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FASEB SRC on Autoimmunity

FASEB SRC on Autoimmunity
关于自身免疫的 FASEB SRC
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

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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.
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