Modeling within-host dynamics of influenza virus infection including immune responses.

Influenza virus infection remains a public health problem worldwide. The mechanisms underlying viral control during an uncomplicated influenza virus infection are not fully understood. Here, we developed a mathematical model including both innate and adaptive immune responses to study the within-hos...

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Main Authors: Kasia A Pawelek, Giao T Huynh, Michelle Quinlivan, Ann Cullinane, Libin Rong, Alan S Perelson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC3386161?pdf=render
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spelling doaj-83e9e376327243d8bdfc6cff4f7cc01f2020-11-24T21:56:05ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582012-01-0186e100258810.1371/journal.pcbi.1002588Modeling within-host dynamics of influenza virus infection including immune responses.Kasia A PawelekGiao T HuynhMichelle QuinlivanAnn CullinaneLibin RongAlan S PerelsonInfluenza virus infection remains a public health problem worldwide. The mechanisms underlying viral control during an uncomplicated influenza virus infection are not fully understood. Here, we developed a mathematical model including both innate and adaptive immune responses to study the within-host dynamics of equine influenza virus infection in horses. By comparing modeling predictions with both interferon and viral kinetic data, we examined the relative roles of target cell availability, and innate and adaptive immune responses in controlling the virus. Our results show that the rapid and substantial viral decline (about 2 to 4 logs within 1 day) after the peak can be explained by the killing of infected cells mediated by interferon activated cells, such as natural killer cells, during the innate immune response. After the viral load declines to a lower level, the loss of interferon-induced antiviral effect and an increased availability of target cells due to loss of the antiviral state can explain the observed short phase of viral plateau in which the viral level remains unchanged or even experiences a minor second peak in some animals. An adaptive immune response is needed in our model to explain the eventual viral clearance. This study provides a quantitative understanding of the biological factors that can explain the viral and interferon kinetics during a typical influenza virus infection.http://europepmc.org/articles/PMC3386161?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kasia A Pawelek
Giao T Huynh
Michelle Quinlivan
Ann Cullinane
Libin Rong
Alan S Perelson
spellingShingle Kasia A Pawelek
Giao T Huynh
Michelle Quinlivan
Ann Cullinane
Libin Rong
Alan S Perelson
Modeling within-host dynamics of influenza virus infection including immune responses.
PLoS Computational Biology
author_facet Kasia A Pawelek
Giao T Huynh
Michelle Quinlivan
Ann Cullinane
Libin Rong
Alan S Perelson
author_sort Kasia A Pawelek
title Modeling within-host dynamics of influenza virus infection including immune responses.
title_short Modeling within-host dynamics of influenza virus infection including immune responses.
title_full Modeling within-host dynamics of influenza virus infection including immune responses.
title_fullStr Modeling within-host dynamics of influenza virus infection including immune responses.
title_full_unstemmed Modeling within-host dynamics of influenza virus infection including immune responses.
title_sort modeling within-host dynamics of influenza virus infection including immune responses.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2012-01-01
description Influenza virus infection remains a public health problem worldwide. The mechanisms underlying viral control during an uncomplicated influenza virus infection are not fully understood. Here, we developed a mathematical model including both innate and adaptive immune responses to study the within-host dynamics of equine influenza virus infection in horses. By comparing modeling predictions with both interferon and viral kinetic data, we examined the relative roles of target cell availability, and innate and adaptive immune responses in controlling the virus. Our results show that the rapid and substantial viral decline (about 2 to 4 logs within 1 day) after the peak can be explained by the killing of infected cells mediated by interferon activated cells, such as natural killer cells, during the innate immune response. After the viral load declines to a lower level, the loss of interferon-induced antiviral effect and an increased availability of target cells due to loss of the antiviral state can explain the observed short phase of viral plateau in which the viral level remains unchanged or even experiences a minor second peak in some animals. An adaptive immune response is needed in our model to explain the eventual viral clearance. This study provides a quantitative understanding of the biological factors that can explain the viral and interferon kinetics during a typical influenza virus infection.
url http://europepmc.org/articles/PMC3386161?pdf=render
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