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Role of innate immunity in HIV related vascular disease: biomarkers & mechanisms

Role of innate immunity in HIV related vascular disease: biomarkers & mechanisms
先天免疫在 HIV 相关血管疾病中的作用:生物标志物
批准号:
8927476
负责人:
Robert C Kaplan
金额:
$21.46万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-15 至 2015-08-31
关键词:
Acquired Immunodeficiency SyndromeAdultAnti-Retroviral AgentsAntigen PresentationApolipoproteinsArchivesArteriesAtherosclerosisAutomobile DrivingBenchmarkingBinding ProteinsBiological MarkersCD14 geneCD4 Positive T LymphocytesCardiovascular DiseasesCaringCarotid ArteriesCell CountChronicClinicalCoagulation ProcessCohort StudiesComorbidityComplement 4bDataDendritic CellsDevelopmentDisease ProgressionFCGR3B geneFlavoringGalectin 3Gene ExpressionGene Expression ProfileGenesGlucoseHIVHIV InfectionsHealthHepatitis C virusImmuneImmune systemInfectionInflammationInterventionInvestigationJointsKnowledgeLesionLinkLipidsMeasuresMediatingMessenger RNANatural ImmunityPPAR PathwayParticipantPathway interactionsPatientsPharmaceutical PreparationsPopulationRNARNA SequencesRecording of previous eventsResearchResearch Project GrantsRiskRisk FactorsRoleScanningSerumSignal PathwaySiteSmokingSpecimenStratificationSurfaceTestingThromboplastinThrombosisTranscriptUltrasonographyUnited States National Institutes of HealthUrsidae FamilyVascular DiseasesVascular remodelingVisitWomanarginasebasecardiovascular disorder preventioncardiovascular disorder riskchemokineclinical applicationclinically relevantco-infectioncohortcomplement C5bcytokinegenome wide association studygenome-wide analysishemoglobin-haptoglobin receptorhuman FRAP1 proteinimprovedinflammatory markerinsightintimal medial thickeningloss of functionmRNA Expressionmacrophagemonocytenovelprospectivepublic health relevancescavenger receptortranscriptome sequencing

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DESCRIPTION (provided by applicant): Innate immune system activation is a recognized feature of chronic HIV infection that may contribute to HIV disease progression as well increasingly important non-classic HIV complications such as cardiovascular disease (CVD). This proposal will a) identify mechanisms linking innate immunity with CVD in the setting of chronic, treated HIV infection; b) develop novel serum biomarkers for monocyte/macrophage related inflammation and coagulation that may stratify CVD risk in the HIV-infected population; c) use global sequencing of RNAs (RNA-Seq) to define HIV- and CVD-associated gain and/or loss of function of specific signaling pathways by studying CD14++ and CD14+CD16+ monocyte subsets from well-characterized HIV+ and HIV- patient groups. Extensively characterized HIV infected and HIV uninfected enrollees from the WIHS and MACS NIH cohorts are brought to bear in this interdisciplinary, multi-site investigation. This project will thereby provide insight into the observed links of HIV infection and related comorbidities (e.g., HCV coinfection) with CVD risk, identifying the innate immune system as a novel and modifiable explanatory pathway. This is of high clinical relevance given the need for improved CVD risk stratification, as well as the feasibility of intervening on mechanisms mediated by monocyte/macrophage activity.
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PASOS: Peripheral Artery Disease Study of SOL. An ancillary study of the Hispanic Community Health Study/Study of Latinos
Immunophenotyping for precision medicine for cardiovascular disease in people living with HIV
Immunophenotyping for precision medicine for cardiovascular disease in people living with HIV
Immunophenotyping for precision medicine for cardiovascular disease in people living with HIV
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