Role of Reactive Oxygen Species in Nipah Virus Pathogenesis
Role of Reactive Oxygen Species in Nipah Virus Pathogenesis
批准号:
8911773
负责人:
Alexander Niclas Freiberg
金额:
$23.25万
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:
2014-08-13 至 2017-07-31
关键词:
Acute Lung InjuryAirAntioxidantsApicalBiologicalCCL2 geneCellsCommunicable DiseasesDataDevelopmentDiseaseDisease OutbreaksEncephalitisEotaxinEpithelial CellsFamilyFamily memberFoundationsGene ExpressionGenesGoalsHealthHenipavirusHenipavirus InfectionsHumanIL8 geneImmuneImmune responseImmune systemIn VitroInfectionInflammationInflammation MediatorsInflammatoryInterleukin-1Interleukin-6InterventionLeadLeukocytesLiquid substanceLungMediatingMediator of activation proteinMissionModelingMolecularNipah VirusOutcomeOxidative StressOxidative Stress PathwayParamyxoviridaePathogenesisPathogenicityPathway interactionsPlayProductionPublic HealthReactive Oxygen SpeciesRecruitment ActivityResearchResearch PersonnelRespiratory Syncytial Virus InfectionsRespiratory SystemRespiratory syncytial virusRespiratory tract structureRoleSignal TransductionSiteStructure of parenchyma of lungStructure of respiratory epitheliumSurfaceTestingTherapeutic InterventionTropismVirulenceVirusVirus DiseasesVirus ReplicationWorkcell typechemokinecytokineglobal healthimprovedin vivoin vivo Modelinflammatory lung diseaseinnovationlung xenograftmembermigrationmodel developmentmouse modelnovelnovel therapeutic interventionpreventreconstitutionrespiratoryresponsetransmission processvirus pathogenesis
中文摘要
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英文摘要
DESCRIPTION (provided by investigator): Here we seek to study the role of Reactive Oxygen Species (ROS) in Nipah virus (NiV)pathogenesis. The long-term goal to identify host genes and virulence determinants that will serve as targets for therapeutic intervention strategies to preven and treat lethal NiV infection. The objective here is to identify key mediators of NiV pathogenesis using novel and physiologically relevant in vitro and in vivo models of the human respiratory tract. Our central hypothesis is that NiV infection of human respiratory epithelium results in induction of ROS production, signaling key pro-inflammatory mediators and resulting in recruitment of immune cells. The rationale for the proposed research is that, once we confirm the role of ROS in henipavirus pathogenesis, we can use these targets for the development of novel therapeutic intervention strategies to treat and prevent lethal disease. We plan to test our central hypothesis by pursuing the following two specific aims: 1. Define the functional roles of ROS induction using our newly developed NiV infection model of primary human airway epithelial cells and 2. Validate the in vivo role of human respiratory epithelium in NiV-induced cellular recruitment by using a novel humanized mouse model. Under the first aim, we will confirm induction of ROS in primary human respiratory epithelial cells grown at an air-liquid interface, identify which key inflammatory mediators are important of transendothelial migration of immune cell and test whether treatment with antioxidants will result in a reduction of the levels of these cytokine/chemokines and recruitment of immune cells. Under the second aim we will determine what cells are recruited to the human lung following NiV infection using a novel humanized mouse model with human lung xenografts, confirm the induction of ROS in this model and test the effect of antioxidant treatment. The approach is innovative because it uses novel and biologically relevant models of the human respiratory tract to focus on the early steps in henipavirus pathogenesis. The proposed research is significant because the availability of these models to study henipavirus pathogenesis is expected to lead to the identification of host and virus factors critical for the lethal outcome following human henipavirus infection.
期刊论文(4)
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科研奖励(0)
会议论文
Ebola virus infection of the female reproductive system
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批准号:10396086
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项目类别:
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资助金额:$23.7万
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财政年份:2021
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负责人:Alexander Niclas Freiberg
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依托单位:
Therapeutic efficacy of favipiravir against henipavirus infections
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项目类别:
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财政年份:2021
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依托单位:
Ebola virus infection of the female reproductive system
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批准号:10196662
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项目类别:
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资助金额:$19.75万
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财政年份:2021
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依托单位:
Bioavailable proteasome inhibitors as broad-spectrum antivirals
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项目类别:
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资助金额:$41.59万
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财政年份:2012
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依托单位:
Bioavailable proteasome inhibitors as broad-spectrum antivirals
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项目类别:
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资助金额:$12.57万
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财政年份:2012
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负责人:Alexander Niclas Freiberg
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依托单位:
Bioavailable proteasome inhibitors as broad-spectrum antivirals
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批准号:8391397
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项目类别:
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资助金额:$23.4万
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财政年份:2012
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负责人:Alexander Niclas Freiberg
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依托单位:
国内基金
海外基金
湍流和化学交互作用对H2-Air-H2O微混燃烧中NO生成的影响研究
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批准号:51976048
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项目类别:面上项目
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资助金额:61.0万元
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批准年份:2019
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负责人:邱朋华
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依托单位: