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About:
The contact activation system as a potential therapeutic target in patients with 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
title
The contact activation system as a potential therapeutic target in patients with COVID‐19
Creator
Mccarty, J
Faha,
Jeffrey, |
Shatzel, Joseph
Aslan, Joseph
Gailani, David
Gruber, Andras
Lorentz, Christina
Deloughery Bs, Emma
Hinds Phd, Monica
Owen, |
Tucker Phd, Erik
Weitz, I
source
Medline; PMC; WHO
abstract
Coronavirus disease 2019 (COVID‐19) is predicted to overwhelm health care capacity in the United States and worldwide, and, as such, interventions that could prevent clinical decompensation and respiratory compromise in infected patients are desperately needed. Excessive cytokine release and activation of coagulation appear to be key drivers of COVID‐19 pneumonia and associated mortality. Contact activation has been linked to pathologic upregulation of both inflammatory mediators and coagulation, and accumulating preclinical and clinical data suggest it to be a rational therapeutic target in patients with COVID‐19. Pharmacologic inhibition of the interaction between coagulation factors XI and XII has been shown to prevent consumptive coagulopathy, pathologic systemic inflammatory response, and mortality in at least 2 types of experimental sepsis. Importantly, inhibition of contact activation also prevented death from Staphylococcus aureus–induced lethal systemic inflammatory response syndrome in nonhuman primates. The contact system is likely dispensable for hemostasis and may not be needed for host immunity, suggesting it to be a reasonably safe target that will not result in immunosuppression or bleeding. As a few drugs targeting contact activation are already in clinical development, immediate clinical trials for their use in patients with COVID‐19 are potentially feasible for the prevention or treatment of respiratory distress.
has issue date
2020-05-15
(
xsd:dateTime
)
bibo:doi
10.1002/rth2.12349
bibo:pmid
32542210
has license
cc-by-nc-nd
sha1sum (hex)
4ecf7625524660e5e0ffd39502be6dc753542fff
schema:url
https://doi.org/10.1002/rth2.12349
resource representing a document's title
The contact activation system as a potential therapeutic target in patients with COVID‐19
has PubMed Central identifier
PMC7264624
has PubMed identifier
32542210
schema:publication
Res Pract Thromb Haemost
resource representing a document's body
covid:4ecf7625524660e5e0ffd39502be6dc753542fff#body_text
is
schema:about
of
named entity 'cytokine'
named entity 'sepsis'
named entity 'release'
named entity 'types'
named entity 'activation'
named entity 'prevention'
named entity 'inflammatory response'
named entity 'Contact'
named entity 'mortality'
named entity 'The contact'
named entity 'consumptive coagulopathy'
named entity 'worldwide'
named entity 'decompensation'
named entity 'drugs'
named entity 'clinical trials'
named entity 'prevent'
named entity 'patients'
named entity 'target'
named entity 'respiratory distress'
named entity 'Pharmacologic'
named entity 'hemostasis'
named entity 'inflammatory mediators'
named entity 'consumptive coagulopathy'
named entity 'host immunity'
named entity 'pneumonia'
named entity 'COVID-19'
named entity 'coagulation factors'
named entity 'decompensation'
named entity 'coagulopathy'
named entity 'FXI'
named entity 'hemostasis'
named entity 'FXI'
named entity 'animal models'
named entity 'mice'
named entity 'FXI'
named entity 'hereditary angioedema'
named entity 'FXI'
named entity 'Holstein cattle'
named entity 'inflammatory cytokine'
named entity 'deficient mice'
named entity 'Pathologic'
named entity 'coagulopathy'
named entity 'FXI'
named entity 'hepatic'
named entity 'thromboprophylaxis'
named entity 'factor XII'
named entity 'recombinant'
named entity 'antibody-mediated'
named entity 'hepatic'
named entity 'heparin'
named entity 'pneumonia'
named entity 'mouse model'
named entity 'viral infections'
named entity 'lungs'
named entity 'KKS'
named entity 'FXI'
named entity 'peritoneal'
named entity 'inflammation'
named entity 'IL-6'
named entity 'plasma'
named entity 'host defense'
named entity 'factor XI'
named entity 'coagulation'
named entity 'wild-type'
named entity 'plasma'
named entity 'inflammatory markers'
named entity 'IL-6'
named entity 'coagulation'
named entity 'murine'
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