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

被引:58
|
作者
Lee, Nelson [1 ,2 ]
Wong, Chun-Kwok [3 ]
Chan, Martin C. W. [4 ]
Yeung, Esther S. L. [1 ,3 ]
Tam, Wilson W. S. [5 ]
Tsang, Owen T. Y. [6 ]
Choi, Kin-Wing [7 ]
Chan, Paul K. S. [2 ,4 ]
Kwok, Angela [4 ]
Lui, Grace C. Y. [1 ]
Leung, Wai-Shing [6 ]
Yung, Irene M. H. [1 ]
Wong, Rity Y. K. [1 ,6 ]
Cheung, Catherine S. K. [1 ]
Hui, David S. C. [1 ,2 ]
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, 9-F Lui Che Woo Clin Sci Bldg, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Stanley Ho Ctr Emerging Infect Dis, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Dept Chem Pathol, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
[5] Natl Univ Singapore, Alice Lee Ctr Nursing Studies, Singapore, Singapore
[6] Princess Margaret Hosp, Dept Med & Geriatr, Hong Kong, Hong Kong, Peoples R China
[7] Alice Ho Miu Ling Nethersole Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
关键词
Macrolide; Anti-inflammatory effects; Influenza; CLARITHROMYCIN; AZITHROMYCIN; VIRUS; HYPERCYTOKINEMIA; MECHANISMS; MANAGEMENT; MORTALITY; INFECTION; SURVIVAL; REGIMENS;
D O I
10.1016/j.antiviral.2017.05.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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: beta -0.037, 95%CI-0.067,-0.007, P = 0.016; reduction from baseline -83.4% vs -59.5%), CXCL8/IL-8 (beta -0.018, 95%CI-0.037,0.000, P = 0.056; -80.5% vs -58.0%), IL-17 (beta -0.064, 95%CI-0.117,-0.012, P = 0.015; -74.0% vs -34.3%), CXCL9/MIG (beta -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 (beta -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. Copyright (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:48 / 56
页数:9
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