Immunoregulation of Flavivirus Infection
Immunoregulation of Flavivirus Infection
批准号:
6966726
负责人:
Nora E Sarvetnick
金额:
$32.53万
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:
已结题
起止时间:
2005-07-01 至 2007-06-30
关键词:
RNase protection assayT cell receptorWest Nile virusconfocal scanning microscopyflow cytometryhost organism interactionimmune responseimmunoregulationinterleukin 15interleukin 18laboratory mouseleukocyte activation /transformationnatural killer cellspathologic processpolymerase chain reactionreceptor expressionvirus infection mechanismvirus loadvirus replication
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): West Nile virus infection can cause severe debilitating consequences following productive infection. Severe encephalitis can result, which can lead to neurological dysfunction and death. There is no vaccine available, and only symptom-specific treatment following clinical evidence of infection. Immune responses to viral infections involve innate responses initially, which are followed by adaptive responses later. The innate response can modulate both viral clearance as well as pathogenesis of the virus. Indeed some viruses have developed sophisticated abilities to modulate the innate immune response, enhancing their infectivity. Innate responses are also induced following vaccination, due to the adjuvants utilized, and therefore, an understanding of these responses will allow for the development of appropriate vaccination strategies. There are virtually no reports available characterizing the innate immune response to West Nile virus. Therefore, in this revised exploratory R21 application we seek to define critical aspects of the host innate response to West Nile virus. We have chosen the R21 mechanism for several reasons. First, since little is known about the innate response to West Nile Virus, we will need to perform exploratory studies regarding the cell and receptors activated following infection. Secondly, the use of this flavivirus is new in our laboratory and we require support to be able to initiate studies on this important virus within our laboratory. Importantly we have arranged for a strategic collaboration between our laboratory and Dr. Margo Brinton, an established investigator in the West Nile virus field. This collaboration will be critical for our success in these West Nile virus investigations. We propose to test two hypotheses in this revised exploratory R21 application. Firstly, we will test the hypothesis that the NK repertoire is both activated and altered following infection by West Nile virus. Secondly, we will test the hypothesis that NK responses are required for viral clearance, but are also involved in viral pathogenesis. We believe that the information obtained from our studies will highlight the role of NK cells and their receptors in the host response to West Nile virus.
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会议论文
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批准号:8681355
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财政年份:2012
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资助金额:$48.64万
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财政年份:2012
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批准号:8374068
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资助金额:$51.56万
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财政年份:2012
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Mechanistic insights into B7 co-stimulation
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资助金额:$35.01万
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依托单位:
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Functional Tolerance to Islet Allografts
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资助金额:$32.53万
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财政年份:2005
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依托单位:
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依托单位:
海外基金