grant

Cannabis, HIV and Mental Processing Systems (CHAMPS)

Organization WASHINGTON UNIVERSITYLocation SAINT LOUIS, UNITED STATESPosted 1 Aug 2021Deadline 31 May 2027
NIHUS FederalResearch GrantFY20259-ene-TetrahydrocannabinolAIDS VirusAcquired Immune Deficiency Syndrome VirusAcquired Immunodeficiency Syndrome VirusAffectAmmon HornBlood PlasmaBlood monocyteBrainBrain InflammationBrain Nervous SystemCCL2CCL2 geneCD14CD14 geneCD8CD8 CellCD8 T cellsCD8 lymphocyteCD8+ T cellCD8+ T-LymphocyteCD8-Positive LymphocytesCD8-Positive T-LymphocytesCD8BCD8B1CD8B1 geneCannabidiolCannabisCellular Immune FunctionCellularityChemokine, CC Motif, Ligand 2ClassificationCognitionCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalComplexCornu AmmonisCorticospinal TractsCounselingCross Sectional AnalysisCross-Sectional AnalysesCross-Sectional StudiesCross-Sectional SurveyD9-tetrahydrocannabinolDataDelta-9-TetrahydrocannabinolDisease Frequency SurveysDisturbance in cognitionDrugsEmploymentEncephalitisEncephalonExhibitsExposure toGeneral PopulationGeneral PublicHIVHIV InfectionsHTLV-III InfectionsHTLV-III-LAV InfectionsHealthHippocampusHuman Immunodeficiency VirusesHuman T-Lymphotropic Virus Type III InfectionsImmediate MemoryImmuneImmune Cell ActivationImmune MarkersImmunesImmunologic MarkersImpaired cognitionInflammationLAV-HTLV-IIILYT3LearningLegalLifeLymphadenopathy-Associated VirusMCAFMCP-1MCP1MacrophageMarrow monocyteMeasurementMeasuresMedical MarijuanaMedicationMedicinal MarijuanaMedicineMemoryMethodologyMethodsModelingMonocyte Chemoattractant Protein-1Monocyte Chemotactic Protein-1Monocyte Chemotactic and Activating FactorMonocyte Chemotactic and Activating ProteinMonocyte Chemotactive and Activating FactorMonocyte Secretory Protein JENeopterinNeuropsychologiesNeuropsychologyOutcomeParietal LobePerforant PathPerforant PathwayPerforating FasciculusPerformancePeripheralPersonsPharmaceutical PreparationsPhenotypePlasmaPlasma SerumPrevalencePrevention GuidelinesPsyche structureQualifyingRecreational DrugsReportingResearch DesignReticuloendothelial System, Serum, PlasmaSCYA2SamplingScienceShort-Term MemorySmall Inducible Cytokine A2StructureStudy TypeSurvival RateSystemSystematicsT8 CellsT8 LymphocytesTHC co-useTHC concentrationTHC useTemporal LobeTestingTetrahydrocannabinolTetrahydrocannabinol co-useTetrahydrocannabinol useUrineViralVirus-HIVantiretroviral therapyantiretroviral treatmentcannabis usecannabis usercognitive dysfunctioncognitive losscognitive performancedata-driven modeldelta(1)-THCdelta(1)-Tetrahydrocannabinoldelta(9)-THCdelta(9)-Tetrahydrocannabinoldrug/agentexecutive controlexecutive functionhigh dimensionalityhippocampalimmune activationimmune functionimmune healthimmune system healthimmune-based biomarkersimmunological biomarkersimmunological markersimprovedindexinginsightmarijuana usemarijuana usermedical cannabismedicinal cannabismentalmonocyteneural imagingneuro-imagingneuroimagingneurological imagingneuropsychologicnovelparietal cortexphenotypic dataprogramsstudy designsubstance usesubstance usingtemporal cortextetrahydrocannabinol concentrationtherapeutic cannabistherapeutic marijuanatreatment guidelinesworking memoryΔ(1)-THCΔ(1)-tetrahydrocannabinolΔ(9)-THCΔ(9)-tetrahydrocannabinolΔ-9-tetrahydrocannabinolΔ9-tetrahydrocannabinol
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Full Description

ABSTRACT/PROJECT SUMMARY
This proposal employs novel methods to identify key determinants and consequences of concurrent HIV

infection and regular cannabis use. We will acquire extensive phenotype data from peripheral and brain

markers of immune activation, brain structure, and neuropsychological performance (NP) in persons living

with HIV (PLWH) receiving combination anti-retroviral therapy (cART) (80 regular cannabis users and 80

non-users) and HIV uninfected (HIV-) controls (80 regular cannabis users and 80 non-users). Our overall

hypothesis is that cannabis use leads to increases in inflammation in the peripheral and brain compartments.

We also hypothesize that phenotypic signatures due to regular cannabis use and HIV will be delineated through

NP and brain volumetrics. In Aim 1 we hypothesize that regular cannabis use will increase both peripheral and

brain immune indices in PLWH on cART. In Aim 2 we hypothesize that regular cannabis use will lead to a

worsening of NP and reductions in brain volumetrics in both PLWH on cART and HIV- controls. This proposal

will provide key insights into the effects of regular cannabis and HIV on peripheral and brain markers of

immune function and NP in PLWH and HIV- controls. These insights are critical for cure strategies and

ongoing HIV treatment initiatives.

Grant Number: 5R01DA054009-05
NIH Institute/Center: NIH

Principal Investigator: Beau Ances

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