Discovery of novel immunoevasins from HHV-6 and -7
Discovery of novel immunoevasins from HHV-6 and -7
批准号:
7359231
负责人:
AMY W HUDSON
金额:
$22.42万
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:
2008-06-26 至 2010-05-31
关键词:
AddressAffinity ChromatographyAntigen PresentationAntigen-Presenting CellsAntigensAutoimmune DiseasesBindingCell Adhesion MoleculesCell Culture SystemCell LineCell surfaceCellsCellular MembraneCellular biologyCytomegalovirusCytotoxic T-LymphocytesDetectionDiseaseDown-RegulationDuctalEncephalitisExcisionExpression LibraryGoalsHerpesviridaeHistocompatibility Antigens Class IHuman Herpesvirus 6Human Herpesvirus 7ImmuneImmune responseImmune systemImmunocompromised HostIndividualInfectionKnowledgeLeadLifeLigandsMembrane ProteinsMolecularNatural Killer CellsOpen Reading FramesOpportunistic InfectionsPathogenesisPopulationSalivary GlandsSimplexvirusSurfaceTestingTransplant RecipientsViralViral ProteinsVirusVirus Diseasescell killingnovelpermissivenessreceptorresearch studyresponsesalivary celltherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): HHV-6 and -7 are two closely related 2-herpesviruses that infect over 90% of the population. These opportunistic viruses do not cause serious illness in healthy people, but in immunocompromised individuals, these viruses can reactivate and cause life-threatening encephalitis and CMV disease. Like all other herpesviruses, HHV-6 and -7 persist or remain latent in their hosts throughout life. In so doing, herpesviruses have evolved numerous strategies to escape detection by the immune system. Notably, all of the herpesviruses thus far examined interfere with viral antigen presentation to cytotoxic T lymphocytes (CTLs) by removing class I MHC molecules from the infected cell surface. Clearly, since the herpesviruses have evolved such an extensive array of mechanisms to remove class I MHC molecules from the cell surface, this strategy serves them well. However, when Natural Killer (NK) cells detect an absence of class I MHC molecules on the surface of a cell (i.e., "missing self"), they become activated to kill that cell. The focus of this application is to discover how HHV-6 and -7 evade the NK and CTL cell responses to viral infection. Several strategies will be employed to identify novel viral immunoevasins that allow HHV-6/-7 infected cells to escape detection: 1) we will explore the function of open reading frames within HHV-6 and -7 that have obvious homology to immune molecules. 2) We will screen HHV-6 and -7- infected antigen-presenting cells for the surface downregulation of candidate cellular membrane proteins involved in the initiation of a cytolytic response against an infected cell. The long term goal of this project is to understand the mechanisms by which HHV-6 and -7 evade detection by the immune system. Revelation of the mechanisms by which these opportunistic viruses evade the immune system will not only contribute to the understanding of these viruses and their pathogenesis, but also to the understanding of basic underlying principles of cell biology. Ultimately, the knowledge gained from understanding how these molecules function to subvert the immune response may lead to the identification of potential therapeutic targets for the treatment of these opportunistic infections, as well as for the treatment of autoimmune disorders.
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资助金额:$33.11万
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财政年份:2007
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Mechanisms of immune evasion by HHV-6 and HHV-7 U21
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财政年份:2007
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Mechanisms of immune evasion by HHV-6 and HHV-7 U21
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批准号:7448432
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项目类别:
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资助金额:$33.44万
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财政年份:2007
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负责人:AMY W HUDSON
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依托单位:
MOLECULAR BASIS OF SYNAPTIC VESICLE FORMATION
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财政年份:1998
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负责人:AMY W HUDSON
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MOLECULAR BASIS OF SYNAPTIC VESICLE FORMATION
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批准号:2774511
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项目类别:
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资助金额:$1.46万
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财政年份:1997
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负责人:AMY W HUDSON
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依托单位:
MOLECULAR BASIS OF SYNAPTIC VESICLE FORMATION
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批准号:2873917
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项目类别:
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资助金额:$0.98万
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财政年份:1997
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负责人:AMY W HUDSON
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依托单位:
MOLECULAR BASIS OF SYNAPTIC VESICLE FORMATION
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财政年份:1996
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负责人:AMY W HUDSON
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依托单位:
海外基金