Vitamin D and NKT Cell Regulation of Multiple Sclerosis
Vitamin D and NKT Cell Regulation of Multiple Sclerosis
批准号:
8046295
负责人:
MARGHERITA T CANTORNA
金额:
$31.14万
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 2015-03-31
关键词:
AffectAgeAnti-Inflammatory AgentsAnti-inflammatoryAntigen PresentationAntigensAutoimmune DiseasesAutoimmunityCD8B1 geneCellsCessation of lifeChildChildhoodComplementDataDeveloped CountriesDevelopmentDietDiseaseDoseEnvironmentExperimental Autoimmune EncephalomyelitisExposure toGoalsHomeostasisHumanHygieneImmuneImmune responseImmune systemImmunityIn VitroIncidenceInfantKnockout MiceLifeLinkMediatingMisinformationMolecularMolecular TargetMultiple SclerosisMusPatientsPlayPollutionPopulationPreventionPrincipal InvestigatorPropertyRegulationRegulatory T-LymphocyteRoleSerumShapesStagingSun ExposureT cell responseT-LymphocyteTestingThymus GlandUniversitiesVitamin DVitamin D3 ReceptorVitaminsWorkcellular targetingcytokinedietary supplementsexperiencegastrointestinalimmune functionin uteroin vivoinhibitor/antagonistkiller T cellmicrobialnovelpediatric departmentprenatalpreventprogramspublic health relevanceresponseseason of birththymocyte
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): There are profound effects of vitamin D on immune function. There is data to suggest that increased levels of vitamin D (either through diet, supplements or sunlight exposure) are beneficial for multiple sclerosis (MS) patients. In addition, active vitamin D (1,25(OH)2D3) treatment of experimental autoimmune encephalomyelitis (EAE) blocks the development of disease. In the first year of life infants undergo considerable fluctuation in their circulating vitamin D (25(OH)D3) levels. We hypothesize that early changes in vitamin D have profound effects on the thymus such that iNKT cells fail to develop and as a result autoimmune diseases like MS are more likely to develop. iNKT cells require adequate vitamin D in utero and the expression of the vitamin D receptor (VDR) for both development and function. iNKT cells have been implicated as inhibitors and regulatory cells in EAE and MS. The hypothesis to be tested is that vitamin D regulates iNKT cells and as a result is important for shaping the developing immune response and preventing and controlling the development of autoimmunity. The goals of this proposal are to determine the molecular mechanisms underlying vitamin D and the VDRs effects on iNKT cells. The aims are to determine the plasticity of the iNKT cell response as a function of changes in vitamin D status, determine the role of vitamin D in the thymus for iNKT cell development, determine how changes in vitamin D affect proliferation, survival and death of iNKT cells, and to determine the role of active vitamin D (1,25(OH)2D3) regulation of iNKT cells in suppression of EAE and whether changes in vitamin D status in vivo or 1,25(OH) 2D3 in vitro regulates human NKT cell expansion and function. NKT cells are novel targets in MS and a better understanding of the mechanisms by which their development and function are regulated by vitamin D and 1,25(OH)2D3 would be critical for manipulating NKT cells therapeutically.
PUBLIC HEALTH RELEVANCE: There is at present a great deal of misinformation about vitamin D and vitamin D supplements as immune system modulators in the public forum. Identifying the cellular and molecular targets of vitamin D in the immune system is important so that rational decisions about the use of vitamin D supplements and/or active vitamin D compounds to manipulate the immune system and prevent or treat autoimmune diseases like multiple sclerosis.
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依托单位:
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