Mechanisms and consequences of iNKT cell anergy
Mechanisms and consequences of iNKT cell anergy
批准号:
7890420
负责人:
Luc Van Kaer
金额:
$37.27万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-01 至 2012-07-31
关键词:
AllergicAntigensAtherosclerosisAutoimmune ProcessBackBiochemicalCell LineageCellsCellular biologyDevelopmentDiseaseExperimental ModelsFoundationsFreund&aposs AdjuvantGalactosylceramidesGenerationsGlycolipidsGoalsHealthHumanImmune responseImmune systemImmunotherapyInfectionInflammatoryInsulin-Dependent Diabetes MellitusKnowledgeLaboratoriesLipopolysaccharidesListeria monocytogenesLong-Term EffectsLupusMaintenanceMajor Histocompatibility ComplexMalignant NeoplasmsMeasuresMultiple SclerosisMusNatural Killer CellsPhenotypePlayPreventiveProcessProductionProteinsPublic HealthPublishingRoleSignal TransductionSignaling ProteinSurfaceT cell anergyT cell responseT-Cell ReceptorT-LymphocyteT-Lymphocyte SubsetsTestingTherapeuticVaccine TherapyWorkalpha-galactosylceramideanergybasecell typecytokinefeedinghuman diseasein vivoinsightkiller T cellnovelpreventprogramsprophylacticreceptorresponsetranscription factorubiquitin ligase
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Invariant natural killer T (iNKT) cells are a subset of T lymphocytes that recognize glycolipid antigens presented by the MHC class l-related protein CD1d. Emerging evidence indicates that iNKT cells play a regulatory role in the immune system. The long-term goal of this proposal is to obtain a better understanding of the in vivo immune response of mice to various stimulators of iNKT cells and to utilize this information for the development of better prophylactic and therapeutic approaches of human disease. Studies from our laboratory have demonstrated that the prototypical iNKT cell antigen, alpha-galactosylceramide (GalCer) can prevent disease in experimental models of type 1 diabetes, multiple sclerosis and lupus. Despite the impact of GalCer treatment on a variety of disease processes, our understanding of the response of iNKT cells themselves to glycolipid antigens is limited. Recent studies from our laboratory have demonstrated that the response of iNKT cells to GalCer activation is characterized by surface receptor down-modulation, expansion, cytokine production, cross-talk with other cells, homeostatic contraction, and acquisition of an anergic phenotype. Guided by these preliminary findings, our proposed studies will test the overall hypothesis that glycolipid activation of iNKT cells initiates a program of anergy induction with long-term effects on subsequent iNKT cell-controlled immune responses. We will test this hypothesis in three integrated Specific Aims: Aim 1 will determine the cellular interactions that are critical for the induction and maintenance of long-term iNKT cell anergy, Aim 2 will investigate the biochemical mechanisms involved in the induction and maintenance of iNKT cell anergy, and Aim 3 will evaluate the long-term effects of iNKT cell unresponsiveness to the subsequent generation of iNKT cell-controlled immune responses. Completion of the work described in this proposal will provide novel insight into fundamental iNKT cell biology, the response of iNKT cells to glycolipid antigens, and the immunomodulatory activities of iNKT cells during health and disease. These proposed studies will build a foundation of knowledge on which safe and effective iNKT cell-based vaccines and therapies can be established. Relevance to Public Health: Studies proposed in this application will contribute significantly to the development of better preventive measures and therapies of infections, cancers, and autoimmune (e.g., type 1 diabetes, multiple sclerosis and lupus), allergic and inflammatory (e.g., atherosclerosis) diseases.
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会议论文
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批准号:7784037
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批准号:8292204
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Glycolipid-Reactive NKT Cells, Obesity and Insulin Resistance
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批准号:8501435
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资助金额:$30.92万
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