grant

Deconstructing the molecular and cellular mechanisms of psoriatic arthritis pain by an improved animal model

Organization DUKE UNIVERSITYLocation DURHAM, UNITED STATESPosted 1 Sept 2025Deadline 31 Aug 2028
NIHUS FederalResearch GrantFY2025Active OxygenAfferent NeuronsAnabolismAnalgesia TestsAnalgesic AgentsAnalgesic DrugsAnalgesic PreparationAnalgesicsAnimal ModelAnimal Models and Related StudiesAnodynesAntinociceptive AgentsAntinociceptive DrugsArthritisAttenuatedAutoimmuneBlocking AntibodiesBloodBlood PlasmaBlood Reticuloendothelial SystemBody TissuesCTLA-8CTLA-8 GeneCTLA8CTLA8 GeneCartilageCartilaginous TissueCell BodyCell Communication and SignalingCell SignalingCellsChondrocytesChronicClinicalCutaneousCutaneous DisorderCytotoxic T-Lymphocyte-Associated Antigen 8Cytotoxic T-Lymphocyte-Associated Antigen 8 GeneCytotoxic T-Lymphocyte-Associated Serine Esterase 8Cytotoxic T-Lymphocyte-Associated Serine Esterase 8 GeneD-MannoseDataDermatosesDevelopmentDorsal Root GangliaGeneticGoalsHospital AdmissionHospitalizationHumanIL-17IL-17 GeneIL-17AIL-17A GeneIL-23IL17IL17 ProteinIL17 geneIL17AIL17A GeneIP injectionIndividualInflammationInflammation MediatorsInflammatoryInjectionsInterleukin 17 (Cytotoxic T-Lymphocyte-Associated Serine Esterase 8)Interleukin 17 (Cytotoxic T-Lymphocyte-Associated Serine Esterase 8) GeneInterleukin 17 PrecursorInterleukin 17 Precursor GeneInterleukin-17InterleukinsInterventionIntracellular Communication and SignalingIntraperitoneal InjectionsIntrathecal InjectionsIon ChannelIonic ChannelsJAK kinaseJanus kinaseJointsKnock-outKnockoutLipidsLong-term painLysolecithinsLysophosphatidylcholinesMannanMannansMannopyranoseMannopyranosideMannoseMechanicsMediatingMediatorMedicalMembrane ChannelsMethodsMiceMice MammalsModelingModern ManMolecularMouse StrainsMovementMurineMusNociceptionNociception TestsOxygen RadicalsPainPain AssessmentPain MeasurementPain measurePainfulPathogenesisPatientsPersistent painPhenotypePhosphatidesPhospholipidsPilot ProjectsPlasmaPlasma SerumPolymersPre-Clinical ModelPreclinical ModelsPro-OxidantsProtocolProtocols documentationPsoriasisPsoriasis ArthropathicaPsoriatic ArthritisPublic HealthReactive Oxygen SpeciesRecurrent diseaseRelapsed DiseaseReportingReticuloendothelial System, Serum, PlasmaRoleSensory NeuronsSignal TransductionSignal Transduction SystemsSignalingSkinSkin DiseasesSkin Diseases and ManifestationsSolidSpinal GangliaTherapeuticTissuesTouchTouch sensationWild Type MouseWorkanimal painarthriticarthritic painarthritis painattenuateattenuatesbiological signal transductionbiosynthesisbody movementconstant paincutaneous diseasedermal diseasedermal disorderdevelopmentaldisabilitydorsal root ganglioneffectiveness validationimprovedinflammatory mediatorinsightinterleukin-23joint damagejoint degenerationjoint degradationjoint destructionjoint injuryjoint loadingjoint tissue degenerationjoint traumakeratinocytekinase inhibitorlasting painmechanicmechanicalmodel of animalmouse modelmurine modelnociceptivenovelon-going painongoing painpain assaypain behaviorpain killerpain medicationpain modelpain reliefpain relieverpainkillerpharmacologicpilot studypolymerpolymericpreventpreventingpsoriasiformpsoriaticrelieve painside effectskin disordersocial rolesuccesstactile sensationtherapeutic targettherapeutically effectivevalidate effectivenesswildtype mouse
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Description preview

Modified Project Summary/Abstract Section
Psoriasis (Ps) is an autoimmune-mediated systemic inflammatory skin disease. Approximately one-third of Ps

patients eventually develop psoriatic arthritis (PsA). PsA is one of the most common forms of arthritis, impacting

around 1 million individuals in the US. Mechanical pain associated with PsA in joints…

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