in children, while maintenance of lung function compared with placebo, reduced acute respiratory exacerbations, and reduced systemic markers of inflammation were demonstrated in a randomized, placebo-controlled study of macrolide therapy in adult patients with CF. Additional controlled studies are required to determine optimal drug, dosage, and duration of therapy, and long-term adverse effects of prolonged therapy with macrolides in patients with CF. The potential, with long-term use, to induce resistance against other bacteria colonizing the upper respiratory tract e.g. pneumococci has not been explored. Measurement of cytokines and inflammatory mediators from the sputum of patients with CF is technically difficult and does not correlate with disease activity. There is a need for easily measurable, reproducible and clinically meaningful end-points for evaluation of new therapies in CF. The choice of appropriate outcome measures, apart from lung function, to monitor disease activity needs careful consideration in clinical trials determining the efficacy of macrolides in patients with CF. Evidence-based recommendations for the use of macrolides in the treatment of CF are not expected for some years although macrolides are already being prescribed for long-term use in some centers. There is a need for further research into mechanisms of anti-inflammatory action of macrolides in the lungs of patients with CF and whether or not such therapy may be beneficial in the long term.

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