Genetic Approaches to the Study of Plasmacytoid Dendritic Cell Function
Genetic Approaches to the Study of Plasmacytoid Dendritic Cell Function
批准号:
7774245
负责人:
Boris Reizis
金额:
$19.67万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-04-01 至 2012-03-31
关键词:
AblationAllelesAllergic inflammationAlloantigenAllograftingAnimal ModelAnimalsAntigensAntiviral AgentsAutoantibodiesAutoantigensAutoimmune DiseasesAutoimmune ProcessAutoimmunityB-LymphocytesCell LineageCell physiologyCellsChronicDataDendritic CellsDendritic cell activationDevelopmentEncephalomyelitisExhibitsGene Expression ProfileGeneticGenetic ModelsGenetic RecombinationGoalsGrowthHumanITGAX geneImmuneImmune responseImmunityInfectionInflammationInsulin-Dependent Diabetes MellitusInterferon Type IInterferonsKnockout MiceLigandsLinkLongitudinal StudiesLupusMediatingModelingMolecularMonitorMouse StrainsMultiple SclerosisMurine hepatitis virusMusOptic NeuritisOralPhenotypePlayPopulationProductionPropertyPsoriasisReactionReportingRoleSeveritiesSpecificitySurfaceSyndromeSystemT cell differentiationT cell responseT-LymphocyteTestingTissuesToll-like receptorsTransgenesViral AntigensVirusVirus Diseasesadaptive immunitycell typefunctional losshuman TLR7 proteinin vivoinsightlupus-likenoveloverexpressionpathogenperipheral tolerancepublic health relevancerelating to nervous systemtooltranscription factor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Plasmacytoid dendritic cells (PDC) represent a unique cell type that plays a critical role in both innate and adaptive immune responses. During viral infection, PDC secrete massive amounts of type I interferon (IFN), as well as present viral antigens and prime T cell responses. In addition to antiviral immunity, PDC have been implicated into many immunological phenomena, including tolerance to oral antigens and allografts, allergic inflammation, antitumor immunity and autoimmunity. In the latter case, PDC were proposed to either promote autoimmune disease through aberrant IFN secretion or counteract it by modulating T cell differentiation. Thus, the precise function of PDC in prolonged immune reactions such as autoimmunity remains to be elucidated. This task calls for the development of novel genetic approaches, such as systems for constitutive PDC lineage ablation. Our lab has recently identified transcription factor E2-2 as a critical regulator of PDC development in mice and humans. We propose to use conditional targeting of E2-2 as a tool for constitutive PDC ablation in the steady state. In Specific Aim 1, E2-2 conditional knockout mice will be characterized for the efficiency and specificity of PDC ablation, and for their IFN secretion capacity and antiviral immune responses. In Specific Aim 2, the resulting "PDC-less" mice will be used to probe the role of PDC in spontaneous animal models of autoimmune neural inflammation and of lupus-like autoimmunity. These studies would generate a novel experimental system for the study of PDC, and provide insights into the role of PDC in autoimmune diseases.
PUBLIC HEALTH RELEVANCE: The study is aimed at the functional analysis of plasmacytoid dendritic cells (PDC), a unique immune cell type that plays a major role in antiviral immunity and other immune responses. The development of a novel genetic model for constitutive PDC ablation would facilitate the study of PDC function and provide insights into the role of PDC in autoimmune diseases such as multiple sclerosis and lupus.
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海外基金