Role of HCV* Hepatocyte in Regulation of Antiviral T cell Immunity
Role of HCV* Hepatocyte in Regulation of Antiviral T cell Immunity
批准号:
8380559
负责人:
Young S. Hahn
金额:
$23.14万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
未结题
起止时间:
2005-09-15 至
关键词:
AcuteAntiviral AgentsApoptosisBerylliumCD4 Positive T LymphocytesCD8B1 geneCTLA4 geneCell physiologyCellsChronicCoculture TechniquesColoradoDevelopmentDiscontinuous CapillaryEpigenetic ProcessFunctional disorderGenesGenomeHepatitis CHepatitis C virusHepatocyteHumanImmuneImmunityImpairmentInfectionInterferon Type IIInterferonsInterleukin-17Interleukin-2LigandsLiverLiver CirrhosisMediatingOutcomePatientsPlayPopulationPrimary carcinoma of the liver cellsProductionProteinsRegulationResearchRoleShapesSiteStagingT cell differentiationT cell responseT-LymphocyteT-Lymphocyte SubsetsTLR3 geneTestingTherapeuticViraladaptive immunitybasecytokinedesigninsightinterleukin-22transcription factor
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The project 2 of HCV Cooperative Research Center alms to understand the regulation of adaptive Immunity
via the Interaction of HCV-infected hepatocytes with CD4 T cells during acute HCV Infection. HCV Infection
In humans is remarkably efficient In establishing viral persistence, leading to the development of liver
cirrhosis and hepatocellular carcinoma. CDS T cells are Involved in controlling HCV Infection; but. In chronic
HCV patients, severe CD4 and CDS T cell dysfunction has been observed. This suggests that HCV may
employ some mechanism to counteract or possibly suppress the host T cell response. The primary site of
viral replication is within hepatocytes in the liver. During HCV Infection, there is the increased population of
CD4 T cells in the liver sinusoid, which allows close contact with HCV-infected hepatocytes. To determine
whether the Interaction of HCV-infected hepatocytyes with CD4 T cells alters CD4 T cell helper function on
shaping CDS T cell effector antiviral activity, we conducted co-culture studies of HCV-infected hepatocytes
with CD4 T cells. Our preliminary studies, we demonstrated that hepatocytes expressing whole HCV
proteins (I.e. HCV+ hepatocytes) upregulated the ligand of PD-1 negative costimulatory molecule, B7-H1,
and TGF-b synthesis. In addition, HCV+ hepatocytes are capable of impairing CD4 T cell function including
Inhibition of IFN-g production. Based on these findings, we hypothesize that HCV+ hepatocyte-mediated
Inhibition of CD4 T cell function plays a pivotal role In Impairing antiviral CDS T cell effector function. To test
this hypothesis, we propose three specific alms, we will first explore the mechanism for HCV+ hepatocytemediated
Inhibition of CD4 T cell responses. Second, we will determine the impact of HCV+ hepatocyteinduced
CD4 T cell dysfunction on regulating antiviral CDS T cell effector function. Lastly, we will examine
the status of CD4 T cell differentiation and correlate it with the outcome of HCV infection during acute HCV
patients. Results of these studies will provide valuable insight Into designing therapeutic strategies against
to HCV Infection.
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Role of HCV exosomes in intercellular communication
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批准号:10549367
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项目类别:
-
资助金额:$42.41万
-
财政年份:2020
-
负责人:Young S. Hahn
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依托单位:
Role of HCV exosomes in intercellular communication
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批准号:10833764
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项目类别:
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资助金额:$5.77万
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财政年份:2020
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负责人:Young S. Hahn
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依托单位:
Role of HCV exosomes in intercellular communication
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批准号:10360522
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项目类别:
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资助金额:$48.85万
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财政年份:2020
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负责人:Young S. Hahn
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依托单位:
Control of Influenza Infection by Lipid Mediators and Macrophages
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批准号:10317033
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项目类别:
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资助金额:$54.98万
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财政年份:2018
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负责人:Young S. Hahn
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依托单位:
Role of HCV in aberrant APC activation/function
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批准号:8678833
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项目类别:
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资助金额:$39.21万
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财政年份:2012
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负责人:Young S. Hahn
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依托单位:
Role of HCV in aberrant APC activation/function
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批准号:8468021
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项目类别:
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资助金额:$36.86万
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财政年份:2012
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负责人:Young S. Hahn
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依托单位:
Role of HCV in aberrant APC activation/function
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批准号:8860103
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项目类别:
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资助金额:$39.21万
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财政年份:2012
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负责人:Young S. Hahn
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依托单位:
Role of HCV in aberrant APC activation/function
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批准号:8371025
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项目类别:
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资助金额:$39.21万
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财政年份:2012
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负责人:Young S. Hahn
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依托单位:
Role of HCV in aberrant APC activation/function
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批准号:9095220
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项目类别:
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资助金额:$39.21万
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财政年份:2012
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负责人:Young S. Hahn
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依托单位:
Regulation of CD8+ T cell responses via liver NK-DC crosstalk
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批准号:7746094
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项目类别:
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资助金额:$25.51万
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财政年份:2009
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负责人:Young S. Hahn
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依托单位:
Role of HCV* Hepatocyte in Regulation of Antiviral T cell Immunity
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批准号:7919878
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项目类别:
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资助金额:$23.23万
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财政年份:2005
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负责人:Young S. Hahn
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依托单位:
Suppression of HCV-specific CD4+ T Cells by Core Protein
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批准号:7014423
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项目类别:
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资助金额:$21.05万
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财政年份:2005
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负责人:Young S. Hahn
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依托单位:
Role of HCV* Hepatocyte in Regulation of Antiviral T cell Immunity
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批准号:8712326
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项目类别:
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资助金额:$22.8万
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财政年份:2005
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负责人:Young S. Hahn
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依托单位:
Role of HCV* Hepatocyte in Regulation of Antiviral T cell Immunity
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批准号:8519232
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项目类别:
-
资助金额:$19.96万
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财政年份:2005
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负责人:Young S. Hahn
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依托单位:
Role of HCV* Hepatocyte in Regulation of Antiviral T cell Immunity
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批准号:8317649
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项目类别:
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资助金额:$22.2万
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财政年份:2005
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负责人:Young S. Hahn
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依托单位:
Alteration of innate immunity by HCV core
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批准号:7324055
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项目类别:
-
资助金额:$28.24万
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财政年份:2004
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负责人:Young S. Hahn
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依托单位:
Alteration of innate immunity by HCV core
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批准号:6986137
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项目类别:
-
资助金额:$29.65万
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财政年份:2004
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负责人:Young S. Hahn
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依托单位:
Alteration of innate immunity by HCV core
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批准号:7534064
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项目类别:
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资助金额:$28.23万
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财政年份:2004
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负责人:Young S. Hahn
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依托单位:
Impaired T cell function by HCV core
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批准号:6740680
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项目类别:
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资助金额:$30.3万
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财政年份:2004
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负责人:Young S. Hahn
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依托单位:
Impaired T cell function by HCV core
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批准号:7228960
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项目类别:
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资助金额:$28.81万
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财政年份:2004
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负责人:Young S. Hahn
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依托单位:
海外基金