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About:
Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
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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
Values
type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
Creator
Fouchier, Ron
Rimmelzwaan, Guus
Sutter, Gerd
Volz, Asisa
Altenburg, Arwen
De Swart, Rik
Macloughlin, Ronan
Van Amerongen, Geert
De Vries, Rory
Hendriks, Rudi
Li, Bobby
Van De Sandt, Carolien
topic
covid:9eb3ea6224aabe868a10af37dc829b9636be5856#this
Source
PMC
abstract
Modified Vaccinia virus Ankara (MVA) is a promising vaccine vector with an excellent safety profile. However, despite extensive pre-clinical and clinical testing, surprisingly little is known about the cellular tropism of MVA, especially in relevant animal species. Here, we performed in vitro, ex vivo and in vivo experiments with recombinant MVA expressing green fluorescent protein (rMVA-GFP). In both human peripheral blood mononuclear cells and mouse lung explants, rMVA-GFP predominantly infected antigen presenting cells. Subsequent in vivo experiments performed in mice, ferrets and non-human primates indicated that preferential targeting of dendritic cells and alveolar macrophages was observed after respiratory administration, although subtle differences were observed between the respective animal species. Following intramuscular injection, rMVA-GFP was detected in interdigitating cells between myocytes, but also in myocytes themselves. These data are important in advancing our understanding of the basis for the immunogenicity of MVA-based vaccines and aid rational vaccine design and delivery strategies.
has issue date
2017-08-17
(
xsd:dateTime
)
bibo:doi
10.1038/s41598-017-08719-y
bibo:pmid
28819261
has license
cc-by
sha1sum (hex)
9eb3ea6224aabe868a10af37dc829b9636be5856
schema:url
https://doi.org/10.1038/s41598-017-08719-y
resource representing a document's title
Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
has PubMed Central identifier
PMC5561217
has PubMed identifier
28819261
schema:publication
Sci Rep
resource representing a document's body
covid:9eb3ea6224aabe868a10af37dc829b9636be5856#body_text
is
http://vocab.deri.ie/void#inDataset
of
proxy:http/ns.inria.fr/covid19/9eb3ea6224aabe868a10af37dc829b9636be5856
is
schema:about
of
named entity 'OUR'
named entity 'MYOCYTES'
named entity 'DELIVERY'
named entity 'INTRAMUSCULAR INJECTION'
named entity 'INTERDIGITATING CELLS'
named entity 'VACCINES'
named entity 'BUT'
named entity 'IMPORTANT'
named entity 'STRATEGIES'
named entity 'respective'
covid:arg/9eb3ea6224aabe868a10af37dc829b9636be5856
named entity 'ADMINISTRATION'
named entity 'AID'
named entity 'DATA'
named entity 'BASED'
named entity 'MVA'
named entity 'BASIS'
named entity 'THESE'
named entity 'GFP'
named entity 'ADVANCING'
named entity 'OBSERVED'
named entity 'FOLLOWING'
named entity 'IMMUNOGENICITY'
named entity 'RESPIRATORY'
named entity 'DETECTED'
named entity 'ANIMAL SPECIES'
named entity 'UNDERSTANDING'
named entity 'aid'
named entity 'intramuscular injection'
named entity 'myocytes'
named entity 'intramuscular injection'
named entity 'Mustela'
named entity 'GFP'
named entity 'medetomidine'
named entity 'Blood samples'
named entity 'APC'
named entity 'Roche diagnostics'
named entity 'non-human primates'
named entity 'HLA'
named entity 'phenotypically'
named entity 'IM injection'
named entity 'alveolar macrophages'
named entity 'CLSM'
named entity 'FACS'
named entity 'biotin'
named entity 'AER'
named entity 'amphotericin'
named entity 'Lonza'
named entity 'NALT'
named entity 'CD11c'
named entity 'lysis buffer'
named entity 'CD19'
named entity 'inhalation'
named entity 'GFP'
named entity 'phenotype'
named entity 'GFP'
named entity 'infection'
named entity 'inoculation'
named entity 'present antigens'
named entity 'non-human primates'
named entity 'GFP'
named entity 'PCR'
named entity 'Vaccination'
named entity 'inoculation'
named entity 'neutrophils'
named entity 'HPA'
named entity 'CD11c'
named entity 'refractory'
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