Epithelial BAFF and APRIL in Airway Inflammation, Immunity and Disease
Epithelial BAFF and APRIL in Airway Inflammation, Immunity and Disease
批准号:
7318283
负责人:
Robert P Schleimer
金额:
$37.75万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-06-01 至 2012-05-31
关键词:
AllergensAllergicAllergic rhinitisAmbrosiaAnti-Inflammatory AgentsAnti-inflammatoryAntigensAppearanceAspergillus fumigatusAsthmaAutoimmune ResponsesAutopsyB cell differentiationB-Cell ActivationB-LymphocytesBiological AssayBiologyBiopsyBone MarrowCell MaturationCell physiologyCellsChronicChronic Obstructive Airway DiseaseClinicalClinical ResearchCollaborationsCollecting CellConditionCytokine ReceptorsDataDiseaseDouble-Stranded RNAEndopeptidasesEngineeringEnzyme ActivationEnzyme TestsEnzyme-Linked Immunosorbent AssayEnzymesEpithelialEpithelial CellsEpitheliumEventExposure toFamily memberGenerationsGoalsHealthHost Defense MechanismHumanIgEImmuneImmune responseImmunityImmunoglobulin AImmunoglobulin Class SwitchingImmunoglobulin GImmunoglobulin IsotypesImmunoglobulin Switch RecombinationImmunoglobulinsImmunohistochemistryImmunologic Deficiency SyndromesIn SituIn VitroInfectionInflammatoryInflammatory ResponseKnock-outLigandsLungLymphoid TissueMature B-LymphocyteMediatingModelingMonitorMouse StrainsMucous MembraneMusMyeloid CellsNoseOperative Surgical ProceduresOrganismPatientsPeptide HydrolasesPharmaceutical PreparationsPlayPollenPolymerase Chain ReactionProcessProductionProtease InhibitorProtein OverexpressionProtocols documentationPulmonary EmphysemaRegulationResearch PersonnelRestRhinitisRoleSamplingSeasonsSeveritiesSignal TransductionSinusSourceSterilityStimulusStructureSystemTALL-1 proteinTLR3 geneTNF geneTestingTimeTissuesTranscriptTransgenic MiceTransgenic OrganismsUpper armVirus DiseasesWestern Blottingactivation-induced cytidine deaminaseairborne allergenairway epitheliumairway inflammationairway obstructionantigen challengebasecell motilityconceptcytokineeosinophilfollow-uphuman diseasehuman subjectin vivoinhibitor/antagonistlaser capture microdissectionmast cellmouse modelpathogenprogramsreceptorresearch studyresponserhinosinusitis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of the project is to test the hypothesis that expression of the TNF family members BAFF and APRIL is important in the local immune and inflammatory responses that occur in the airways in health and disease. These factors are known to cause the proliferation, differentiation and immunoglobulin class switch recombination (CSR) of B lymphocytes. While it has been known for decades that B lymphocytes secrete immunoglobulins locally in the mucosae, until recently it was believed that the process of differentiation and CSR occurred in lymphoid tissues prior to B cell migration to the tissue. Several recent studies support the concept that these events occur extensively in the airways, although the local mechanism is not known. We have made the exciting finding that epithelial cells produce large quantities of BAFF and APRIL, and that BAFF is expressed in chronic rhinosinusitis (CRS) and allergen challenge models in humans, raising the hypothesis that epithelium plays a role in regulation of B cell responses in the airways. We propose experiments to test this hypothesis, using in vivo and in vitro approaches. Studies in Aim 1 will use an explant model to study the production and source of BAFF and APRIL by antigen challenged human mucosal tissue and will analyze the furin proteases involved in their expression. Studies in Aim 2 will test the role of BAFF and APRIL in human diseases, including rhinitis (in collaboration with Dr. Stephen Durham), COPD (in collaboration with Dr. James Hogg), asthma and CRS (in collaboration with investigators at Northwestern), using assays for the presence of these cytokines as well as assays to detect the local presence of B cells and the process of CSR (germline, circle and mature immunoglobulin transcripts and the necessary enzyme activation induced cytidine deaminase). In collaboration with Drs. Charles and Fabienne Mackay, studies in Aim 3 will use mouse models of systemic and airway sensitization and challenge with antigen, and challenge with RSV, to test the role of BAFF and APRIL in B cell responses in the airways. These studies will utilize assays for local B cell responses and inflammatory responses. Studies with knockout and transgenic mice will help pinpoint the cytokine and receptors responsible for important findings. We believe that the proposed studies have direct relevance in the mechanisms of host defense to pathogens and inflammatory airways diseases. Lay description: These studies will test new ideas about how our lungs and nose protect us from infections. We will also study what causes sinus disease, emphysema and asthma. We are testing the importance of two new factors called BAFF and APRIL in immunity and disease.
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批准号:10458540
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项目类别:
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资助金额:$49.05万
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财政年份:2019
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负责人:Robert P Schleimer
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依托单位:
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资助金额:$11.36万
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资助金额:$49.5万
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依托单位:
Chronic Rhinosinusitis Integrative Studies Program 2 (CRISP2)
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资助金额:$183.38万
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财政年份:2019
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依托单位:
Population-based CRS epidemiology: sex differences, natural history, and long-term outcomes based on clinically-defined phenotypes and biologically-based endotypes - Geisinger
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批准号:10458542
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项目类别:
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资助金额:$55.04万
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负责人:Robert P Schleimer
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依托单位:
Population-based CRS epidemiology: sex differences, natural history, and long-term outcomes based on clinically-defined phenotypes and biologically-based endotypes - Geisinger
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批准号:10225451
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项目类别:
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资助金额:$55.55万
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依托单位:
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项目类别:
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资助金额:$49.66万
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Administrative Core
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Administrative Core
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资助金额:$11.38万
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依托单位:
Chronic Rhinosinusitis Integrative Studies Program 2 (CRISP2)
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批准号:9793788
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项目类别:
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依托单位:
Initiators, biomarkers and mechanisms of epithelial dysfunction and immune pathogenesis in chronic rhinosinusitis and aspirin exacerbated respiratory disease (AERD)
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批准号:10083174
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项目类别:
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资助金额:$61.23万
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依托单位:
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项目类别:
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依托单位:
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依托单位:
Chronic Rhinosinusitis Integrative Studies Program (CRISP)
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项目类别:
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财政年份:2013
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负责人:Robert P Schleimer
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海外基金