Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus

Background: It is unknown why human metapneumovirus (HMPV) and respiratory syncytial virus (RSV) cause severe respiratory infection in children, particularly in premature infants. Our aim was to investigate if there are defective airway antiviral responses to these viruses in young children with his...

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Autores:
Pancham, Krishna
Perez, Geovanny F.
Huseni, Shehlanoor
Jain, Amisha
Kurdi, Bassem
Rodriguez-Martinez, Carlos E.
Preciado, Diego
Rose, Mary C.
Nino, Gustavo
Tipo de recurso:
Article of journal
Fecha de publicación:
2015
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/3782
Acceso en línea:
http://hdl.handle.net/20.500.12495/3782
https://doi.org/10.1038/pr.2015.113
https://repositorio.unbosque.edu.co
Palabra clave:
Chemokine CCL5
Gestational age
Cross-sectional studies
Prospective studies
Rights
openAccess
License
Acceso abierto
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dc.title.spa.fl_str_mv Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
dc.title.translated.spa.fl_str_mv Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
title Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
spellingShingle Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
Chemokine CCL5
Gestational age
Cross-sectional studies
Prospective studies
title_short Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
title_full Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
title_fullStr Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
title_full_unstemmed Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
title_sort Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus
dc.creator.fl_str_mv Pancham, Krishna
Perez, Geovanny F.
Huseni, Shehlanoor
Jain, Amisha
Kurdi, Bassem
Rodriguez-Martinez, Carlos E.
Preciado, Diego
Rose, Mary C.
Nino, Gustavo
dc.contributor.author.none.fl_str_mv Pancham, Krishna
Perez, Geovanny F.
Huseni, Shehlanoor
Jain, Amisha
Kurdi, Bassem
Rodriguez-Martinez, Carlos E.
Preciado, Diego
Rose, Mary C.
Nino, Gustavo
dc.subject.keywords.spa.fl_str_mv Chemokine CCL5
Gestational age
Cross-sectional studies
Prospective studies
topic Chemokine CCL5
Gestational age
Cross-sectional studies
Prospective studies
description Background: It is unknown why human metapneumovirus (HMPV) and respiratory syncytial virus (RSV) cause severe respiratory infection in children, particularly in premature infants. Our aim was to investigate if there are defective airway antiviral responses to these viruses in young children with history of prematurity. Methods: Nasal airway secretions were collected from 140 children ≤3 y old without detectable virus (n = 80) or with PCR-confirmed HMPV or RSV infection (n = 60). Nasal protein levels of IFNγ, CCL5/RANTES, IL-10, IL-4, and IL-17 were determined using a multiplex magnetic bead immunoassay. Results: Full-term children with HMPV and RSV infection had increased levels of nasal airway IFNγ, CCL5, and IL-10 along with an elevation in Th1 (IFNγ)/Th2 (IL-4) ratios, which is expected during antiviral responses. In contrast, HMPV-infected premature children (< 32 wk gestation) did not exhibit increased Th1/Th2 ratios or elevated nasal airway secretion of IFNγ, CCL5, and IL-10 relative to uninfected controls. Conclusion: Our study is the first to demonstrate that premature infants have defective IFNγ, CCL5/RANTES, and IL-10 airway responses during HMPV infection and provides novel insights about the potential reason why HMPV causes severe respiratory disease in children with history of prematurity.
publishDate 2015
dc.date.issued.none.fl_str_mv 2015
dc.date.accessioned.none.fl_str_mv 2020-08-13T19:25:14Z
dc.date.available.none.fl_str_mv 2020-08-13T19:25:14Z
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dc.type.local.none.fl_str_mv Artículo de revista
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dc.identifier.issn.none.fl_str_mv 1530-0447
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12495/3782
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1038/pr.2015.113
dc.identifier.instname.spa.fl_str_mv instname:Universidad El Bosque
dc.identifier.reponame.spa.fl_str_mv reponame:Repositorio Institucional Universidad El Bosque
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identifier_str_mv 1530-0447
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url http://hdl.handle.net/20.500.12495/3782
https://doi.org/10.1038/pr.2015.113
https://repositorio.unbosque.edu.co
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartofseries.spa.fl_str_mv Pediatric Research, 1530-0447, Vol. 78, Nro. 4, 2015, p. 389-394
dc.relation.uri.none.fl_str_mv https://www.nature.com/articles/pr2015113
dc.rights.local.spa.fl_str_mv Acceso abierto
dc.rights.accessrights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
info:eu-repo/semantics/openAccess
Acceso abierto
dc.rights.creativecommons.none.fl_str_mv 2015-06-18
rights_invalid_str_mv Acceso abierto
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2015-06-18
eu_rights_str_mv openAccess
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dc.publisher.spa.fl_str_mv Springer Nature
dc.publisher.journal.spa.fl_str_mv Pediatric Research
institution Universidad El Bosque
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spelling Pancham, KrishnaPerez, Geovanny F.Huseni, ShehlanoorJain, AmishaKurdi, BassemRodriguez-Martinez, Carlos E.Preciado, DiegoRose, Mary C.Nino, Gustavo2020-08-13T19:25:14Z2020-08-13T19:25:14Z20151530-0447http://hdl.handle.net/20.500.12495/3782https://doi.org/10.1038/pr.2015.113instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquehttps://repositorio.unbosque.edu.coapplication/pdfengSpringer NaturePediatric ResearchPediatric Research, 1530-0447, Vol. 78, Nro. 4, 2015, p. 389-394https://www.nature.com/articles/pr2015113Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virusPremature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virusArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85Chemokine CCL5Gestational ageCross-sectional studiesProspective studiesBackground: It is unknown why human metapneumovirus (HMPV) and respiratory syncytial virus (RSV) cause severe respiratory infection in children, particularly in premature infants. Our aim was to investigate if there are defective airway antiviral responses to these viruses in young children with history of prematurity. Methods: Nasal airway secretions were collected from 140 children ≤3 y old without detectable virus (n = 80) or with PCR-confirmed HMPV or RSV infection (n = 60). Nasal protein levels of IFNγ, CCL5/RANTES, IL-10, IL-4, and IL-17 were determined using a multiplex magnetic bead immunoassay. Results: Full-term children with HMPV and RSV infection had increased levels of nasal airway IFNγ, CCL5, and IL-10 along with an elevation in Th1 (IFNγ)/Th2 (IL-4) ratios, which is expected during antiviral responses. In contrast, HMPV-infected premature children (< 32 wk gestation) did not exhibit increased Th1/Th2 ratios or elevated nasal airway secretion of IFNγ, CCL5, and IL-10 relative to uninfected controls. 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