FASEB SRC on Autoimmunity
FASEB SRC on Autoimmunity
批准号:
9330664
负责人:
Joseph Edgar Craft
金额:
$0.9万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-05-01 至 2018-04-30
关键词:
Anti-Cytokine TherapyApplied ResearchAreaAtherosclerosisAutoimmune DiseasesAutoimmune ProcessAutoimmune ResponsesAutoimmunityAwarenessB cell differentiationB-LymphocytesBasic ScienceBiological Response Modifier TherapyCell physiologyCellsChronicClinicClinicalClinical TrialsCollaborationsCommunicationComorbidityComplexDataDevelopmentDiseaseDrug DesignDrug IndustryEconomicsEnsureEnvironmentEtiologyExposure toFailureFertilizationFutureGenderGeneticGenetic Predisposition to DiseaseGoalsGrowthHealthHealth Care CostsHumanImmersion Investigative TechniqueImmuneImmune systemIncidenceIndustryInflammation MediatorsInflammatoryInflammatory Bowel DiseasesInjuryInstitutesInsulin-Dependent Diabetes MellitusInterleukin-17InvestigationKnowledgeLaboratoriesLocationMalignant NeoplasmsMediatingMediator of activation proteinMetabolicMetabolismMolecularNatureObesityParticipantPathogenesisPathogenicityPathway interactionsPharmacologic SubstancePostdoctoral FellowQuality of lifeRegulationResearchResearch PersonnelRheumatoid ArthritisRoleScheduleScienceScientistSocietiesStressStudentsT-LymphocyteTNF geneTherapeuticTherapeutic InterventionTimeTissuesTranslatingTranslationsTreatment EfficacyUnderrepresented MinorityVocational GuidanceWorkbaseclinically significantcytokinedata exchangedifferentiated B celleffective therapyimmune functionimmunoregulationinsightinterestknowledge translationmeetingsmetabolomemicrobiomenovelnovel strategiesnovel therapeutic interventionnovel therapeuticsplanetary Atmosphereposterspreventprogramsrituximabsuccesssymposiumtherapeutic targettraffickingtranslational scientisttrend
中文摘要
项目总结
英文摘要
PROJECT SUMMARY
There has been enormous growth in the past few years in our understanding of pathogenic mechanisms in
autoimmunity, and a new recognition of the similarities and important differences between different
autoimmune diseases. Examples of rapidly moving areas of research in autoimmunity are the identification and
characterization of new subsets of pathogenic T cells that secrete unique inflammatory mediators and novel
insights into the interface between genetic susceptibility, environmental stress, and the microbiome and
metabolome. These findings have emerged largely from the work of basic scientists, and this FASEB science
conference on Autoimmunity has historically focused on discussion of new findings in basic research in
autoimmunity. However, we believe that it is crucial for basic scientists to establish and maintain connections
to scientists who are working to translate mechanisms into therapeutic targets. For example, the unexpected
efficacy of therapeutic B cell depletion in some autoimmune diseases has prompted intense investigation by
basic scientists into the role of B cells in pathogenic pathways. In a like manner, the understanding of the role
of the microbiome influencing immune regulation has led to the discussion and development of potentially
novel therapeutic strategies for other illness, such as inflammatory bowel disease and rheumatoid arthritis.
