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About:
Evaluation of Zika Virus-specific T-cell Responses in Immunoprivileged Organs of Infected Ifnar1(-/-) Mice
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
document(s)
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
Evaluation of Zika Virus-specific T-cell Responses in Immunoprivileged Organs of Infected Ifnar1(-/-) Mice
Creator
Li, Xiangdong
Zhao, Min
Zhao, Yingze
Gao, George
Liu, Kefang
Zhang, X
Lu, Xuancheng
Zhang, Hangjie
Zhang, Yongli
Ma, Wenqiang
Zhang, Fuping
Gao, X
Li, F
Liu, G
Liu, W
Liu, William
Lu, Y
Ma, H
Zhang, Citation
Zhang, Y
Zhao, K
Zhao, M
topic
covid:4090c4a0e8cead64dd9e44a1610fb4f557fefdcf#this
Source
Medline; PMC
abstract
The Zika virus (ZIKV) can induce inflammation in immunoprivileged organs (e.g., the brain and testis), leading to the Guillain-Barré syndrome and damaging the testes. During an infection with the ZIKV, immune cells have been shown to infiltrate into the tissues. However, the cellular mechanisms that define the protection and/or immunopathogenesis of these immune cells during a ZIKV infection are still largely unknown. Herein, we describe methods to evaluate the virus-specific T-cell functionality in these immunoprivileged organs of ZIKV-infected mice. These methods include a) a ZIKV infection and vaccine inoculation in Ifnar1(-/-) mice; b) histopathology, immunofluorescence, and immunohistochemistry assays to detect the virus infection and inflammation in the brain, testes, and spleen; c) the preparation of a tetramer of ZIKV-derived T-cell epitopes; d) the detection of ZIKV-specific T cells in the monocytes isolated from the brain, testes, and spleen. Using these approaches, it is possible to detect the antigen-specific T cells that have infiltrated into the immunoprivileged organs and to evaluate the functions of these T cells during the infection: potential immune protection via virus clearance and/or immunopathogenesis to exacerbate the inflammation. These findings may also help to clarify the contribution of T cells induced by the immunization against ZIKV.
has issue date
2018-10-17
(
xsd:dateTime
)
bibo:doi
10.3791/58110
bibo:pmid
30394402
has license
cc-by-nc-nd
sha1sum (hex)
4090c4a0e8cead64dd9e44a1610fb4f557fefdcf
schema:url
https://doi.org/10.3791/58110
resource representing a document's title
Evaluation of Zika Virus-specific T-cell Responses in Immunoprivileged Organs of Infected Ifnar1(-/-) Mice
has PubMed Central identifier
PMC6235543
has PubMed identifier
30394402
schema:publication
J Vis Exp
resource representing a document's body
covid:4090c4a0e8cead64dd9e44a1610fb4f557fefdcf#body_text
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http://vocab.deri.ie/void#inDataset
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proxy:http/ns.inria.fr/covid19/4090c4a0e8cead64dd9e44a1610fb4f557fefdcf
is
schema:about
of
named entity 'organs'
named entity 'assays'
named entity 'testes'
named entity 'virus-specific'
named entity 'isolated'
named entity 'Zika virus'
named entity 'induced'
named entity 'infection'
named entity 'T cells'
named entity 'testis'
named entity 'T cells'
named entity 'immunohistochemistry'
named entity 'testes'
named entity 'inflammation'
named entity 'functions'
named entity 'spleen'
named entity 'immunization'
named entity 'antigen'
named entity 'virus'
named entity 'immunoprivileged organs'
named entity 'ZIKV'
named entity 'immunofluorescence'
named entity 'infection'
named entity 'immunization'
named entity 'virus'
named entity 'immunopathogenesis'
named entity 'spleen'
named entity 'ZIKV'
named entity 'immune cells'
named entity 'ZIKV'
named entity 'immunoprivileged organs'
named entity 'testis'
named entity 'functionality'
named entity 'mice'
named entity 'ZIKV'
named entity 'mice'
named entity 'fat'
named entity 'viral vaccine'
named entity 'T-cell'
named entity 'refolding'
named entity 'infection'
named entity 'cellular immune responses'
named entity 'infection'
named entity 'mice'
named entity 'immunopathogenesis'
named entity 'immunoprivileged organs'
named entity 'immunofluorescence assay'
named entity 'immunoprivileged organs'
named entity 'epitope'
named entity 'flow cytometry'
named entity 'ZIKV'
named entity 'CD8 +'
named entity 'murine'
named entity 'intravenous'
named entity 'CNS'
named entity 'correlation'
named entity 'murine models'
named entity 'CD8 +'
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