grant

Core B Clinical Core

Organization UNIVERSITY OF ARIZONALocation TUCSON, UNITED STATESPosted 1 Jun 2016Deadline 31 May 2027
NIHUS FederalResearch GrantFY20252019 novel corona virus2019 novel coronavirus2019-nCoVACE2AllelesAllelomorphsAllergic DiseaseAlveolar MacrophagesAnimal ModelAnimal Models and Related StudiesAnionsAsthmaAtopic AllergyAttenuatedB cell differentiation factorB cell stimulating factor 2B-Cell Differentiation FactorB-Cell Differentiation Factor-2B-Cell Stimulatory Factor-2BCDFBSF-2BSF2BiologicalBiological MarkersBiological Response ModifiersBiometricsBiometryBiomodulatorsBiopsyBiostatisticsBloodBlood Reticuloendothelial SystemBody TissuesBronchial AsthmaBronchoalveolar Lavage FluidBronchoscopyBronchoscopy with Bronchoalveolar LavageBrush CellCOVID-19 infectionCOVID-19 virusCOVID-19 virus infectionCOVID19 infectionCOVID19 virusCell BodyCell Communication and SignalingCell SignalingCellsClinicalClinical DataClinical ResearchClinical StudyCoV-2CoV2CollaborationsCollectionConsentDNADataData AnalysesData AnalysisData CollectionDeoxyribonucleic AcidEffectivenessEpithelial CellsEpitheliumFutureGene TranscriptionGenetic TranscriptionGenotypeGlycerol PhosphoglyceridesGoalsGrippeHPGFHepatocyte-Stimulating FactorHeterogeneityHumanHuman Subject ResearchHybridoma Growth FactorIFN-beta 2IFNB2IL-6IL6 ProteinImmune MediatorsImmune Mediators/ModulatorsImmune RegulatorsImmune responseImmunologic FactorsImmunological FactorsImmunomodulatorsIndividualInfectionInflammationInflammatory ResponseInfluenzaInfluenza AInfluenza A virusInfluenza VirusInfluenza Viruses Type AInfluenzavirus AInnate Immune SystemInnate ImmunityInositide PhospholipidsInositol PhosphoglyceridesInositol PhospholipidsInterleukin-6Intracellular Communication and SignalingInvestigatorsLeadershipLipidsLiquid substanceLung Function TestsMGI-2MediatorModelingModern ManMolecularMyeloid Differentiation-Inducing ProteinNasalNasal EpitheliumNasal Passages NoseNative ImmunityNatural ImmunityNon-Specific ImmunityNonspecific ImmunityNoseOrthomyxovirus Type AParticipantPatient RecruitmentsPatientsPeripheralPhasePhenotypePhosphatidyl InositolPhosphatidylglycerolsPhosphatidylinositolsPhosphoinositidesPlasmacytoma Growth FactorProceduresProcessProductionProtocolProtocols documentationPtdInsPulmonary MacrophagesPulmonary Surfactant-Associated Protein APulmonary function testsRNA ExpressionReceptor ProteinReceptor-Interacting ProteinResearchResearch PersonnelResearch SpecimenResearchersRespiratory EpitheliumRespiratory System, Nose, Nasal PassagesRhinovirusSARS corona virus 2SARS-CO-V2SARS-COVID-2SARS-CoV-2SARS-CoV-2 infectionSARS-CoV2SARS-CoV2 infectionSARS-associated corona virus 2SARS-associated coronavirus 2SARS-coronavirus-2SARS-related corona virus 2SARS-related coronavirus 2SARSCoV2SP-A ProteinSafetySamplingServicesSevere Acute Respiratory Coronavirus 2Severe Acute Respiratory Distress Syndrome CoV 2Severe Acute Respiratory Distress Syndrome Corona Virus 2Severe Acute Respiratory Distress Syndrome Coronavirus 2Severe Acute Respiratory Syndrome CoV 2Severe Acute Respiratory Syndrome-associated coronavirus 2Severe Acute Respiratory Syndrome-related coronavirus 2Severe acute respiratory syndrome associated corona virus 2Severe acute respiratory syndrome coronavirus 2Severe acute respiratory syndrome coronavirus 2 infectionSevere acute respiratory syndrome related corona virus 2Signal TransductionSignal Transduction SystemsSignalingSpecimenStandardizationStatistical Data AnalysesStatistical Data AnalysisStatistical Data InterpretationStructure of respiratory epitheliumSupplementationSurfactant Protein ATLR proteinTOLLIPTOLLIP geneTestingTissuesToll-Interacting ProteinToll-Like Receptor Family GeneToll-like receptorsTranscriptionType A InfluenzaViralViral DiseasesVirus DiseasesWorkWuhan coronavirusairway epitheliumangiotensin converting enzyme 2angiotensin converting enzyme IIasthma attackasthma exacerbationasthmaticatopic triadatopyattenuateattenuatesbio-markersbiobankbiologicbiologic markerbiological signal transductionbiomarkerbiorepositoryclinical phenotypecoronavirus disease 2019 infectioncoronavirus disease 2019 viruscoronavirus disease-19 viruscost effectivecytokinedata interpretationdata managementexacerbation in asthmaexacerbation prone asthmaexacerbation prone asthmaticexperienceexperimentexperimental researchexperimental studyexperimentsfluidhCoV19host responsehuman diseasehuman subjectimmune modulatorsimmune system responseimmunologic substanceimmunological substanceimmunomodulatory moleculesimmunoregulatorimmunoregulatory moleculesimmunoresponseinfected with COVID-19infected with COVID19infected with SARS-CoV-2infected with SARS-CoV2infected with coronavirus disease 2019infected with severe acute respiratory syndrome coronavirus 2inflammatory modulationinfluenzavirusinterferon beta 2liquidmodel of animalnCoV2novelparticipant recruitmentpatient safetyphosphatidyl glycerolprogramsreceptorreceptor bindingreceptor boundrecruitrespiratory tract epitheliumsample collectionscreeningscreeningsspecimen collectionstatistical analysissurfactantsynergismviral infectionvirus infectionvirus-induced disease
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Full Description

The overall goal of this Asthma and Allergic Diseases Cooperative Research Center (AADCRC) proposal is to
elucidate the mechanisms by which the innate immune system affords protection against viral-induced

exacerbations in asthma. In the renewal of our AADCRC program, we will continue to focus on the critical

and often understudied innate immune factors the anion lipids of surfactant, (palmitoyl-oleoyl-

phosphatidylglycerol (POPG) and phosphatidylinositol (PI)) and Toll interacting protein (Tollip) and

surfactant protein-A (SP-A). Three inter-related projects are proposed in this application; the program will

employ use of biologic airway and peripheral systemic specimen samples obtained from well-phenotyped

participants with and without type 2 asthma and atopy through Core B, the Clinical Core. We hypothesize that

POPG/PI, Tollip and SP-A function as unique immune modulators which attenuate the effects of viral

infections in type 2 asthma, specifically RV-C, influenza A and SARS-CoV-2. Supplementation of

functional POPG/PI, SP-A and the IL-33 decoy receptor sST2 offer novel alternatives to reduce

exacerbations due to viral infections in asthma. Use of human samples is critical as animal models of SARS-

CoV-2, influenza and RVC are limited, and translational of findings to human disease can be variable. Therefore,

the goal of the Clinical Core is to provide services for our AADCRC investigators to perform safe, consistent

procedures in research participants for phenotyping and standardized, high quality collection of biologic airway

and peripheral systemic specimens, cost effective sample processing and data collection, with robust data

management and statistical analysis to test the hypotheses presented in each project. This Clinical Core will

extensively phenotype 100 participants comprised of 60 asthma (30 mild, and 30 severe) patients and 40 controls

(25 atopic, 15 non-atopic) for lung function testing, type 2 phenotyping, genotyping, nasal sampling, and to

participate in the bronchoscopy studies to understand the effectiveness of these innate immune modulators in

asthma and atopy, and in mild and severe asthma. The Clinical Core will coordinate and perform bronchoscopy

with bronchoalveolar lavage, nasal and epithelial cell brushings, and endobronchial biopsy on all participants.

The Clinical Core will be responsible for processing, storing, and distributing all samples collected from

participants, to each of the three projects. In this capacity, the Core will allow each clinical sample to be utilized

to its full potential and serve all projects equally. For all of the studies within the AADCRC utilizing human subject

samples, the Clinical Core will also be responsible for assuring patient safety, data confidentiality and full

regulatory compliance. A Biostatistics Unit is embedded in this core to integrate the clinical data with the

molecular/biomarker data to effectively model relationships between cellular features and clinical phenotypes in

asthma.

Grant Number: 5U19AI125357-10
NIH Institute/Center: NIH

Principal Investigator: Tara Carr

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