Host susceptibility to severe influenza A virus infection

Abstract Most people exposed to a new flu virus do not notice any symptoms. A small minority develops critical illness. Some of this extremely broad variation in susceptibility is explained by the size of the initial inoculum or the influenza exposure history of the individual; some is explained by...

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Main Authors: Sara Clohisey, John Kenneth Baillie
Format: Article
Language:English
Published: BMC 2019-09-01
Series:Critical Care
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13054-019-2566-7
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spelling doaj-55a1078a8bf345298a05466dddfa486d2020-11-25T02:25:03ZengBMCCritical Care1364-85352019-09-0123111010.1186/s13054-019-2566-7Host susceptibility to severe influenza A virus infectionSara Clohisey0John Kenneth Baillie1Division of Genetics and Genomics, Roslin Institute, University of Edinburgh, Easter BushDivision of Genetics and Genomics, Roslin Institute, University of Edinburgh, Easter BushAbstract Most people exposed to a new flu virus do not notice any symptoms. A small minority develops critical illness. Some of this extremely broad variation in susceptibility is explained by the size of the initial inoculum or the influenza exposure history of the individual; some is explained by generic host factors, such as frailty, that decrease resilience following any systemic insult. Some demographic factors (pregnancy, obesity, and advanced age) appear to confer a more specific susceptibility to severe illness following infection with influenza viruses. As with other infectious diseases, a substantial component of susceptibility is determined by host genetics. Several genetic susceptibility variants have now been reported with varying levels of evidence. Susceptible hosts may have impaired intracellular controls of viral replication (e.g. IFITM3, TMPRS22 variants), defective interferon responses (e.g. GLDC, IRF7/9 variants), or defects in cell-mediated immunity with increased baseline levels of systemic inflammation (obesity, pregnancy, advanced age). These mechanisms may explain the prolonged viral replication reported in critically ill patients with influenza: patients with life-threatening disease are, by definition, abnormal hosts. Understanding these molecular mechanisms of susceptibility may in the future enable the design of host-directed therapies to promote resilience.http://link.springer.com/article/10.1186/s13054-019-2566-7InfluenzaARDSSusceptibilityGenetics
collection DOAJ
language English
format Article
sources DOAJ
author Sara Clohisey
John Kenneth Baillie
spellingShingle Sara Clohisey
John Kenneth Baillie
Host susceptibility to severe influenza A virus infection
Critical Care
Influenza
ARDS
Susceptibility
Genetics
author_facet Sara Clohisey
John Kenneth Baillie
author_sort Sara Clohisey
title Host susceptibility to severe influenza A virus infection
title_short Host susceptibility to severe influenza A virus infection
title_full Host susceptibility to severe influenza A virus infection
title_fullStr Host susceptibility to severe influenza A virus infection
title_full_unstemmed Host susceptibility to severe influenza A virus infection
title_sort host susceptibility to severe influenza a virus infection
publisher BMC
series Critical Care
issn 1364-8535
publishDate 2019-09-01
description Abstract Most people exposed to a new flu virus do not notice any symptoms. A small minority develops critical illness. Some of this extremely broad variation in susceptibility is explained by the size of the initial inoculum or the influenza exposure history of the individual; some is explained by generic host factors, such as frailty, that decrease resilience following any systemic insult. Some demographic factors (pregnancy, obesity, and advanced age) appear to confer a more specific susceptibility to severe illness following infection with influenza viruses. As with other infectious diseases, a substantial component of susceptibility is determined by host genetics. Several genetic susceptibility variants have now been reported with varying levels of evidence. Susceptible hosts may have impaired intracellular controls of viral replication (e.g. IFITM3, TMPRS22 variants), defective interferon responses (e.g. GLDC, IRF7/9 variants), or defects in cell-mediated immunity with increased baseline levels of systemic inflammation (obesity, pregnancy, advanced age). These mechanisms may explain the prolonged viral replication reported in critically ill patients with influenza: patients with life-threatening disease are, by definition, abnormal hosts. Understanding these molecular mechanisms of susceptibility may in the future enable the design of host-directed therapies to promote resilience.
topic Influenza
ARDS
Susceptibility
Genetics
url http://link.springer.com/article/10.1186/s13054-019-2566-7
work_keys_str_mv AT saraclohisey hostsusceptibilitytosevereinfluenzaavirusinfection
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