Metabolic regulation of T cell fate and tumor immunity
Metabolic regulation of T cell fate and tumor immunity
批准号:
8438304
负责人:
Fan Pan
金额:
$38.07万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-11-15 至 2017-10-31
关键词:
AddressAffectAnti-Inflammatory AgentsAnti-inflammatoryAntibodiesAutoantigensAutoimmune DiseasesAutoimmunityAutomobile DrivingCancer ModelCell LineageCell MaintenanceCell physiologyCellsChIP-seqChronicClinicalClinical TrialsColitisColon CarcinomaCoupledCuesDataDevelopmentDigoxinDiseaseEctopic ExpressionElementsEnvironmentEquilibriumFutureGenesGrowthGrowth and Development functionHealthHumanIL2RA geneImmuneImmune responseImmunityImmunotherapyIn VitroIndiumInflammationInflammatory disease of the intestineInterleukin-17IntestinesMaintenanceMalignant NeoplasmsMediatingMetabolicMetabolismModelingMusNatureOrganismPathologyPathway interactionsPhenotypePlayPopulationProcessProductionRegulationReporterReportingResearchRoleSignal TransductionSupporting CellSystemT cell differentiationT cell regulationT cell responseT-LymphocyteT-Lymphocyte SubsetsTestingTherapeuticTouch sensationTransgenic MiceTumor AntigensTumor ImmunityUp-RegulationWorkbasecancer immunotherapycancer typecarcinogenesiscommensal microbesefficacy testingflexibilityhypoxia inducible factor 1in vivoinhibiting antibodyinhibitor/antagonistmelanomametabolic abnormality assessmentnovelpathogenpublic health relevanceresearch clinical testingresponsesmall moleculesubcutaneoussuccesstherapeutic targettranscription factortreatment strategytumortumor growthtumor initiationtumor microenvironmenttumor progressiontumorigenesis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Immunotherapy, which focuses on augmenting host immunity against tumor-associated antigens, represents an important means to treat cancer that is yielding clinical success. Successful manipulation of T cell responses requires understanding how particular T cell subsets influence cancer development and growth. For example, Th1 and Th17 cells can augment tumorigenesis. Treg cells can block anti-tumor immune responses and thus represents one of the main obstacles to successful tumor immunotherapy. While Tregs are recognized as tumor supporting cells, the relationship between Th17 cells and tumor immunity has been controversial.
A major unappreciated element in T cell fate decisions is the metabolic environment. As part of an effort to study the metabolic regulation of T cell differentiation decisions, we have discovered that hypoxia inducible factor 1 (HIF-1) plays a critical role in driving the Th17 response. Further preliminary results suggest that lack of this molecule results in reduced tumor initiation and progression. In this proposal, we aim to: (1) further dissect the role of HIF-1 in Th17 development. We will address the breadth, and particular facets of HIF-1's contribution to the Th17 lineage. We will also touch on the suitability of HIF-1 as a therapeutic target in humans; (2) we will explore the role of HIF-1 in regulating the Th17 and Treg responses in inflammation-induced carcinogenesis and cancer progression; (3) we will subsequently use these in vivo cancer models to test the therapeutic potential of HIF-1 targeting. In these studies mice will be treated with the HIF-1 inhibitors, Digoxin and Acriflavine and we will evaluate the ability of these compounds to impede tumor growth either alone or in concert with Treg depletion. Such a strategy is expected to have potent anti-tumor effects as it should, given our preliminary data and past results, simultaneously sabotage two major tumor- promoting immune cell populations
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Metabolic regulation of T cell fate and tumor immunity
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批准号:8581340
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项目类别:
-
资助金额:$40.5万
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财政年份:2012
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负责人:Fan Pan
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依托单位:
Metabolic regulation of T cell fate and tumor immunity
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批准号:8957907
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项目类别:
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资助金额:$40.5万
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财政年份:2012
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负责人:Fan Pan
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依托单位:
Metabolic regulation of T cell fate and tumor immunity
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批准号:9171364
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项目类别:
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资助金额:$40.5万
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财政年份:2012
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负责人:Fan Pan
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依托单位:
海外基金