Neuraminidase inhibitors for treatment of human and avian strain influenza: A comparative modeling study

被引:40
作者
Dobrovolny, Hana M. [1 ]
Gieschke, Ronald [2 ]
Davies, Brian E. [3 ]
Jumbe, Nelson L. [2 ]
Beauchemin, Catherine A. A. [1 ]
机构
[1] Ryerson Univ, Dept Phys, Toronto, ON, Canada
[2] F Hoffmann La Roche & Co Ltd, Basel, Switzerland
[3] F Hoffmann La Roche Inc, Nutley, NJ USA
基金
加拿大自然科学与工程研究理事会;
关键词
Avian influenza; Neuraminidase inhibitor; Mathematical modeling; Antiviral treatment; Infectious disease; H5N1; VIRUS; HUMAN INFECTION; INTRAVENOUS ZANAMIVIR; CYTOKINE RESPONSES; EPITHELIAL-CELLS; IMMUNE-RESPONSE; OSELTAMIVIR; RESISTANCE; EFFICACY; RECEPTOR;
D O I
10.1016/j.jtbi.2010.10.017
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Treatment of seasonal influenza viral infections using antivirals such as neuraminidase inhibitors (NAIs) has been proven effective if administered within 48 h post-infection. However, there is growing evidence that antiviral treatment of infections with avian-derived strains even as late as 6 days post-infection (dpi) can significantly reduce infection severity and duration. Using a mathematical model of in-host influenza viral infections which can capture the kinetics of both a short-lived, typical, seasonal infection and a severe infection exhibiting sustained viral titer, we explore differences in the effects of NAI treatment on both types of influenza viral infections. Comparison of our model's behavior against experimental data from patients naturally infected with avian strains yields estimates for the times at which patients were infected that are consistent with those reported by the patients, and estimates of drug efficacies that are lower for patients who died than for those who recovered. In addition, our model suggests that the sustained, high, viral titers often seen in more severe influenza virus infections are the reason why antiviral treatment delayed by as much as 6 dpi will still lead to reduced viral titers and shortened illness. We conclude that NAIs may be an effective and beneficial treatment strategy against more severe strains of influenza virus characterized by high, sustained, viral titers. We believe that our mathematical model will be an effective tool in guiding treatment of severe influenza viral infections with antivirals. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:234 / 244
页数:11
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