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Mouse model of chronic viral hepatitis

Mouse model of chronic viral hepatitis
慢性病毒性肝炎小鼠模型
批准号:
8101842
负责人:
Ian NICHOLAS Crispe
金额:
$37.59万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-01 至 2012-06-30

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Technical summary: Chronic viral hepatitis is a major cause of morbidity and mortality worldwide, and in this family of diseases the immune system is believed to be responsible for the majority of the tissue damage. Animal models of acute immuno-inflammatory liver damage abound, but there is a need for a model that reproduces the key features of chronic viral hepatitis: liver injury, fibrosis, immune failure, and persistence of the pathogen. We have developed a promising new model, in which persistent infection with an Adeno-Associated Virus vector directs expression of the target antigen to hepatocytes for at least 8 months, while exogenous T cells cause tissue damage and activate stellate cells. Prolonged co-existence of the antigen and the T cells leads to T cell dysfunction. Although this model is based on a replication- defective vector, it is an excellent vehicle to study the interactions of T cells with antigen expressed exclusively in hepatocytes. Unlike murine hepatotropic viruses, the vector model in unlikely to entail adaptations to disable liver immunity; thus we can study the immune response to hepatocellular antigens in isolation. Using this model, in Aim 1 we will test the mechanism of hepatocellular injury during acute and chronic immune inflammation. In Aim 2, we will test the mechanisms of stellate cell activation. In Aim 3 we will test the hypothesis that vector persistence is due to the lack of CD4+ T cell activation, because of a lack of cross-priming. In Specific Aim 4, we will induce chronic relapsing hepatitis, and test whether repeated cycles of inflammation lead to sustained stellate cell activation with liver fibrosis. A model that reproduces chronic liver damage, stellate cell activation and immune dysfunction will be most valuable in generating paradigms useful for mechanistic investigations of the mechanism of action of existing anti-viral therapy, and for the rational design of new therapies. Relevance to public health: The immune system is important in fighting against hepatitis viruses, but in the process immune cells cause damage to the liver. We have developed an entirely new mouse model that will make it possible to distinguish the pathways of immune damage from those that fight invaders. This will open the way to new kinds of treatment for hepatitis.
期刊论文(4)
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科研奖励(0)
会议论文
DOI: 10.1002/hep.23745
发表时间: 2010-09
期刊: HEPATOLOGY
影响因子: 13.5
作者: [Wuensch, Sherry A., Spahn, Jessica, Crispe, Ian N.]
通讯作者: Crispe, Ian N.
Ineffective CD8(+) T-cell immunity to adeno-associated virus can result in prolonged liver injury and fibrogenesis.
CD8(+) T 细胞对腺相关病毒的无效免疫可导致长期肝损伤和纤维化。
DOI: 10.1016/j.ajpath.2011.08.004
发表时间: 2011
期刊: The American journal of pathology
影响因子: --
作者: [Spahn,Jessica, Pierce,RobertH, Crispe,IanN]
通讯作者: Crispe,IanN
DOI: 10.1002/hep.22869
发表时间: 2009-06
期刊: HEPATOLOGY
影响因子: 13.5
作者: [Giannandrea, Matthew, Pierce, Robert H., Crispe, Ian Nicholas]
通讯作者: Crispe, Ian Nicholas
DOI: 10.1002/hep.24508
发表时间: 2011-10
期刊: HEPATOLOGY
影响因子: 13.5
作者: [Ebrahimkhani, Mohammad R., Mohar, Isaac, Crispe, Ian N.]
通讯作者: Crispe, Ian N.
Adaptive Liver Tolerance via LSECs
  • 批准号:
    10221498
  • 项目类别:
  • 资助金额:
    $38.88万
  • 财政年份:
    2018
  • 负责人:
    Ian NICHOLAS Crispe
  • 依托单位:
Adaptive Liver Tolerance via LSECs
  • 批准号:
    9788247
  • 项目类别:
  • 资助金额:
    $38.88万
  • 财政年份:
    2018
  • 负责人:
    Ian NICHOLAS Crispe
  • 依托单位:
Adaptive Liver Tolerance via LSECs
  • 批准号:
    10457946
  • 项目类别:
  • 资助金额:
    $38.88万
  • 财政年份:
    2018
  • 负责人:
    Ian NICHOLAS Crispe
  • 依托单位:
Help and suppression in liver tolerance
  • 批准号:
    9442460
  • 项目类别:
  • 资助金额:
    $30.17万
  • 财政年份:
    2017
  • 负责人:
    Ian NICHOLAS Crispe
  • 依托单位:
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