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Host Response and Pathogenesis in the Oral Cavity during SIV Infection

Host Response and Pathogenesis in the Oral Cavity during SIV Infection
SIV 感染期间口腔的宿主反应和发病机制
批准号:
7460897
负责人:
Michael D. George
金额:
$18.79万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-05 至 2010-06-30
关键词:
Acquired Immunodeficiency SyndromeAcuteAirAnimal ModelAnimalsAppearanceArchitectureArchivesBiologicalBiological AssayBiological MarkersBiomedical EngineeringBiometryBiotechnologyBloodBlood specimenCD4 Positive T LymphocytesCD8B1 geneCaliforniaCell SeparationCell physiologyCellsCheek structureChronicClinicalCollaborationsCytochrome P450DNA Microarray ChipDNA Microarray formatDataData AnalysesDeteriorationDifferentiation and GrowthDiseaseDisease ProgressionDisruptionDoctor of MedicineDoctor of PhilosophyDoctor of Veterinary MedicineDoseEnvironmentEnvironmental Risk FactorEpithelialEpithelial CellsEpitheliumEventExposure toFlow CytometryFormalinFunctional disorderFutureGene ExpressionGenesGenetic TranscriptionGrowthHIVHelper-Inducer T-LymphocyteHerpes zoster diseaseHistopathologyImmune responseImmunohistochemistryImmunologyImmunophenotypingImmunosuppressionInfectionInflammationInflammatoryInvestigationKnowledgeLasersLeadLinkLymphoid FollicleMacaca mulattaMediatingMessenger RNAMicroarray AnalysisMicrofabricationModelingMolecularMolecular ProfilingMorphologyMucinsNatural ImmunityNatureOligonucleotide MicroarraysOralOral ManifestationsOral cavityOral mucous membrane structureOrganismOropharyngealPathogenesisPathologyPatientsPatternPhysiologicalPolymerase Chain ReactionPredispositionProteinsRangeResearchResearch PersonnelRouteSIVSamplingSimian Acquired Immunodeficiency SyndromeSourceStagingStructureSuspension substanceSuspensionsSwabT-Cell DepletionT-Lymphocyte SubsetsTestingTherapeutic immunosuppressionTight JunctionsTimeTissue EmbeddingTissue SampleTissuesTongueUniversitiesViralViral Load resultVirusVirus DiseasesWorkantimicrobialbasebeta-Defensinsbeta-defensin-2cell growthdesigngene repressionimmune functionin vivoinnovationlaser capture microdissectionmicrobialmicroorganismoral biologypathogenpreventresponsesecondary infectionvirologyvirus host interactionvirus pathogenesis

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中文摘要
翻译
描述(由申请人提供):HIV感染患者进展为艾滋病的特征是出现机会性继发感染和免疫抑制,这些感染和免疫抑制是由于CD4+辅助T细胞功能的毁灭性丧失造成的。在直接接触病原体的隔室中,口腔粘膜特别容易受到影响,直接接触来自饮食和空气来源的微生物。口腔中的慢性继发性感染已知源于各种真菌、细菌、病毒和真核生物。合乎逻辑的是,组织形态和功能恶化的外在迹象是在当地环境的分子特征明显变化之前并由其驱动的,我们抗击艾滋病毒疾病进展的能力的改善取决于对这种转变的性质的理解。然而,口腔的发病机制、机会性继发感染的出现和发展为艾滋病之间的关系仍有待研究。建议的研究将阐明宿主与病毒相互作用的细节,并通过将功能基因表达谱的变化与疾病进展的不同表型相关性联系起来,增加我们对SIV感染所有阶段口腔致病机制和免疫学的了解。将采用创新的生物技术来分离上皮细胞和确定基因表达谱。对急性、慢性和艾滋病阶段感染的口腔生物学进行全面的临床和分子分析,将提供有关口腔免疫功能的前所未有的信息,识别SIV疾病进展的相关生物标志物,并为检验未来研究的假说奠定基础。
英文摘要
DESCRIPTION (provided by applicant): Progression to AIDS in HIV infected patients is characterized by the emergence of opportunistic secondary infections and immunosuppression that result from a devastating loss of CD4+ helper T cell function. Among the compartments with direct exposure to pathogens the oral mucosa is particularly susceptible, being directly exposed to microorganisms from dietary and air-borne sources. Chronic secondary infections in the oral cavity are known to originate from a variety of fungal, bacterial, viral, and eukaryotic organisms. It is logical that the outward signs of deterioration in tissue morphology and function are preceded and driven by distinct changes in the molecular profile of the local environment, and that improvements in our ability to combat HIV disease progression are dependent on understanding the nature of this transition. The relationship between pathogenesis of the oral cavity, the emergence of opportunistic secondary infections, and progression to AIDS, however, remains under-investigated. The studies proposed will elucidate details of host-virus interaction and increase our knowledge of pathogenic mechanisms and immunology in the oral cavity at all stages of SIV infection by linking changes in functional gene expression profiles with distinct phenotypic correlates of disease progression. Innovative biotechnologies for isolating epithelial cells and determining gene expression profiles will be employed. Comprehensive clinical and molecular analyses of oral biology in acute, chronic, and AIDS stage infections will provide unprecedented information about immune functions in the oral cavity, identify correlative biomarkers of SIV disease progression, and lay the ground work for developing hypotheses to test future studies.
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Risk and impact of infection resulting from treatment with chronic glucocorticoids in patients with rheumatoid arthritis
  • 批准号:
    10434713
  • 项目类别:
  • 资助金额:
    $17.46万
  • 财政年份:
    2018
  • 负责人:
    Michael D. George
  • 依托单位:
Risk and impact of infection resulting from treatment with chronic glucocorticoids in patients with rheumatoid arthritis
  • 批准号:
    10199930
  • 项目类别:
  • 资助金额:
    $17.46万
  • 财政年份:
    2018
  • 负责人:
    Michael D. George
  • 依托单位:
Role of host-microbe dysbiosis in enteropathy associated with SIV infection
  • 批准号:
    8467517
  • 项目类别:
  • 资助金额:
    $23.1万
  • 财政年份:
    2013
  • 负责人:
    Michael D. George
  • 依托单位:
Role of host-microbe dysbiosis in enteropathy associated with SIV infection
  • 批准号:
    8605513
  • 项目类别:
  • 资助金额:
    $19.25万
  • 财政年份:
    2013
  • 负责人:
    Michael D. George
  • 依托单位:
海外基金