ADMINISTRATIVE CORE, CENTER DIRECTOR, ENRICHMENT PROGRAM
ADMINISTRATIVE CORE, CENTER DIRECTOR, ENRICHMENT PROGRAM
批准号:
8015122
负责人:
Ramnik J Xavier
金额:
$78.38万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
Academic Medical CentersAllelesAnimal ModelAntigen-Presenting CellsArchitectureArtsAutophagocytosisAwardB-LymphocytesBioinformaticsBiologicalBiologyBostonCell physiologyCellsClinicalClinical TrialsColitisCollaborationsCommunitiesComplex Genetic TraitCrohn&aposs diseaseDevelopmentDigestive System DisordersDiseaseDisease modelDisease susceptibilityDissectionDrug Delivery SystemsEngineeringEpidemiologistEpithelialEpithelial CellsEpitheliumEquilibriumFCGR2A geneFundingGene ChipsGeneral HospitalsGenesGeneticGenetic ResearchGenomicsGoalsGrantHealthHuman GeneticsImmuneImmune responseImmune systemImmunologistIndividualInflammationInflammation MediatorsInflammatoryInflammatory Bowel DiseasesInflammatory ResponseInflammatory disease of the intestineInstitutesInterleukin-10InterventionIntestinal MucosaIntestinesIsraelKnowledgeLaboratoriesLymphocyteLymphocyte ActivationLymphocyte antigenMassachusettsMedical centerMicrobeModelingMolecularMolecular BiologyMucous MembraneNatural ImmunityPathogenesisPathway interactionsPatientsPenetrationPhagocytosisPhenotypePhysiologicalPopulationPositioning AttributePredispositionProcessRegulationRegulatory T-LymphocyteResearchResearch PersonnelResearch SupportRiskRoleRunningServicesSurfaceTechnologyTissuesTranslationsUlcerative ColitisUnited Statesadaptive immunityarmbasecohortcomputerized toolscytokinegenome wide association studyinsightinterleukin-23knowledge basemacrophagemembermicroorganism interactionmouse modelnovelnovel strategiespreventprogramsresponsetheoriestool
中文摘要
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英文摘要
Overview
Understanding the pathogenesis of Inflammatory Bowel Diseases (IBD) represents one of the most important and unresolved challenges in both clinical and investigative digestive diseases. As a result of research advances over the past several years, including many made possible by this Center, it is now possible to formulate a central hypothesis for the pathogenesis of these disorders and to apply powerful new tools that will facilitate further advances in the next several years.
The many novel aspects of our understanding of the multiple pathwavs to ulcerative colitis (UC) and Crohn's disease (CD) are based upon a comprehensive dissection of the manv complexities of mucosal biology. These advances are also based on knowledge of factors sustaining surface epithelial integrity, innate immunity, lymphocyte activation, host-microbe interaction, genetic architecture of Crohn's disease and ulcerative colitis, and functional characterization of lymphocytes and antigen presenting cell populations in the intestinal mucosa.
Since the last competing application, the participating collaborating investigators in this Center for the Study of IBD (CSIBD) have made many key advances in the understanding of the processes relevant to IBD and catalyzed by CSIBD, have increased their research support. The CSIBD has achieved its original goals, primarily by expanding the infrastructural support available to a cohort of highly productive investigators, and by offering, through the awarding of pilot feasibility grants, opportunities for the initiation of new ventures in inflammatory bowel disease-related research aimed primarily at young investigators.
The current proposal reflects the conviction of members of the research community at the Massachusetts General Hospital (MGH), the Beth Israel Deaconess Medical Center (BIDMC), the Massachusetts Institute of Technology (MIT), the Broad Institute of Harvard and MIT and the Tufts University Medical Center that they remain in an outstanding position to achieve integration of a broad base of investigators who study basic processes of innate and adaptive immune responses, inflammatory mediators, epithelial cell function and mucosal-microbial interaction. Specifically, Center investigators are well-positioned in the coming period to undertake novel approaches, as the CSIBD has recently initiated a collaboration with the Broad Institute that will allow CSIBD investigators access to a wide array of Broad research platforms in addition to Core services.
