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Innate Immunity and the Inter-exposure Interval Determine the Dynamics of Secondary Influenza Virus Infection and Explain Observed Viral Hierarchies

Influenza is an infectious disease that primarily attacks the respiratory system. Innate immunity provides both a very early defense to influenza virus invasion and an effective control of viral growth. Previous modelling studies of virus–innate immune response interactions have focused on infection...

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Autores principales: Cao, Pengxing, Yan, Ada W. C., Heffernan, Jane M., Petrie, Stephen, Moss, Robert G., Carolan, Louise A., Guarnaccia, Teagan A., Kelso, Anne, Barr, Ian G., McVernon, Jodie, Laurie, Karen L., McCaw, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540579/
https://www.ncbi.nlm.nih.gov/pubmed/26284917
http://dx.doi.org/10.1371/journal.pcbi.1004334
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author Cao, Pengxing
Yan, Ada W. C.
Heffernan, Jane M.
Petrie, Stephen
Moss, Robert G.
Carolan, Louise A.
Guarnaccia, Teagan A.
Kelso, Anne
Barr, Ian G.
McVernon, Jodie
Laurie, Karen L.
McCaw, James M.
author_facet Cao, Pengxing
Yan, Ada W. C.
Heffernan, Jane M.
Petrie, Stephen
Moss, Robert G.
Carolan, Louise A.
Guarnaccia, Teagan A.
Kelso, Anne
Barr, Ian G.
McVernon, Jodie
Laurie, Karen L.
McCaw, James M.
author_sort Cao, Pengxing
collection PubMed
description Influenza is an infectious disease that primarily attacks the respiratory system. Innate immunity provides both a very early defense to influenza virus invasion and an effective control of viral growth. Previous modelling studies of virus–innate immune response interactions have focused on infection with a single virus and, while improving our understanding of viral and immune dynamics, have been unable to effectively evaluate the relative feasibility of different hypothesised mechanisms of antiviral immunity. In recent experiments, we have applied consecutive exposures to different virus strains in a ferret model, and demonstrated that viruses differed in their ability to induce a state of temporary immunity or viral interference capable of modifying the infection kinetics of the subsequent exposure. These results imply that virus-induced early immune responses may be responsible for the observed viral hierarchy. Here we introduce and analyse a family of within-host models of re-infection viral kinetics which allow for different viruses to stimulate the innate immune response to different degrees. The proposed models differ in their hypothesised mechanisms of action of the non-specific innate immune response. We compare these alternative models in terms of their abilities to reproduce the re-exposure data. Our results show that 1) a model with viral control mediated solely by a virus-resistant state, as commonly considered in the literature, is not able to reproduce the observed viral hierarchy; 2) the synchronised and desynchronised behaviour of consecutive virus infections is highly dependent upon the interval between primary virus and challenge virus exposures and is consistent with virus-dependent stimulation of the innate immune response. Our study provides the first mechanistic explanation for the recently observed influenza viral hierarchies and demonstrates the importance of understanding the host response to multi-strain viral infections. Re-exposure experiments provide a new paradigm in which to study the immune response to influenza and its role in viral control.
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spelling pubmed-45405792015-08-24 Innate Immunity and the Inter-exposure Interval Determine the Dynamics of Secondary Influenza Virus Infection and Explain Observed Viral Hierarchies Cao, Pengxing Yan, Ada W. C. Heffernan, Jane M. Petrie, Stephen Moss, Robert G. Carolan, Louise A. Guarnaccia, Teagan A. Kelso, Anne Barr, Ian G. McVernon, Jodie Laurie, Karen L. McCaw, James M. PLoS Comput Biol Research Article Influenza is an infectious disease that primarily attacks the respiratory system. Innate immunity provides both a very early defense to influenza virus invasion and an effective control of viral growth. Previous modelling studies of virus–innate immune response interactions have focused on infection with a single virus and, while improving our understanding of viral and immune dynamics, have been unable to effectively evaluate the relative feasibility of different hypothesised mechanisms of antiviral immunity. In recent experiments, we have applied consecutive exposures to different virus strains in a ferret model, and demonstrated that viruses differed in their ability to induce a state of temporary immunity or viral interference capable of modifying the infection kinetics of the subsequent exposure. These results imply that virus-induced early immune responses may be responsible for the observed viral hierarchy. Here we introduce and analyse a family of within-host models of re-infection viral kinetics which allow for different viruses to stimulate the innate immune response to different degrees. The proposed models differ in their hypothesised mechanisms of action of the non-specific innate immune response. We compare these alternative models in terms of their abilities to reproduce the re-exposure data. Our results show that 1) a model with viral control mediated solely by a virus-resistant state, as commonly considered in the literature, is not able to reproduce the observed viral hierarchy; 2) the synchronised and desynchronised behaviour of consecutive virus infections is highly dependent upon the interval between primary virus and challenge virus exposures and is consistent with virus-dependent stimulation of the innate immune response. Our study provides the first mechanistic explanation for the recently observed influenza viral hierarchies and demonstrates the importance of understanding the host response to multi-strain viral infections. Re-exposure experiments provide a new paradigm in which to study the immune response to influenza and its role in viral control. Public Library of Science 2015-08-18 /pmc/articles/PMC4540579/ /pubmed/26284917 http://dx.doi.org/10.1371/journal.pcbi.1004334 Text en © 2015 Cao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cao, Pengxing
Yan, Ada W. C.
Heffernan, Jane M.
Petrie, Stephen
Moss, Robert G.
Carolan, Louise A.
Guarnaccia, Teagan A.
Kelso, Anne
Barr, Ian G.
McVernon, Jodie
Laurie, Karen L.
McCaw, James M.
Innate Immunity and the Inter-exposure Interval Determine the Dynamics of Secondary Influenza Virus Infection and Explain Observed Viral Hierarchies
title Innate Immunity and the Inter-exposure Interval Determine the Dynamics of Secondary Influenza Virus Infection and Explain Observed Viral Hierarchies
title_full Innate Immunity and the Inter-exposure Interval Determine the Dynamics of Secondary Influenza Virus Infection and Explain Observed Viral Hierarchies
title_fullStr Innate Immunity and the Inter-exposure Interval Determine the Dynamics of Secondary Influenza Virus Infection and Explain Observed Viral Hierarchies
title_full_unstemmed Innate Immunity and the Inter-exposure Interval Determine the Dynamics of Secondary Influenza Virus Infection and Explain Observed Viral Hierarchies
title_short Innate Immunity and the Inter-exposure Interval Determine the Dynamics of Secondary Influenza Virus Infection and Explain Observed Viral Hierarchies
title_sort innate immunity and the inter-exposure interval determine the dynamics of secondary influenza virus infection and explain observed viral hierarchies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540579/
https://www.ncbi.nlm.nih.gov/pubmed/26284917
http://dx.doi.org/10.1371/journal.pcbi.1004334
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