Novel IFN - Dependent Innate Antiviral Mechanisms
Novel IFN - Dependent Innate Antiviral Mechanisms
批准号:
7641550
负责人:
HERBERT W VIRGIN
金额:
$45.08万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-03-01 至 2009-02-28
关键词:
AntigensAntiviral AgentsBinding ProteinsBiologicalBiological AssayCellsClassCollaborationsCoupledDNA VirusesDataDengueDiamondGene ChipsGenesGoalsGrantHybridsImmunityInfectionInterferonsLeadLearningMapsMethodsMicroarray AnalysisMolecularMouse Pox VirusMusNumbersPhysiologicalPlayProteinsRNARepressionResistanceRoleSaintsSorting - Cell MovementTestingUbiquitin Like ProteinsUniversitiesVaccinesVaccinia Virus StudyViralViral ProteinsVirusVirus DiseasesWest Nile virusWorkYeastsbasecytokineexpression cloninggene functionimmune functionin vivonovelvector
中文摘要
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英文摘要
Interferons (IFNs) play a critical role in innate defense against infection with RNA and DNA viruses.
A detailed understanding of how these critical cytokines inhibit viral infection might lead to pharmacologic
approaches to induce resistance to multiple potentially dangerous agents without the necessity of inducing
prior antigen-specific immunity. Given the large number of potential biological weapons for which no
vaccine exists, this is an important goal. IFNs work via induction or repression of proteins that interfere with
viral replication or alter the function of immune cells. In this grant we will focus on IFN regulated genes that
inhibit viral replication. There are hundreds of IFN regulated genes, the function of only a few of which is
understood in detail. Sorting through the many IFN regulated genes to find those with specific antiviral
functions is a daunting task. Our preliminary data, and work from others, suggests that critically important
IFN inducible antiviral molecules remain unidentified. We have succeeded in developing methods for
discovering these important antiviral molecules.
Based on these considerations, we propose to identify and analyze the mechanisms of action of novel
IFN induced antiviral proteins. We will use two screens for antiviral proteins: (i) expression cloning of
proteins that block viral replication, and (ii) use of gene chip analysis coupled to a Sindbis vector based
complementation assay to identify proteins with antiviral function in vivo. We have successfully used this
second approach to identify an IFN inducible antiviral protein, the ubiquitin-like protein ISG15. We have
begun to analyze the role of ISG15 in resistance to several viruses including viruses in Class A and B. In this
proposal we will analyze ISG 15 action in infected cells in detail (Aim 1), and continue to use the screens we
have set up to identify additional novel IFN induced antiviral molecules (Aim 2).
Aim 1. Determine the molecular mechanism(s) of the antiviral effect of ISG15.
Aim 2. Identify candidate novel antiviral proteins and prove their physiologic relevance.
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财政年份:2014
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财政年份:2011
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资助金额:$68.19万
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财政年份:2011
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依托单位:
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海外基金