grant

Biomarkers Core (Core E)

Organization MASSACHUSETTS GENERAL HOSPITALLocation BOSTON, UNITED STATESPosted 15 Jul 2010Deadline 31 Dec 2026
NIHUS FederalResearch GrantFY2025(TNF)-α3-10CACT2AD dementiaAD pathologyAMCF-IAT744.1Act-2AgeAgingAlzheimer Type DementiaAlzheimer beta-ProteinAlzheimer disease dementiaAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's Amyloid beta-ProteinAlzheimer's DiseaseAlzheimer's amyloidAlzheimer's biomarkerAlzheimer's disease biological markerAlzheimer's disease pathologyAlzheimer's pathologyAlzheimers DementiaAlzheimer’s biological markerAlzheimer’s disease biomarkerAmyloidAmyloid Alzheimer's Dementia Amyloid ProteinAmyloid Beta-PeptideAmyloid Protein A4Amyloid SubstanceAmyloid beta-ProteinAmyloid βAmyloid β-PeptideAmyloid β-ProteinAssayAutomobile DrivingB cell differentiation factorB cell growth factorB cell stimulating factor 2B-Cell Differentiation FactorB-Cell Differentiation Factor-1B-Cell Differentiation Factor-2B-Cell Growth Factor-1B-Cell Growth Factor-IB-Cell Proliferating FactorB-Cell Stimulating FactorB-Cell Stimulating Factor-1B-Cell Stimulation Factor-1B-Cell Stimulatory Factor-1B-Cell Stimulatory Factor-2BCDFBCDF-1BCGFBCGF-1BCSF 1BSF-1BSF-2BSF1BSF2Beta Proprotein Interleukin 1BinetrakinBioassayBiologicalBiological AssayBiological MarkersBloodBlood BanksBlood PlasmaBlood Reticuloendothelial SystemBlood SerumBlood VesselsC1 qC1qCCL2CCL2 geneCCL4CCL4 geneCD106CD106 AntigensCXCL8CachectinCell LineCellLineCerebrospinal FluidChemokine (C-C Motif) Ligand 4Chemokine, CC Motif, Ligand 2Chemokine, CC Motif, Ligand 4ClinicalCo-StimulatorCognitionCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalCohort StudiesCollaborationsCollectionComplement 1qComplement C1qComplexConcurrent StudiesCostimulatorDNADataDeoxyribonucleic AcidDiagnosisDisturbance in cognitionDrugsDysfunctionELISAEnzyme-Linked Immunosorbent AssayEpidermal Thymocyte Activating FactorFIGF proteinFLK1FLT4 LigandFLT4-LFunctional disorderGCP1GrantHPGFHepatocyte-Stimulating FactorHistoryHybridoma Growth FactorIFN-GammaIFN-beta 2IFN-gIFN-γIFNB2IFNGIFNγIL-1 betaIL-1 βIL-1-bIL-1βIL-2IL-4IL-6IL-8IL1-BetaIL1-βIL1B ProteinIL1F2IL1βIL2 ProteinIL4 ProteinIL6 ProteinIL8IL8 geneINCAM-110Immune Activation 2Immune InterferonImmune responseImmunoassayImpaired cognitionIndividualInducible Cell Adhesion Molecule 110InflammationInflammatoryInjuryInterferon GammaInterferon Type IIInterleukin 1betaInterleukin 2Interleukin 2 PrecursorInterleukin IIInterleukin-1 betaInterleukin-1βInterleukin-2Interleukin-4Interleukin-4 PrecursorInterleukin-6Interleukine 2Interleukine 2 PrecursorInterleukine IIInvestigatorsK60KDR geneLaboratoriesLightLymphocyte Mitogenic FactorLymphocyte Stimulatory Factor 1MCAFMCGF-2MCP-1MCP1MGI-2MIP1BMIP1B1MMPsMT-bound tauMacrophage Inflammatory Protein 1-BetaMacrophage-Derived TNFMast Cell Growth Factor-2Matrix MetalloproteinasesMeasurementMeasuresMedicationMetabolicMethodsMicroRNAsMissionMitogenic FactorMolecularMonitorMonocyte Chemoattractant Protein-1Monocyte Chemotactic Protein-1Monocyte Chemotactic and Activating FactorMonocyte Chemotactic and Activating ProteinMonocyte Chemotactive and Activating FactorMonocyte Secretory Protein JEMonocyte-Derived TNFMyeloid Differentiation-Inducing ProteinNerve DegenerationNeurologyNeuron DegenerationNeurosciencesNon-Polyadenylated RNAP01 MechanismP01 ProgramPETPET ScanPET imagingPETSCANPETTPGF genePLGF-2ParticipantPharmaceutical PreparationsPhotoradiationPhysical activityPhysiopathologyPlGFPlGF proteinPlacental Growth FactorPlasmaPlasma SerumPlasmacytoma Growth FactorPositron Emission Tomography Medical ImagingPositron Emission Tomography ScanPositron-Emission TomographyPreinterleukin 1 BetaPreventative treatmentPreventionPreventive treatmentPrimary Senile Degenerative DementiaProceduresProcessProgram Project GrantProgram Research Project GrantsPsychiatryRNARNA Gene ProductsRad.-PETRecording of previous eventsResearchResearch PersonnelResearch Program ProjectsResearchersReticuloendothelial System, Serum, PlasmaRibonucleic AcidRoboticsSCYA2SCYA4SCYB8SamplingScientistSeasonsSerumSiteSmall Inducible Cytokine A2Small Inducible Cytokine A4SpecificityStrains Cell LinesSymptomsSynapsesSynapticT cell growth factorT-Cell Growth FactorT-Cell Growth Factor 2T-Cell Stimulating FactorTNFTNF ATNF AlphaTNF geneTNF-αTNFATNFαTSG-1TauopathiesTechnologyTestingThymocyte Stimulating FactorTimeTumor Necrosis FactorTumor Necrosis Factor-alphaVCAMVCAM-1VEGFVEGF ReceptorsVEGF-CVEGF-DVEGFRVEGFR-2VEGFR2VEGFsVPF ReceptorVascular Cell Adhesion MoleculeVascular Cell Adhesion Molecule-1Vascular Endothelial Cell Growth Factor ReceptorVascular Endothelial Growth Factor CVascular Endothelial Growth Factor DVascular Endothelial Growth Factor Receptor 2Vascular Endothelial Growth Factor Related ProteinVascular Endothelial Growth FactorsVascular Permeability Factor ReceptorWhole BloodWorka beta peptideabetaaged brainagesaging brainamyloid betaamyloid-b proteinb-ENAPbeta amyloid fibrilbio-markersbiobankbiologicbiologic markerbiomarkerbiomarker arraybiomarker panelbiorepositoryblood-based biomarkerblood-based markerbrain healthc-fos-induced growth factorcardiovascular riskcardiovascular risk factorcerebral spinal fluidcognitive dysfunctioncognitive losscohortcultured cell linedecline in functiondecline in functional statusdesigndesigningdrivingdrug/agentenzyme linked immunoassayexperiencefunctional declinefunctional status declinehistorieshost responseimmune system responseimmunoresponseinflammation markerinflammatory markerinjuriesinjury responseinjury to the vasculatureinterestinterferon beta 2lFN-Gammamarker panelmiRNAmicrotubule bound taumicrotubule-bound taunerve cell deathnerve cell lossneural degenerationneural imagingneuro-imagingneurodegenerationneurodegenerativeneurofilamentneuroimagingneurological degenerationneurological imagingneuron cell deathneuron cell lossneuron deathneuron lossneuronal cell deathneuronal cell lossneuronal deathneuronal degenerationneuronal lossneuropathologicneuropathologic tauneuropathologicalneuropathological tauneuropathologynew markernew technologynovel biomarkernovel markernovel technologiespathophysiologyplacenta growth factorpositron emission tomographic (PET) imagingpositron emission tomographic imagingpositron emitting tomographyprimary degenerative dementiaproduct placenta growth factorresponse to injuryresponse to therapyresponse to treatmentsenile dementia of the Alzheimer typesingle moleculesoluble amyloid precursor proteinspinal fluidsynapsetautau Proteinstau associated neurodegenerationtau associated neurodegenerative processtau driven neurodegenerationtau factortau induced degenerationtau induced neurodegenerationtau mediated neurodegenerationtau neurodegenerative diseasetau neuropathologytau pathologytau pathophysiologytau proteinopathytau related neurodegenerationtau-induced pathologytauopathic neurodegenerative disordertauopathytherapeutic responsetherapy responsetreatment responsetreatment responsivenessvascularvascular injuryτ Proteins
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Full Description