The need for Pilot Feasibility Support (PFS) by the Boston-Cambridge IBD research communities is unabated, as evidenced by the number of applications per cycle. The Center Centers have been upgraded to offer stateof-the-art computational tools and bioinformatics support, in the coming period. Gene chip technology has now moved on from microarray to so-called deep sequencing which will be offered in the Genetics, Genomics and Molecular Biology Core both in the MGH setting and for selected projects at the Broad Institute Platform. A major focus of the next funding period will be the clinical translation of human genetics research to understand biological predisposition, to dissect biological pathways that mark disease and identify targets for drug intervention. Investigators are exploring alterations of these processes in both animal models of intestinal inflammation as well as in patients with IBD. We believe that this Center for the Study of Inflammatory Bowel Disease (CSIBD) will continue to provide a highly effective framework for promoting these interactions and a mechanism for the interface of the research community with both powerful new tools for IBD research and a large clinical investigation, patient and tissue base.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Cardiovascular disease, metabolic syndrome, microbes and metabolites in FHS
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批准号:10367105
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项目类别:
-
资助金额:$99.11万
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财政年份:2022
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负责人:Ramnik J Xavier
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依托单位:
Cardiovascular disease, metabolic syndrome, microbes and metabolites in FHS
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批准号:10556439
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项目类别:
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资助金额:$95.59万
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财政年份:2022
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负责人:Ramnik J Xavier
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依托单位:
Core 2: Immune Bioinformatics and Computational Biology Core
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批准号:10251175
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项目类别:
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资助金额:$16.62万
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财政年份:2019
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负责人:Ramnik J Xavier
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依托单位:
Core 2: Immune Bioinformatics and Computational Biology Core
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批准号:10020930
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项目类别:
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资助金额:$18.11万
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财政年份:2019
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负责人:Ramnik J Xavier
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依托单位:
RP2: Targeting genes and pathways for autophagy-dependent inhibition of bacterial infection
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批准号:10364724
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项目类别:
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资助金额:$135.5万
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财政年份:2019
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负责人:Ramnik J Xavier
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依托单位:
RP2: Targeting genes and pathways for autophagy-dependent inhibition of bacterial infection
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批准号:10573259
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项目类别:
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资助金额:$141.17万
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财政年份:2019
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负责人:Ramnik J Xavier
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依托单位:
Functional characterization of CARD9 genetic variants in fungal immunity
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批准号:10331807
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项目类别:
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资助金额:$69.83万
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财政年份:2018
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负责人:Ramnik J Xavier
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依托单位:
Center for the Study of Inflammatory Bowel Disease at Massachusetts General Hospital
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批准号:9262326
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项目类别:
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资助金额:$6.21万
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财政年份:2016
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负责人:Ramnik J Xavier
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依托单位:
Bacterial Dysbiosis in IgG4-RD
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批准号:8732925
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项目类别:
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资助金额:$10.85万
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财政年份:2014
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负责人:Ramnik J Xavier
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依托单位:
ATG16L1 T300A: genetics to biology
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批准号:8588317
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项目类别:
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资助金额:$47.43万
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财政年份:2013
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负责人:Ramnik J Xavier
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依托单位:
ATG16L1 T300A: genetics to biology
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批准号:8421941
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项目类别:
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资助金额:$47.64万
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财政年份:2013
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负责人:Ramnik J Xavier
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依托单位:
Analysis of autophagy risk genes in inflammation and tissue homeostasis
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批准号:9906895
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项目类别:
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资助金额:$54.74万
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财政年份:2013
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负责人:Ramnik J Xavier
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依托单位:
Autophagy genes and the microbiome in Crohn's Disease
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批准号:8295619
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项目类别:
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资助金额:$69.38万
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财政年份:2012
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负责人:Ramnik J Xavier
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依托单位:
Autophagy genes and the microbiome in Crohn's Disease
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批准号:8539596
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项目类别:
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资助金额:$62.42万
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财政年份:2012
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负责人:Ramnik J Xavier
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依托单位:
Autophagy genes and the microbiome in Crohn's Disease
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批准号:8729483
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项目类别:
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资助金额:$63.73万
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财政年份:2012
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负责人:Ramnik J Xavier
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依托单位:
Bioinformatics Core
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批准号:8196497
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项目类别:
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资助金额:$15.33万
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财政年份:2011
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负责人:Ramnik J Xavier
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依托单位:
Center for the Study of Inflammatory Bowel Disease
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批准号:8075186
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项目类别:
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资助金额:$50.8万
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财政年份:2010
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负责人:Ramnik J Xavier
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依托单位:
Genomic Approaches to Host-Pathogen Interactions
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批准号:7476273
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项目类别:
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资助金额:$33.34万
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财政年份:2006
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负责人:Ramnik J Xavier
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依托单位:
Genomic Approaches to Host-Pathogen Interactions
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批准号:7263927
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项目类别:
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资助金额:$33.99万
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财政年份:2006
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负责人:Ramnik J Xavier
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依托单位:
Genomic Approaches to Host-Pathogen Interactions
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批准号:7030660
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项目类别:
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资助金额:$34.45万
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财政年份:2006
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负责人:Ramnik J Xavier
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依托单位:
海外基金