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About:
CD4–CD8-T cells contribute to the persistence of viral hepatitis by striking a delicate balance in immune modulation
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schema:ScholarlyArticle
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wasabi.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
CD4–CD8-T cells contribute to the persistence of viral hepatitis by striking a delicate balance in immune modulation
Creator
Guo, Wei
Sun, Ying
Luo, Xiaoping
Ning, Qin
Wang, Hongwu
Xi, Dong
Yan, Weiming
Chen, Tao
Han, Meifang
Lu, Yulei
Qin, Xiaomin
Wang, Xiaojing
Wu, Di
Zhang, Jiangguo
Source
Elsevier; Medline; PMC
abstract
Abstract Viral hepatitis remains the most common cause of liver disease and a major public health problem. Here, we focus on the role of CD4 CD8 double negative T (DN T) cells involved in the mechanisms of viral persistence in hepatitis. C3H/HeJ mice infected with murine hepatitis virus strain 3 (MHV-3) were used to display chronic viral hepatitis. DN T cells dramatically increased in MHV-3 infected mice. Adoptive transfer of DN T cells from MHV-3 infected mice led to a significant increase in mice survival. The DN T cells with production of IFN-γ and IL-2 are able to kill virus-specific CD8+ T cells via the Fas/FasL dependent pathway. The delicate balance of multiple effects of DN T cells may lead to viral persistence in MHV-3 induced hepatitis. In short, our study identified DN T cells contributing to viral persistence in MHV-3 induced hepatitis in C3H/HeJ mice, which provides a rationale for modulating DN T cells for the management of viral hepatitis.
has issue date
2012-11-30
(
xsd:dateTime
)
bibo:doi
10.1016/j.cellimm.2012.11.010
bibo:pmid
23261832
has license
els-covid
sha1sum (hex)
5b11bcba84104ee1180caaa51adc51bcefbc7dfb
schema:url
https://doi.org/10.1016/j.cellimm.2012.11.010
resource representing a document's title
CD4–CD8-T cells contribute to the persistence of viral hepatitis by striking a delicate balance in immune modulation
has PubMed Central identifier
PMC7094652
has PubMed identifier
23261832
schema:publication
Cellular Immunology
resource representing a document's body
covid:5b11bcba84104ee1180caaa51adc51bcefbc7dfb#body_text
is
schema:about
of
named entity 'STRIKING'
named entity 'MHV'
named entity 'CD4'
named entity 'INCREASED'
named entity 'ADOPTIVE TRANSFER'
named entity 'PROVIDES'
named entity 'SIGNIFICANT'
named entity 'INVOLVED'
named entity 'VIRUS'
named entity 'LED'
named entity 'OF LIVER DISEASE'
named entity 'OUR'
named entity 'TO DISPLAY'
named entity 'VIRAL HEPATITIS'
named entity 'SURVIVAL'
named entity 'INFECTED'
named entity 'CD4 CD8'
named entity 'NEGATIVE'
named entity 'HERE'
named entity 'IFN'
named entity 'PUBLIC HEALTH'
named entity 'COMMON'
named entity 'FOCUS'
named entity 'BALANCE'
named entity 'VIRAL HEPATITIS'
named entity 'INCREASE'
named entity 'EFFECTS'
named entity 'KILL'
named entity 'T CELLS'
named entity 'PATHWAY'
named entity 'HEALTH PROBLEM'
named entity 'A MAJOR'
named entity 'PRODUCTION'
named entity 'PERSISTENCE'
named entity 'CD8'
named entity 'T CELLS'
named entity 'IMMUNE MODULATION'
named entity 'CONTRIBUTE '
named entity 'CONTRIBUTING'
named entity 'DOUBLE'
named entity 'MURINE HEPATITIS VIRUS STRAIN 3'
named entity 'STUDY'
named entity 'CD8'
named entity 'INDUCED'
named entity 'ROLE'
named entity 'CELLS'
named entity 'BALANCE'
named entity 'C3H'
named entity 'IDENTIFIED'
named entity 'USED'
named entity 'MODULATING'
named entity 'FAS'
named entity 'CAUSE'
named entity 'SHORT'
named entity 'MULTIPLE'
named entity 'VIRAL PERSISTENCE'
named entity 'IL-2'
named entity 'MHV'
named entity 'MECHANISMS'
named entity 'DEPENDENT'
named entity 'SPECIFIC'
named entity 'HEPATITIS'
named entity 'CHRONIC VIRAL HEPATITIS'
named entity 'MICE'
named entity 'RATIONALE'
named entity 'LEAD'
named entity 'MANAGEMENT'
covid:arg/5b11bcba84104ee1180caaa51adc51bcefbc7dfb
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