The Mechanisms for Within-Host Influenza Virus Control Affect Model-Based Assessment and Prediction of Antiviral Treatment

被引:24
作者
Cao, Pengxing [1 ]
McCaw, James M. [1 ,2 ,3 ]
机构
[1] Univ Melbourne, Sch Math & Stat, Melbourne, Vic 3010, Australia
[2] Univ Melbourne, Melbourne Sch Populat & Global Hlth, Ctr Epidemiol & Biostat, Melbourne, Vic 3010, Australia
[3] Royal Childrens Hosp, Murdoch Childrens Res Inst, Infect & Immun Theme, Modelling & Simulat, Parkville, Vic 3052, Australia
来源
VIRUSES-BASEL | 2017年 / 9卷 / 08期
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
model selection; target cell depletion; immune response; neuraminidase inhibitor; drug efficacy; ADAPTIVE IMMUNE-RESPONSE; A-VIRUS; NEURAMINIDASE INHIBITORS; MATHEMATICAL-MODEL; PUBLIC-HEALTH; HIGH-RISK; T-CELLS; INFECTION; OSELTAMIVIR; DYNAMICS;
D O I
10.3390/v9080197
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Models of within-host influenza viral dynamics have contributed to an improved understanding of viral dynamics and antiviral effects over the past decade. Existing models can be classified into two broad types based on the mechanism of viral control: models utilising target cell depletion to limit the progress of infection and models which rely on timely activation of innate and adaptive immune responses to control the infection. In this paper, we compare how two exemplar models based on these different mechanisms behave and investigate how the mechanistic difference affects the assessment and prediction of antiviral treatment. We find that the assumed mechanism for viral control strongly influences the predicted outcomes of treatment. Furthermore, we observe that for the target cell-limited model the assumed drug efficacy strongly influences the predicted treatment outcomes. The area under the viral load curve is identified as the most reliable predictor of drug efficacy, and is robust to model selection. Moreover, with support from previous clinical studies, we suggest that the target cell-limited model is more suitable for modelling in vitro assays or infection in some immunocompromised/immunosuppressed patients while the immune response model is preferred for predicting the infection/antiviral effect in immunocompetent animals/patients.
引用
收藏
页数:20
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