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About:
Cloning, expression and characterization of ferret CXCL10
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schema:ScholarlyArticle
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covidontheweb.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
Cloning, expression and characterization of ferret CXCL10
Creator
Banner, David
Danesh, Ali
Xu, Luoling
Ran, Longsi
Rowe, Thomas
Cameron, Cheryl
Kelvin, David
Czub, Marcus
Seneviratne, Charit
Cameron, Mark
Jonsson, Colleen
Bosinger, Steven
Devries, Mark
Kelvin, Alyson
Source
Elsevier; Medline; PMC
abstract
Chemokines and their receptors function in the recruitment and activation of cells of the immune system to sites of inflammation. As such, chemokines play an important role in mediating pathophysiological events during microbial infection. In particular, CXCL9, 10 and 11 and their cognate receptor CXCR3 have been associated with the clinical course of several infectious diseases, including severe acute respiratory syndrome (SARS) and influenza. While CXCL9, 10 and 11 share the same receptor and have overlapping functions, each can also have unique activity in host defense. The lack of a preferred characterized animal model for SARS has brought our attention to ferrets, which have been used for years in influenza studies. The lack of immunological reagents for ferrets prompted us to clone CXCL9, 10, 11 and CXCR3 and, in the case of CXCL10, to express the gene as a recombinant protein. In this study we demonstrate that endogenous ferret CXCL10 exhibits similar mRNA expression patterns in the lungs of deceased SARS patients and ferrets experimentally infected with SARS coronavirus. This study therefore represents an important step towards development of the ferret as a model for the role of CXCL9, 10 and 11:CXCR3 axis in severe viral infections.
has issue date
2008-03-01
(
xsd:dateTime
)
bibo:doi
10.1016/j.molimm.2007.09.018
bibo:pmid
18006061
has license
green-oa
sha1sum (hex)
20a38a054a302914d42eb2b228afb705702de803
schema:url
https://doi.org/10.1016/j.molimm.2007.09.018
resource representing a document's title
Cloning, expression and characterization of ferret CXCL10
has PubMed Central identifier
PMC5653245
has PubMed identifier
18006061
schema:publication
Molecular Immunology
resource representing a document's body
covid:20a38a054a302914d42eb2b228afb705702de803#body_text
is
schema:about
of
named entity 'preferred'
named entity 'immune system'
named entity 'REAGENTS'
named entity 'ASSOCIATED WITH'
named entity 'MRNA EXPRESSION'
named entity 'INCLUDING'
named entity 'LACK'
named entity 'STUDIES'
named entity 'CLONE'
named entity 'STUDY'
named entity 'MICROBIAL INFECTION'
named entity 'INFLAMMATION'
named entity 'MODEL'
named entity 'PATTERNS'
named entity 'INFECTIOUS DISEASES'
named entity 'FERRET'
named entity 'ACTIVITY'
named entity 'RECEPTOR'
named entity 'CHEMOKINES'
named entity 'ACTIVATION'
named entity 'DECEASED'
named entity 'SEVERE ACUTE RESPIRATORY SYNDROME'
named entity 'USED'
named entity 'RECRUITMENT'
named entity 'CXCR3'
named entity 'THEIR'
named entity 'OVERLAPPING'
named entity 'TO EXPRESS'
named entity 'CHARACTERIZATION'
named entity 'CXCL10'
named entity 'CLONING'
named entity 'FERRET'
named entity 'EXPRESSION'
named entity 'ATTENTION'
named entity 'CXCL10'
named entity 'SEVERE VIRAL INFECTIONS'
named entity 'ANIMAL MODEL'
named entity 'FUNCTION'
named entity 'MEDIATING'
named entity 'IMMUNE SYSTEM'
named entity 'SHARE'
named entity 'INFLUENZA'
named entity 'PARTICULAR'
named entity 'GENE'
named entity 'RECEPTORS'
named entity 'HAVE'
named entity 'CASE'
named entity 'FERRETS'
named entity 'HOST DEFENSE'
named entity 'EXHIBITS'
named entity 'OUR'
named entity 'SITES'
named entity 'ROLE'
named entity 'PREFERRED'
named entity 'IMPORTANT'
named entity 'RECOMBINANT PROTEIN'
named entity 'ENDOGENOUS'
named entity 'BROUGHT'
named entity 'SARS CORONAVIRUS'
named entity 'SARS'
named entity 'FUNCTIONS'
named entity 'THE LUNGS'
named entity 'INFECTED'
named entity 'YEARS'
named entity 'PATIENTS'
named entity 'PLAY'
named entity 'PROMPTED'
named entity 'CELLS'
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