Mechanisms of KSHV Transmission
Mechanisms of KSHV Transmission
批准号:
10398815
负责人:
BLOSSOM A DAMANIA
金额:
$58.37万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-05-01 至 2024-04-30
关键词:
Acquired Immunodeficiency SyndromeAffectAfrica South of the SaharaAntibodiesAreaB-LymphocytesBacteriaBiologicalBiological AssayBiologyButyratesCD19 geneCell LineChildhoodClinicalClinical ResearchClinical TrialsCohort StudiesCountryCytomegalovirusDNA copy numberDiseaseEncapsulatedEpidemicFutureGenesGenomeGoalsHerpesviridaeHerpesviridae InfectionsHumanHuman Herpesvirus 4Human Herpesvirus 8Human MilkImmuneIn VitroIndividualInfantInfectionInfectious AgentInnate Immune ResponseInterventionLifeLiquid substanceMapsMeasuresMethylationModelingMolecularMothersMucous MembraneNatural ImmunityOralOral cavityPatientsPersonsPhenotypePlaque AssayPlasmaPopulationResearch DesignRisk FactorsRouteSalivaSalivarySample SizeSamplingSeminal fluidSeroprevalencesSerumShapesSingle Nucleotide PolymorphismSpecimenStimulator of Interferon GenesSurfaceTestingTimeVaccine DesignVariantViralViral GenomeViral Load resultVirus DiseasesVolatile Fatty Acidsbasecohortepidemiology studyexperimental studyin vivoinfected B cellinfection riskkeratinocytelaboratory experimentmen who have sex with menmicrobiomemicrobiome signaturenoveloral microbiomeprospectivereactivation from latencyreproductivetransmission processtumorwhole genome
中文摘要
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英文摘要
Project Summary Abstract
Kaposi's Sarcoma-associated herpesvirus is transmitted primarily by saliva, though other routes
including semen and breastmilk have also been described. There exists a big discrepancy in KSHV
seroprevalence across different populations. It is less than 10% in the US, but > 50% in KSHV endemic
regions in Sub-Saharan Africa. Whereas the US AIDS-KS epidemic was driven by repeated contact
among MSM, in endemic regions KSHV is acquired in childhood. We are responding to RFA-CA-18-
013 to decipher how KSHV is transmitted. The overall goal of this application is to understand the
transmission of KSHV in molecular terms, with the ultimate goal being to inform vaccine design and
identify other means of disrupting transmission. To achieve this goal, we will investigate the three pillars
of transmissibility of infectious agents: (i) variance among KSHV strains using existing specimens from
large clinical cohorts, (ii) variance among the innate immune responses to KSHV infection, and (iii)
variance in the microbiome which may affect both KSHV itself (as measured by local viral load) and the
innate immune response to infection. In each case, we will start by profiling natural human variation
and then explore the function of significant viral and host variants in functional assays for entry,
replication and transmission.
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