Astrocytes-Innate & Adaptive Immune Response to Virus
Astrocytes-Innate & Adaptive Immune Response to Virus
批准号:
6893347
负责人:
Pamela Ann Carpentier
金额:
$2.31万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-09-01 至 2006-07-31
关键词:
antibody inhibitorantigen presentationantigen presenting cellantiviral antibodyastrocytescell linechemokineflow cytometrygenetically modified animalsglial fibrillary acidic proteingreen fluorescent proteinshost organism interactionimmune responseimmunityinfectious encephalomyelitisinterleukin 1kinase inhibitorlaboratory mousemicrogliamultiple sclerosismurine encephalomyelitis virusmyelinneuroimmunomodulationneuropathologypolymerase chain reactionpredoctoral investigatorprotein structure functionreceptor expressiontissue /cell culturetoll like receptor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Theiler's murine encephalomyelitis virus (TMEV) establishes a persistent central nervous system (CNS) infection, leading to the development of an autoimmune demyelinating disease. Because of its autoimmune nature and the prominent infiltration of CD4+ T cells and phagocytes, TMEV-induced demyelinating disease (TMEV-IDD) is considered a highly relevant animal model for multiple sclerosis. The innate immune response is the host first line of defense and leads to activation of antigen presenting cell (APC) functions and production of immune effector molecules. In the CNS glial cells (microglia and astrocytes) can respond vigorously to infection and are the major cells in which TMEV persists. Activation of innate immune responses in these cells may contribute directly to demyelination or to epitope spreading of the immune response to myelin antigens. Preliminary data shows that astrocytes express Toll like receptors (TLRs) important in activating innate anti-viral responses and that ligation of these receptors can result in the upregulation of inflammatory cytokines and APC functions of astrocytes. This proposal will thus test the overall hypothesis that astrocytes can respond to TMEV infection through the activation of TLRs by upregulating innate immune, APC and effector functions, and that this activation plays a significant role in the chronic pathogenesis of TMEV-IDD.
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会议论文
Maternal Inflammation Alters Fetal Brain Development via Tumor necrosis Factor-al
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批准号:7614662
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项目类别:
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资助金额:$4.96万
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财政年份:2008
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负责人:Pamela Ann Carpentier
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依托单位:
Maternal Inflammation Alters Fetal Brain Development via Tumor necrosis Factor-al
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批准号:7694984
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项目类别:
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资助金额:$1.29万
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财政年份:2008
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负责人:Pamela Ann Carpentier
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依托单位:
Astrocytes-Innate & Adaptive Immune Response to Virus
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批准号:6793523
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项目类别:
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资助金额:$3.3万
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财政年份:2004
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负责人:Pamela Ann Carpentier
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依托单位:
海外基金