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About:
Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
wasabi.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
Attributes
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19
Creator
Schwartz, Robert
Oishi, Kohei
Liu, Wen-Chun
Albrecht, Randy
Jordan, Tristan
Lim, Jean
Tenoever, Benjamin
Blanco-Melo, Daniel
Hoagland, Daisy
Møller, Rasmus
Nilsson-Payant, Benjamin
Panis, Maryline
Sachs, David
Uhl, Skyler
Wang, Taia
Source
Elsevier; Medline; PMC
abstract
Viral pandemics, such as the one caused by SARS-CoV-2, pose an imminent threat to humanity. Because of its recent emergence, there is a paucity of information regarding viral behavior and host response following SARS-CoV-2 infection. Here we offer an in-depth analysis of the transcriptional response to SARS-CoV-2 compared with other respiratory viruses. Cell and animal models of SARS-CoV-2 infection, in addition to transcriptional and serum profiling of COVID-19 patients, consistently revealed a unique and inappropriate inflammatory response. This response is defined by low levels of type I and III interferons juxtaposed to elevated chemokines and high expression of IL-6. We propose that reduced innate antiviral defenses coupled with exuberant inflammatory cytokine production are the defining and driving features of COVID-19.
has issue date
2020-05-15
(
xsd:dateTime
)
bibo:doi
10.1016/j.cell.2020.04.026
bibo:pmid
32416070
has license
no-cc
sha1sum (hex)
dea4b05ab91f7eb501a9205c53c2f510bdccf147
schema:url
https://doi.org/10.1016/j.cell.2020.04.026
resource representing a document's title
Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19
has PubMed Central identifier
PMC7227586
has PubMed identifier
32416070
schema:publication
Cell
resource representing a document's body
covid:dea4b05ab91f7eb501a9205c53c2f510bdccf147#body_text
is
schema:about
of
named entity 'viral'
named entity 'addition'
named entity 'infection'
named entity 'SARS-CoV-2'
named entity 'vivo'
named entity 'induces'
named entity 'PRO-'
named entity 'IN VIVO'
named entity 'IMMINENT'
named entity 'SERUM'
named entity 'RESPIRATORY VIRUSES'
named entity 'Viral'
named entity 'This'
named entity 'defining'
named entity 'IAV'
named entity 'viruses'
named entity 'pattern recognition receptors'
named entity 'SARS-CoV-2'
named entity 'IFN'
named entity 'respiratory tract'
named entity 'biopsies'
named entity 'MERS'
named entity 'physiological'
named entity 'IL-6'
named entity 'CXCL9'
named entity 'chemokines'
named entity 'CXCL9'
named entity 'type I'
named entity 'host response'
named entity 'juxtaposed'
named entity 'emergence'
named entity 'interferons'
named entity 'SARS-CoV-2'
named entity 'infection'
named entity 'pro-inflammatory'
named entity 'infection'
named entity 'transcriptional'
named entity 'chemokine'
named entity 'SARS-CoV-2'
named entity 'infection'
named entity 'Krammer'
named entity 'ACE2'
named entity 'IRF9'
named entity 'virus infection'
named entity 'RNA-seq'
named entity 'IFNA10'
named entity 'ABCE1'
named entity 'inflammatory response'
named entity 'plaque assays'
named entity 'epithelial'
named entity 'virus replication'
named entity 'SARS-CoV-2'
named entity 'cell culture'
named entity 'fever'
named entity 'chemokine'
named entity 'Western blot'
named entity 'IFN'
named entity 'SARS-CoV-2'
named entity 'LPAR6'
named entity 'Calu-3'
named entity 'dramatic increase'
named entity 'bronchial'
named entity 'DHX58'
named entity 'ISGs'
named entity 'chemokines'
named entity 'CXCL8'
named entity 'orders of magnitude'
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