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About:
The Tie2-agonist Vasculotide rescues mice from influenza virus infection
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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
The Tie2-agonist Vasculotide rescues mice from influenza virus infection
Creator
Zhang, Haibo
Hwang, David
Leong-Poi, Howard
Kuebler, Wolfgang
Advani, Andrew
Advani, Suzanne
Armstrong, Susan
Dumont, Dan
Lee, Warren
Sugiyama, Michael
Szaszi, Katalin
Tabuchi, Arata
Van Slyke, Paul
Wang, Changsen
Source
PMC
abstract
Seasonal influenza virus infections cause hundreds of thousands of deaths annually while viral mutation raises the threat of a novel pandemic strain. Antiviral drugs exhibit limited efficacy unless administered early and may induce viral resistance. Thus, targeting the host response directly has been proposed as a novel therapeutic strategy with the added potential benefit of not eliciting viral resistance. Severe influenza virus infections are complicated by respiratory failure due to the development of lung microvascular leak and acute lung injury. We hypothesized that enhancing lung endothelial barrier integrity could improve the outcome. Here we demonstrate that the Tie2-agonist tetrameric peptide Vasculotide improves survival in murine models of severe influenza, even if administered as late as 72 hours after infection; the benefit was observed using three strains of the virus and two strains of mice. The effect required Tie2, was independent of viral replication and did not impair lung neutrophil recruitment. Administration of the drug decreased lung edema, arterial hypoxemia and lung endothelial apoptosis; importantly, Vasculotide is inexpensive to produce, is chemically stable and is unrelated to any Tie2 ligands. Thus, Vasculotide may represent a novel and practical therapy for severe infections with influenza.
has issue date
2015-06-05
(
xsd:dateTime
)
bibo:doi
10.1038/srep11030
bibo:pmid
26046800
has license
cc-by
sha1sum (hex)
9a5c1b3f9b311116c99c50ecb181a2e3c71731b4
schema:url
https://doi.org/10.1038/srep11030
resource representing a document's title
The Tie2-agonist Vasculotide rescues mice from influenza virus infection
has PubMed Central identifier
PMC4457136
has PubMed identifier
26046800
schema:publication
Sci Rep
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covid:9a5c1b3f9b311116c99c50ecb181a2e3c71731b4#body_text
is
schema:about
of
named entity 'viral resistance'
named entity 'barrier'
named entity 'lung'
named entity 'influenza'
named entity 'mice'
named entity 'COMPLICATED BY'
named entity 'severe infections'
named entity 'models'
named entity 'microvascular'
named entity 'demonstrate'
named entity 'therapeutic'
named entity 'severe'
named entity 'represent'
named entity 'viral replication'
named entity 'influenza virus'
named entity 'infection'
named entity 'influenza'
named entity 'Tie2'
named entity 'infection'
named entity 'influenza virus'
named entity 'antibody'
named entity 'Amantadine'
named entity 'NaCL'
named entity 'Lysates'
named entity 'assay'
named entity 'H3N2'
named entity 'Switzerland'
named entity 'microscope'
named entity 'density gradient'
named entity 'Supernatant'
named entity 'gavage'
named entity 'murine'
named entity 'peptide'
named entity 'influenza'
named entity 'hypoxemia'
named entity 'infection'
named entity 'monocytic'
named entity 'PBS'
named entity 'polyclonal antibody'
named entity 'VE-cadherin'
named entity 'ng/mL'
named entity 'tissue culture'
named entity 'antiviral drugs'
named entity 'SDS page'
named entity 'Tie2'
named entity 'penicillin'
named entity 'haploinsufficient'
named entity 'apoptotic cells'
named entity 'hypothermia'
named entity 'caspase-3'
named entity 'influenza virus'
named entity 'infection'
named entity 'Flu'
named entity 'streptomycin'
named entity 'hemocytometer'
named entity 'Tie2'
named entity 'mechanism of action'
named entity 'infection'
named entity 'wildtype'
named entity 'sequence homology'
named entity 'ANOVA'
named entity 'infection'
named entity 'Amantadine'
named entity 'influenza virus'
named entity 'ligands'
named entity 'Germany'
named entity 'acute respiratory distress syndrome'
named entity 'global public health'
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