Basic information on metabolism in regulatory and effect T cells has spurred interest in the drive toward
metabolic manipulations as therapeutic strategies, not only in cancer, but also in autoimmunity. Therefore,
while maintaining a focus on cutting edge basic research in autoimmunity, we will continue to have as
speakers translational scientists that focus upon mechanisms of tissue injury in human autoimmune diseases,
and that will discuss new strategies for treating autoimmune diseases and current data on the successes and
failures of manipulating the immune system in autoimmune humans. We expect that emphasis on therapeutic
treatment of autoimmune disease will attract both basic and industry scientists, and will stimulate strong
interest among both junior and established investigators. The size and setting of this meeting are ideal to
promote the open exchange of data and cross-fertilization of ideas that will stimulate new hypotheses and
directions in autoimmunity research.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
A novel Lyme disease vaccine
-
批准号:10515700
-
项目类别:
-
资助金额:$64.81万
-
财政年份:2022
-
负责人:Joseph Edgar Craft
-
依托单位:
A novel Lyme disease vaccine
-
批准号:10640164
-
项目类别:
-
资助金额:$64.81万
-
财政年份:2022
-
负责人:Joseph Edgar Craft
-
依托单位:
Human and Translational Immunology Training Program
-
批准号:10649548
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项目类别:
-
资助金额:$42.43万
-
财政年份:2021
-
负责人:Joseph Edgar Craft
-
依托单位:
Human and Translational Immunology Training Program
-
批准号:10270035
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项目类别:
-
资助金额:$42.32万
-
财政年份:2021
-
负责人:Joseph Edgar Craft
-
依托单位:
Human and Translational Immunology Training Program
-
批准号:10474483
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项目类别:
-
资助金额:$44.77万
-
财政年份:2021
-
负责人:Joseph Edgar Craft
-
依托单位:
Pathogenesis of Lupus Nephritis
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批准号:10612792
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项目类别:
-
资助金额:$61.1万
-
财政年份:2020
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负责人:Joseph Edgar Craft
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依托单位:
Pathogenesis of Lupus Nephritis
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批准号:10159199
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项目类别:
-
资助金额:$61.83万
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财政年份:2020
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负责人:Joseph Edgar Craft
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依托单位:
Pathogenesis of Lupus Nephritis
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批准号:10396047
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项目类别:
-
资助金额:$61.1万
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财政年份:2020
-
负责人:Joseph Edgar Craft
-
依托单位:
Follicular Helper T Cell Function in Autoimmunity
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批准号:10320436
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项目类别:
-
资助金额:$29.85万
-
财政年份:2018
-
负责人:Joseph Edgar Craft
-
依托单位:
Follicular Helper T Cell Function in Autoimmunity
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批准号:10061557
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项目类别:
-
资助金额:$32.17万
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财政年份:2018
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负责人:Joseph Edgar Craft
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依托单位:
An in vivo CRISPR-Cas9 genetic screen in murine primary T cells to discover metabolic regulators of follicular B helper T (Tfh) cell differentiation
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批准号:9468613
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项目类别:
-
资助金额:$39.55万
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财政年份:2017
-
负责人:Joseph Edgar Craft
-
依托单位:
An in vivo CRISPR-Cas9 genetic screen in murine primary T cells to discover metabolic regulators of follicular B helper T (Tfh) cell differentiation
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批准号:9553491
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项目类别:
-
资助金额:$41.41万
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财政年份:2017
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负责人:Joseph Edgar Craft
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依托单位:
Cis Regulatory Elements and Systemic Lupus Erythematosus
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批准号:9980291
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项目类别:
-
资助金额:$52.58万
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财政年份:2016
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负责人:Joseph Edgar Craft
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依托单位:
Cis Regulatory Elements and Systemic Lupus Erythematosus
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批准号:9319206
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项目类别:
-
资助金额:$53.93万
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财政年份:2016
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负责人:Joseph Edgar Craft
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依托单位:
Manipulation of Follicular Helper T Cells in Immunity and Autoimmunity
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批准号:8430482
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项目类别:
-
资助金额:$22.42万
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财政年份:2012
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负责人:Joseph Edgar Craft
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依托单位:
A Novel B Cell Marker and Therapeutic Target in Lupus
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批准号:8442322
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项目类别:
-
资助金额:$17.78万
-
财政年份:2012
-
负责人:Joseph Edgar Craft
-
依托单位:
A Novel B Cell Marker and Therapeutic Target in Lupus
-
批准号:8285600
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项目类别:
-
资助金额:$22.39万
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财政年份:2012
-
负责人:Joseph Edgar Craft
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依托单位:
Manipulation of Follicular Helper T Cells in Immunity and Autoimmunity
-
批准号:8541697
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项目类别:
-
资助金额:$17.79万
-
财政年份:2012
-
负责人:Joseph Edgar Craft
-
依托单位:
Dissecting the role for IL-15 in CD8+ T cell homeostasis in human lupus
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批准号:7461237
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项目类别:
-
资助金额:$41.32万
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财政年份:2008
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负责人:Joseph Edgar Craft
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依托单位:
Dissecting the role for IL-15 in CD8+ T cell homeostasis in human lupus
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批准号:8012864
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项目类别:
-
资助金额:$40.55万
-
财政年份:2008
-
负责人:Joseph Edgar Craft
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依托单位:
海外基金