Binding and Presentation of Lipid Antigens by CD1
Binding and Presentation of Lipid Antigens by CD1
批准号:
8295005
负责人:
Steven A Porcelli
金额:
$40.67万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-07-01 至 2014-06-30
关键词:
AdjuvantAgonistAntigen ReceptorsAutoimmune DiseasesAutoimmunityBindingBiochemicalBiological AssayBiological ModelsCD1 AntigensCD8B1 geneCell physiologyCellsChemicalsChemosensitizationCholesterolComplexDetergentsExclusionFractionationGalactosylceramidesGlycolipidsGoalsHealthHumanImageImmune responseImmune systemImmunityImmunotherapeutic agentImmunotherapyInfectionInsulin-Dependent Diabetes MellitusLeadLibrariesLigandsLipidsMaintenanceMalignant NeoplasmsMembrane MicrodomainsMethodsMonoclonal AntibodiesMultiple SclerosisMusPatternPharmaceutical PreparationsPreventionProductionPropertyProteinsReagentRegulationResistanceRoleStructure-Activity RelationshipSystemT cell responseT-LymphocyteT-Lymphocyte SubsetsVaccinationVaccine AdjuvantVaccinesallograft rejectionanalogbasecytokinehuman diseaseimprovedinvariant chainlong term memorymouse modelnovelnovel vaccinespathogenpreventresponsetherapeutic developmenttranslational study
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): T lymphocytes known as type 1 or invariant NKT cells (iNKT cells) recognize specific lipid ligands presented by the CD1d protein, and this component of the CD1-dependent immune response is highly conserved between humans and mice. Many detailed studies in mouse models have shown that iNKT cells contribute to immune responses against pathogens, elimination of malignant tumors, maintenance of immunological tolerance and prevention of autoimmune diseases. Great progress in understanding and potentially harnessing the many immunological activities of iNKT cells has been made in recent years as a result of the identification of various forms of synthetic a-galactosylceramide (aGalCer) that specifically activate these cells. The current proposal is focused on the identification of modified forms of aGalCer that activate different cytokine patterns when used to stimulate mouse or human iNKT cells. Numerous Th2-cytokine biasing forms of aGalCer have been identified in our ongoing studies, and we propose new synthetic approaches to create additional aGalCer analogues that will include examples with tolerogenic or proinflammatory activities based on cytokine production or other effects. These compounds will be characterized in detail using assay systems to analyze both mouse and human iNKT cell responses to identify those that are most suitable to carry forward into translational studies. Using new monoclonal antibody reagents specific for CD1d/aGalCer complexes, and soluble iNKT cell antigen receptors, we will carry out a range of studies to determine the mechanisms that lead to the stimulation of markedly different patterns of cytokines by various aGalCer analogues. Studies to optimize the adjuvant properties of selected aGalCer analogues in model systems of vaccination are also proposed. These studies will increase our understanding of the mechanisms governing the regulation of the many potential activities of iNKT cells, and will contribute to development of therapeutic applications for glycolipid activators of this T cell subset. PUBLIC HEALTH RELEVANCE: This project will develop chemical compounds that specifically activate a specialized subset of T lymphocytes known as iNKT cells. These T cells have the ability to either stimulate or suppress immune responses, depending on how they are activated. The studies put forth in this proposal will identify compounds that selectively activate either the stimulatory or suppressive functions of iNKT cells, which will lead to the ability to more precisely control the functions of these cells for the prevention or treatment of human disease. The potential range of applications for iNKT cell activators is very broad and includes their use as drugs for prevention of autoimmune diseases such as type 1 diabetes or multiple sclerosis, as well as their incorporation into new vaccines for infections and cancer.
