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About:
Exacerbated Innate Host Response to SARS-CoV in Aged Non-Human Primates
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schema:ScholarlyArticle
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Exacerbated Innate Host Response to SARS-CoV in Aged Non-Human Primates
Creator
Kuiken, Thijs
Osterhaus, Albert
Andeweg, Arno
Haagmans, Bart
De Lang, Anna
Eijkemans, Marinus
Leijten, Lonneke
Smits, Saskia
Van Amerongen, Geert
Van Den Brand, Judith
Van Ijcken, Wilfred
Source
Medline; PMC
abstract
The emergence of viral respiratory pathogens with pandemic potential, such as severe acute respiratory syndrome coronavirus (SARS-CoV) and influenza A H5N1, urges the need for deciphering their pathogenesis to develop new intervention strategies. SARS-CoV infection causes acute lung injury (ALI) that may develop into life-threatening acute respiratory distress syndrome (ARDS) with advanced age correlating positively with adverse disease outcome. The molecular pathways, however, that cause virus-induced ALI/ARDS in aged individuals are ill-defined. Here, we show that SARS-CoV-infected aged macaques develop more severe pathology than young adult animals, even though viral replication levels are similar. Comprehensive genomic analyses indicate that aged macaques have a stronger host response to virus infection than young adult macaques, with an increase in differential expression of genes associated with inflammation, with NF-κB as central player, whereas expression of type I interferon (IFN)-β is reduced. Therapeutic treatment of SARS-CoV-infected aged macaques with type I IFN reduces pathology and diminishes pro-inflammatory gene expression, including interleukin-8 (IL-8) levels, without affecting virus replication in the lungs. Thus, ALI in SARS-CoV-infected aged macaques developed as a result of an exacerbated innate host response. The anti-inflammatory action of type I IFN reveals a potential intervention strategy for virus-induced ALI.
has issue date
2010-02-05
(
xsd:dateTime
)
bibo:doi
10.1371/journal.ppat.1000756
bibo:pmid
20140198
has license
cc-by
sha1sum (hex)
284790100b67133f3228466016a8f98ad096e24d
schema:url
https://doi.org/10.1371/journal.ppat.1000756
resource representing a document's title
Exacerbated Innate Host Response to SARS-CoV in Aged Non-Human Primates
has PubMed Central identifier
PMC2816697
has PubMed identifier
20140198
schema:publication
PLoS Pathog
resource representing a document's body
covid:284790100b67133f3228466016a8f98ad096e24d#body_text
is
schema:about
of
named entity 'differential'
named entity 'virus'
named entity 'macaques'
named entity 'potential'
named entity 'adverse'
named entity 'macaques'
named entity 'ALI'
named entity 'EXACERBATED'
named entity 'INFLAMMATORY'
named entity 'H5N1'
named entity 'EMERGENCE'
named entity 'VIRAL REPLICATION'
named entity 'THE LUNGS'
named entity 'THEIR'
named entity 'INTERLEUKIN-8 '
named entity 'REVEALS'
named entity 'CENTRAL'
named entity 'EXPRESSION'
named entity 'VIRUS'
named entity 'VIRUS INFECTION'
named entity 'HAVE'
named entity 'PANDEMIC'
named entity 'ADVANCED AGE'
named entity 'YOUNG ADULT'
named entity 'POTENTIAL'
named entity 'INCREASE'
named entity 'INTERVENTION'
named entity 'GENES'
named entity 'CAUSE'
named entity 'LIFE'
named entity 'AGED'
named entity 'INFLAMMATION'
named entity 'MACAQUES'
named entity 'ANTI-INFLAMMATORY ACTION'
named entity 'COMPREHENSIVE'
named entity 'WITH TYPE'
named entity 'ACUTE RESPIRATORY DISTRESS SYNDROME'
named entity 'GENOMIC'
named entity 'ASSOCIATED WITH'
named entity 'NF-KB'
named entity 'PATHOGENESIS'
named entity 'TYPE I INTERFERON'
named entity 'THERAPEUTIC'
named entity 'ILL-DEFINED'
named entity 'INDIVIDUALS'
named entity 'INDUCED'
named entity 'AS A RESULT OF'
named entity 'REDUCED'
named entity 'HOST RESPONSE'
named entity 'TYPE I'
named entity 'HOST RESPONSE'
named entity 'ACUTE LUNG INJURY'
named entity 'INTERFERON '
named entity 'SARS-COV'
named entity 'GENE EXPRESSION'
named entity 'INFECTED'
named entity 'INTERVENTION STRATEGIES'
named entity 'STRATEGY'
named entity 'INCLUDING'
named entity 'NON-'
named entity 'AGED'
named entity 'HUMAN'
named entity 'DISEASE OUTCOME'
named entity 'ANIMALS'
named entity 'EXACERBATED'
named entity 'AFFECTING'
named entity 'SARS-COV INFECTION'
named entity 'LEVELS'
named entity 'RESPONSE TO VIRUS'
named entity 'IFN'
named entity 'NEED FOR'
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