SUMMARY: CORE E- BIOMARKER CORE. The Biomarker Core supports the Harvard Aging Brain Study
(HABS) Program Project Grant (PPG) by processing and banking blood (plasma, serum, whole blood, buffy

coat, RNA, miRNA, DNA and cell lines) and cerebrospinal fluid (CSF) samples (Aim 1) collected by the Clinical

Core (Core B) from individuals (ages 50 to 94). Assays will be conducted on these biofluids to generate data

on amyloid-b ("A"), tau ("T") and neurodegeneration ("N") (Aim 2) and data on vascular injury and immune

response factors (Aim 3) for analysis by the Projects. The newly established Biomarker Core for HABS

includes over 1300 biofluid samples (blood and CSF) from 373 participants in Grant Cycles 1 and 2, and will

bank additional longitudinal samples over the next cycle. Bloods have been processed into plasma, serum,

whole blood, buffy coat, RNA, miRNA, DNA and cell lines, and CSFs are collected, processed and stored

according to best practices to minimize pre-analytical variability. ATN data has been generated using ultra-

sensitive single molecule array (Simoa) technology with assays for Ab42, NT1 tau and neurofilament-light (NfL)

in all samples to date as well as modifying factor data for vascular injury and immune response using

electrochemiluminescence ELISA. Samples have been distributed to collaborating scientists for additional

assays. Rigorous consideration of sample quality and assay sensitivity, specificity and precision have provided

confidence in the assays that will be used in the next cycle.

The Biomarker Core is comprised of a seasoned group of translational laboratory investigators with extensive

experience in molecular neurosciences and neuropathology, neurology, psychiatry, and biorepository

management. The Biomarker Core will work with the Clinical Core to continue optimal collection and on-site

processing procedures for blood and CSF, bank and distribute biofluids, and generate ATN and modifying

factor data using the most sensitive and reliable methods available. In order to bridge plasma with CSF and

better understand the potential of blood biomarkers of brain health, we will generate data in simultaneously

collected plasma and CSF in HABS and affiliated samples. Based on preliminary data and Project interests, in

the next Cycle, the Biomarker Core will measure Ab42, NT1 tau and NfL, vascular injury markers (especially

VEGF-related molecules) and Th1 and Th2 inflammatory markers (e.g., IFN-g and IL-4 respectively) and other

associated markers. It will also continue to identify, evaluate and implement novel technologies and biomarkers

for HABS. Data generated will be quality-controlled and transferred to DataCentral in coordination with the

Analytic Core for use in Projects 1-4.

Grant Number: 5P01AG036694-15
NIH Institute/Center: NIH

Principal Investigator: STEVEN ARNOLD

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