Understanding the within-host dynamics of influenza A virus: from theory to clinical implications
Author(s) -
Christoforos Hadjichrysanthou,
Emilie Cauët,
Emma Lawrence,
Carolin Vegvari,
Frank de Wolf,
Roy M. Anderson
Publication year - 2016
Publication title -
journal of the royal society interface
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 139
eISSN - 1742-5689
pISSN - 1742-5662
DOI - 10.1098/rsif.2016.0289
Subject(s) - viral load , influenza a virus , oseltamivir , zanamivir , virus , dynamics (music) , virology , computer science , computational biology , biology , immunology , covid-19 , medicine , infectious disease (medical specialty) , physics , disease , pathology , acoustics
Mathematical models have provided important insights into acute viral dynamics within individual patients. In this paper, we study the simplest target cell-limited models to investigate the within-host dynamics of influenza A virus infection in humans. Despite the biological simplicity of the models, we show how these can be used to understand the severity of the infection and the key attributes of possible immunotherapy and antiviral drugs for the treatment of infection at different times post infection. Through an analytic approach, we derive and estimate simple summary biological quantities that can provide novel insights into the infection dynamics and the definition of clinical endpoints. We focus on nine quantities, including the area under the viral load curve, peak viral load, the time to peak viral load and the level of cell death due to infection. Using Markov chain Monte Carlo methods, we fitted the models to data collected from 12 untreated volunteers who participated in two clinical studies that tested the antiviral drugs oseltamivir and zanamivir. Based on the results, we also discuss various difficulties in deriving precise estimates of the parameters, even in the very simple models considered, when experimental data are limited to viral load measures and/or there is a limited number of viral load measurements post infection.
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