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会议论文
Flow Cytometery and Cell Sorting Core
-
批准号:10659181
-
项目类别:
-
资助金额:$21.09万
-
财政年份:2022
-
负责人:Steven A Porcelli
-
依托单位:
Flow Cytometery and Cell Sorting Core
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批准号:10408970
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项目类别:
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资助金额:$21.52万
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财政年份:2022
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负责人:Steven A Porcelli
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依托单位:
Bigfoot Multispectral High Speed Fluorescence Activated Cell Sorter
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批准号:10414835
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项目类别:
-
资助金额:$60.0万
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财政年份:2022
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负责人:Steven A Porcelli
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依托单位:
"Determinants of T Cell Immunity to Tuberculosis Vaccines"
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批准号:8871648
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项目类别:
-
资助金额:$7.17万
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财政年份:2015
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负责人:Steven A Porcelli
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依托单位:
Flow Cytometry Core
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批准号:8871652
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项目类别:
-
资助金额:$2.34万
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财政年份:2015
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负责人:Steven A Porcelli
-
依托单位:
Construction of safe and effective live tuberculosis vaccines
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批准号:8230473
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项目类别:
-
资助金额:$41.5万
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财政年份:2011
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负责人:Steven A Porcelli
-
依托单位:
Defining the Correlates of Bactericidal Immunity in Tuberculosis
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批准号:8031491
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项目类别:
-
资助金额:$24.9万
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财政年份:2011
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负责人:Steven A Porcelli
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依托单位:
Construction of safe and effective live tuberculosis vaccines
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批准号:8626351
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项目类别:
-
资助金额:$41.5万
-
财政年份:2011
-
负责人:Steven A Porcelli
-
依托单位:
"Determinants of T Cell Immunity to Tuberculosis Vaccines"
-
批准号:8049854
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项目类别:
-
资助金额:$37.35万
-
财政年份:2011
-
负责人:Steven A Porcelli
-
依托单位:
Construction of safe and effective live tuberculosis vaccines
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批准号:8083413
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项目类别:
-
资助金额:$41.5万
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财政年份:2011
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负责人:Steven A Porcelli
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依托单位:
Flow Cytometry Core
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批准号:8049861
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项目类别:
-
资助金额:$19.94万
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财政年份:2011
-
负责人:Steven A Porcelli
-
依托单位:
Defining the Correlates of Bactericidal Immunity in Tuberculosis
-
批准号:8207834
-
项目类别:
-
资助金额:$20.81万
-
财政年份:2011
-
负责人:Steven A Porcelli
-
依托单位:
Construction of safe and effective live tuberculosis vaccines
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批准号:8431439
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项目类别:
-
资助金额:$39.01万
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财政年份:2011
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负责人:Steven A Porcelli
-
依托单位:
Construction of safe and effective live tuberculosis vaccines
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批准号:9132485
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项目类别:
-
资助金额:$19.09万
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财政年份:2011
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负责人:Steven A Porcelli
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依托单位:
Flow Cytometry Core
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批准号:7943653
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项目类别:
-
资助金额:$2.84万
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财政年份:2010
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负责人:Steven A Porcelli
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依托单位:
Digital Extra Parameter (DxP8)
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批准号:7794342
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项目类别:
-
资助金额:$11.96万
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财政年份:2010
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负责人:Steven A Porcelli
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依托单位:
Laser Scanning Cytometer
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批准号:7595975
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项目类别:
-
资助金额:$39.84万
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财政年份:2008
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负责人:Steven A Porcelli
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依托单位:
MoFlow High Speed Fluorescence Activated Cell Sorter
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批准号:7213177
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项目类别:
-
资助金额:$43.16万
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财政年份:2007
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负责人:Steven A Porcelli
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依托单位:
FLOW CYTOMETRY SHARED RESOURCE
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批准号:7506847
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项目类别:
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资助金额:$13.83万
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财政年份:2007
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负责人:Steven A Porcelli
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依托单位:
Prevention of Diabetes with Lipid Immunomodulators
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批准号:6827496
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项目类别:
-
资助金额:$22.96万
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财政年份:2004
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负责人:Steven A Porcelli
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依托单位:
国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
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批准号:32000851
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项目类别:青年科学基金项目
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资助金额:24.0万元
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批准年份:2020
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负责人:乔安娜
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依托单位: