grant

Sample Processing and Immunoassay Research Core

Organization JOHNS HOPKINS UNIVERSITYLocation BALTIMORE, UNITED STATESPosted 9 Sept 2016Deadline 31 Jul 2027
NIHUS FederalResearch GrantFY202519S Gamma GlobulinACE2Applications GrantsAssayAutoantibodiesAutoimmune StatusAutoimmunityBar CodesBase SequenceBioassayBiologicalBiological AssayBiopsyBlood PlasmaBlood SerumBudgetsCOVID crisisCOVID epidemicCOVID pandemicCOVID-19 crisisCOVID-19 epidemicCOVID-19 eraCOVID-19 global health crisisCOVID-19 global pandemicCOVID-19 health crisisCOVID-19 pandemicCOVID-19 periodCOVID-19 public health crisisCOVID-19 yearsCatalogingCell BodyCell IsolationCell SegregationCell SeparationCell Separation TechnologyCellsClinicalCollaborationsCollectionColorCommunitiesComplement ActivationComplexConsultationsCoupledCouplingCredentialingDNAData AnalysesData AnalysisDeoxyribonucleic AcidDepositDepositionDiagnosisDiseaseDisorderDistantELISAEndotheliumEnvironmentEnzyme-Linked Immunosorbent AssayFlow CytofluorometriesFlow CytofluorometryFlow CytometryFlow MicrofluorimetryFlow MicrofluorometryFundingGenerationsGenetic DiversityGenetic VariationGrant ProposalsHumanHuman BiologyIgMImmuneImmunesImmunoassayImmunoglobulin MImmunohistochemistryImmunohistochemistry Cell/TissueImmunohistochemistry Staining MethodImmunology procedureIn VitroInfrastructureInstitutionInvestigatorsKnowledgeLaboratoriesLeadershipMeasurementMetabolicModalityModern ManMolecularMonitorMusculoskeletal Pain DisorderNon-Polyadenylated RNANucleotide SequenceOrphan DiseasePBMCPathogenicityPathway interactionsPatientsPedigreePeer ReviewPeripheral Blood Mononuclear CellPhenotypePlasmaPlasma SerumPlayPopulationPreparationPreventionPriceProcessProductivityPublicationsQuality ControlRNARNA Gene ProductsRNA SeqRNA libraryRNA sequencingRNAseqRare DiseasesRare DisorderResearchResearch PersonnelResearch ResourcesResearch SpecimenResearchersResourcesReticuloendothelial System, Serum, PlasmaRetrievalRheumatic DiseasesRheumatismRheumatologic DiseasesRheumatologic DisorderRheumatologyRibonucleic AcidRoleRunningSARS-CoV-2 epidemicSARS-CoV-2 global health crisisSARS-CoV-2 global pandemicSARS-CoV-2 pandemicSARS-coronavirus-2 epidemicSARS-coronavirus-2 pandemicSamplingScholarshipScientific PublicationSerumServicesSevere Acute Respiratory Syndrome CoV 2 epidemicSevere Acute Respiratory Syndrome CoV 2 pandemicSevere acute respiratory syndrome coronavirus 2 epidemicSevere acute respiratory syndrome coronavirus 2 pandemicSiteSpecimenStandardizationStudy modelsSurvey InstrumentSurveysTemperatureTestingTimeTrainingValidationWhole BloodWorkangiotensin converting enzyme 2angiotensin converting enzyme IIautoimmune antibodyautoimmune rheumatic diseaseautoimmune rheumatologic diseaseautoreactive antibodybarcodebasebasesbiobankbiologicbiorepositorycareer developmentcell sortingclinical centerclinical phenotypecohortcomplement pathway regulationconsultationcoronavirus disease 2019 crisiscoronavirus disease 2019 epidemiccoronavirus disease 2019 global health crisiscoronavirus disease 2019 global pandemiccoronavirus disease 2019 health crisiscoronavirus disease 2019 pandemiccoronavirus disease 2019 public health crisiscoronavirus disease crisiscoronavirus disease epidemiccoronavirus disease pandemiccoronavirus disease-19 global pandemiccoronavirus disease-19 pandemicdata interpretationenzyme linked immunoassayexperienceflow cytophotometrygenetic pedigreehigh dimensionalityhuman diseaseimmunologic assayimmunologic assay/testinnovateinnovationinnovativeinterestlife-threatening COVIDlife-threatening COVID-19life-threatening SARS-CoV-2life-threatening coronavirus diseaselife-threatening coronavirus disease 2019life-threatening severe acute respiratory syndrome coronavirus 2membermouse modelmurine modelnucleic acid sequenceorphan disorderpathwaypatient subclasspatient subclusterpatient subgroupspatient subpopulationspatient subsetspatient subtypespedigree structurepreparationspricingprospectiverecruitself reactive antibodyserious COVIDserious COVID-19serious SARS-CoV-2serious coronavirus diseaseserious coronavirus disease 2019serious severe acute respiratory syndrome coronavirus 2severe COVIDsevere COVID-19severe COVID19severe SARS-CoV-2severe acute respiratory syndrome coronavirus 2 global health crisissevere acute respiratory syndrome coronavirus 2 global pandemicsevere coronavirus diseasesevere coronavirus disease 19severe coronavirus disease 2019severe severe acute respiratory syndrome coronavirus 2single cell analysissocial rolesynergismtooltranscriptome sequencingtranscriptomic sequencingvalidations
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Full Description

PROJECT SUMMARY
The Sample Processing and Immunoassay REsearch SPIRE Core (Core C) serves the

RDRCC research community as a centralized resource for preparation and storage of clinically

derived samples, for conducting a range of standard and innovative assays on clinically-derived

material, and for serving as a conduit to other relevant Institutional research Cores. Over decades,

this core has facilitated, through disease-specific Centers of Excellence, the generation of large

specimen bio-repositories obtained from well-pedigreed patient cohorts. This well-established Core,

by providing biospecimen acquisition, processing, storage, and retrieval services, has become a

critical partner in enabling discovery at the translational interface, and in attracting the interest of a

growing group of researchers from inside and outside the institution. In a survey of the research

community, this Core was viewed as a major resource, broadly enabling scholarship on well-defined

patient cohorts followed prospectively, with the storage of high-quality samples. The high-quality

assay services provided by Core C have resulted in numerous peer-reviewed publications, abstracts

and investigator-initiated grant proposals. The assay capabilities in the Core play a critical role in

pathway validation in human rheumatic disease cohorts. The aims of this proposal are to sustain,

grow and evolve this vital resource. We have added high-dimensional metabolic analysis of immune

cell populations by Dr. Jonathan Powell, and assays of immune effector function. Core leaders have

established interactions to guide investigators to the necessary institutional expertise and resources

that provide single cell analysis, sequence-based assays of immune activity, and advanced data

analysis and interpretation.

Core C will be directed by Drs. Casciola-Rosen and Darrah. Dr. Casciola-Rosen brings

decades of experience and rigor in running a highly effective and budget-stable research Core, and in

autoantibody discovery. Dr. Darrah recently assumed leadership of the Flow Core, and also brings

experience in sequence-based immune-based assays. Drs. Andrade and Gutierrez, both of whom

have many years of experience working with this Core team, will provide additional leadership. Dr.

Powell leads the high-dimensional immunometabolism analysis.

Grant Number: 5P30AR070254-10
NIH Institute/Center: NIH

Principal Investigator: LIVIA CASCIOLA-ROSEN

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