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辅助大环内酯类药物治疗对住院流感成人的抗炎作用:一项随机对照试验。

Anti-inflammatory effects of adjunctive macrolide treatment in adults hospitalized with influenza: A randomized controlled trial.

机构信息

Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong; Stanley Ho Center for Emerging Infectious Diseases, The Chinese University of Hong Kong, Hong Kong.

Department of Chemical Pathology, The Chinese University of Hong Kong, Hong Kong.

出版信息

Antiviral Res. 2017 Aug;144:48-56. doi: 10.1016/j.antiviral.2017.05.008. Epub 2017 May 20.

Abstract

INTRODUCTION

  • Macrolides can ameliorate inflammation in respiratory diseases, providing clinical benefits. Data in influenza is lacking.

METHOD

  • A randomized, open-label, multicenter trial among adults hospitalized for laboratory-confirmed influenza was conducted. Study treatments of oseltamivir and azithromycin (500 mg/day), or oseltamivir alone, both for 5 days, were allocated at 1:1 ratio. The primary outcome was plasma cytokine/chemokine concentration change over time (Day 0-10); secondary outcomes were viral load and symptom score changes. Generalized Estimating Equation (GEE) models were used to analyze longitudinal data.

RESULTS

  • Fifty patients were randomized to the oseltamivir-azithromycin or oseltamivir groups, with comparable baseline characteristics (age, 57 ± 18 years; A/H3N2, 70%), complications (72%), and viral load. Pro-inflammatory cytokines IL-6 (GEE: β -0.037, 95%CI-0.067,-0.007, P = 0.016; reduction from baseline -83.4% vs -59.5%), CXCL8/IL-8 (β -0.018, 95%CI-0.037,0.000, P = 0.056; -80.5% vs -58.0%), IL-17 (β -0.064, 95%CI-0.117,-0.012, P = 0.015; -74.0% vs -34.3%), CXCL9/MIG (β -0.010, 95%CI-0.020,0.000, P = 0.043; -71.3% vs -56.0%), sTNFR-1, IL-18, and CRP declined faster in the oseltamivir-azithromycin group. There was a trend toward faster symptom resolution (β -0.463, 95%CI-1.297,0.371). Viral RNA decline (P = 0.777) and culture-negativity rates were unaffected. Additional ex vivo studies confirmed reduced induction of IL-6 (P = 0.017) and CXCL8/IL-8 (P = 0.005) with azithromycin.

CONCLUSION

  • We found significant anti-inflammatory effects with adjunctive macrolide treatment in adults with severe influenza infections. Virus control was unimpaired. Clinical benefits of a macrolide-containing regimen deserve further study. [ClinicalTrials.gov NCT01779570].
摘要

简介

  • 大环内酯类药物可改善呼吸道疾病的炎症,提供临床获益。流感方面的数据尚缺乏。

方法

  • 这是一项在因实验室确诊流感而住院的成年人中开展的随机、开放标签、多中心试验。奥司他韦和阿奇霉素(500mg/天)或奥司他韦单药治疗,均持续 5 天,以 1:1 的比例进行分配。主要结局为血浆细胞因子/趋化因子浓度随时间的变化(第 0-10 天);次要结局为病毒载量和症状评分的变化。使用广义估计方程(GEE)模型分析纵向数据。

结果

  • 50 例患者被随机分配至奥司他韦-阿奇霉素或奥司他韦组,两组具有可比的基线特征(年龄,57±18 岁;A/H3N2,70%)、并发症(72%)和病毒载量。促炎细胞因子 IL-6(GEE:β-0.037,95%CI-0.067,-0.007,P=0.016;与基线相比的降低幅度-83.4% vs-59.5%)、CXCL8/IL-8(β-0.018,95%CI-0.037,0.000,P=0.056;-80.5% vs-58.0%)、IL-17(β-0.064,95%CI-0.117,-0.012,P=0.015;-74.0% vs-34.3%)、CXCL9/MIG(β-0.010,95%CI-0.020,0.000,P=0.043;-71.3% vs-56.0%)、sTNFR-1、IL-18 和 CRP 在奥司他韦-阿奇霉素组中下降更快。症状缓解更快(β-0.463,95%CI-1.297,0.371),这一趋势具有统计学意义。病毒 RNA 下降(P=0.777)和培养阴性率不受影响。额外的离体研究证实,阿奇霉素可降低 IL-6(P=0.017)和 CXCL8/IL-8(P=0.005)的诱导。

结论

  • 我们发现,在患有严重流感感染的成年人中,大环内酯类药物辅助治疗具有显著的抗炎作用。病毒控制不受影响。含有大环内酯类药物的治疗方案的临床获益值得进一步研究。[临床试验.gov NCT01779570]。

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