Pulmonary Pathogen-Recognition Pathways in Melioidosis
Pulmonary Pathogen-Recognition Pathways in Melioidosis
批准号:
7571767
负责人:
Timothy Eoin West
金额:
$12.74万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-12-01 至 2013-11-30
关键词:
Adaptor Signaling ProteinAddressAdvisory CommitteesAerosolsAlveolar MacrophagesAntibiotic TherapyAntibody FormationBacteriaBacterial InfectionsBacterial PneumoniaBiologyBlocking AntibodiesBone MarrowBreathingBurkholderia pseudomalleiCaspase-1CategoriesCause of DeathCell DeathCellsCenters for Disease Control and Prevention (U.S.)CollaborationsCommunicable DiseasesComplexCytochalasin DDendritic CellsDendritic cell activationDevelopmentDevelopment PlansDiseaseDisease modelDoseEducational CurriculumEnvironmentEnzymesEpithelial CellsFlagellinGenesGoalsHealthHistopathologyHost DefenseHost Defense MechanismHost resistanceImmuneImmune responseImmunityImmunoglobulin GImmunoglobulin MImmunologistImmunologyIn Situ Nick-End LabelingIn VitroIndividualInfectionInflammatory ResponseInstructionInterleukin-1Interleukin-1 ReceptorsInterleukin-18InvestigationKnockout MiceKnowledgeLaboratoriesLeadLigandsLipopolysaccharidesLungMastigophoraMeasuresMediatingMelioidosisMentorshipMethodsMissionModelingMorbidity - disease rateMultiprotein ComplexesMusNatural ImmunityNatural Killer CellsNuclearNuclear TranslocationPathologistPathway interactionsPhenotypePneumoniaPopulationPrincipal InvestigatorProcessProductionPublic HealthReceptor SignalingResearchResearch PersonnelResourcesRespiratory Tract InfectionsRoleScientistSepsisSerumSignal PathwaySignal TransductionSplenocyteTLR2 geneTLR4 geneTLR5 geneTdT-Mediated dUTP Nick End Labeling AssayTestingToll-like receptorsTrainingUnited States National Institutes of HealthUniversitiesWashingtonWestern Blottingaerosolizedbacterial geneticsburden of illnesscareercareer developmentcytokinecytosolic receptorcytotoxicitydisabilityinterleukin-18 receptorlaboratory facilitymacrophagemortalitymultidisciplinarynovel therapeuticspathogenprogramsreceptorresponsesensorskillssymposiumtranslational studyuptake
中文摘要
描述(由申请人提供):韦斯特博士的职业目标是成为一名精通肺宿主防御机制转化研究的物理学家,专注于细菌性呼吸道感染,这是全球发病率和死亡率的主要原因。这份职业发展申请描述了一个有两个主要目标的综合课程。第一个目标是为候选人提供深入的肺生物学和免疫学知识,并扩大实验室方法的培训,以促进他的职业发展走向独立。第二个目标是确定类鼻疽病的肺部病原体识别途径,类鼻疽病是一种致命的热带感染,由假伯克氏菌引起,是一种潜在的气溶胶生物武器。韦斯特博士的职业发展计划包括教学课程、参加科学研讨会和会议、实践实验室技能的指导、与华盛顿大学和国外多学科科学家小组的密切合作、一位有成就的高级研究员的密集指导以及学术咨询委员会的监督。该研究计划结合了各种基因敲除小鼠,各种原代细胞的体外研究,空气传播疾病的复杂小鼠模型,以及使用专门的实验室设施。本提案的具体目的是:1)鉴定toll样受体(TLRs) -跨膜病原体识别传感器-和介导假假芽孢杆菌体外识别的下游信号通路;2)确定TLR信号通路在肺炎类鼻疽病中影响先天免疫和适应性免疫的特定成分;3)确定胞质ice -蛋白酶激活因子(IPAF)/caspase-1信号轴在类melidosis中的相关作用。在进行这些研究时,West博士将在Shawn Skerrett博士的密切监督下进行,Shawn Skerrett博士是一位杰出的研究者,他的研究重点是利用小鼠疾病模型研究细菌性肺炎的先天免疫。韦斯特博士还将与一个由微生物学家、免疫学家和病理学家组成的优秀团队合作,他们在宿主-病原体相互作用、宿主和细菌遗传学以及小鼠肺炎模型方面分享特定的专业知识。华盛顿大学的科学家拥有丰富的学术和物质资源,这为他们的职业发展培训创造了理想的环境。此外,华盛顿大学肺病、传染病和全球健康研究项目的综合优势将极大地促进韦斯特博士朝着他的职业目标前进。相关性(见说明):这项研究直接解决了NIH的既定使命,即追求减少疾病和残疾负担的基础科学知识。这些研究将增加我们对致命细菌感染类鼻疽的认识,这是一个日益严重的公共卫生问题,并可能最终导致这种疾病的新治疗方法的发展。这些发现也可能适用于其他呼吸道感染——世界范围内导致死亡和残疾的主要原因,对穷人的影响尤为严重。
英文摘要
DESCRIPTION (provided by applicant): Dr. West's career goal is to become a physican-scientist proficient in the translational study of mechanisms of pulmonary host defense, with a focus on bacterial respiratory infections, major causes of morbidity and mortality around the world. This career development application describes an integrated curriculum with two main objectives. The first objective is to provide the candidate with an in-depth knowledge of lung biology and immunology, and expanded training in laboratory methods to facilitate his career development toward independence. The second objective is to define pulmonary pathogen-recognition pathways in melioidosis, a lethal tropical infection caused by Burkholderia pseudomallei, a potential aerosol bioweapon. Dr. West's career development plan comprises didactic coursework, participation in scientific seminars and conferences, instruction in practical laboratory skills, close collaborations with a multidisciplinary group of scientists at University of Washington and abroad, intensive mentorship by an accomplished senior investigator, and oversight by an academic advisory committee. The research plan combines a wide assortment of gene knockout mice, in vitro studies of a variety of primary cells, sophisticated murine models of airborne disease, and access to specialized laboratory facilities. The specific aims of this proposal are: 1) to identify Toll-like receptors (TLRs) - transmembrane pathogen-recognition sensors - and downstream signaling pathways that mediate recognition of B. pseudomallei in vitro; 2) to define TLR signaling pathways in pneumonic melioidosis that influence specific components of innate and adaptive immunity; and 3) to determine the related role of the cytosolic ICE-protease-activating factor (IPAF)/caspase-1 signaling axis in melioidosis. In performing these studies, Dr. West will be closely supervised by Dr. Shawn Skerrett, a distinguished investigator whose research focus is the investigation of innate immunity in bacterial pneumonias using murine models of disease. Dr. West will also collaborate with an outstanding team of microbiologists, immunologists, and pathologists who share specific expertise in host-pathogen interactions, host and bacterial genetics, and mouse pneumonia models. The extensive academic and physical resources available to University of Washington scientists create an ideal environment for this career development training. Furthermore, the combined strengths of University of Washington's pulmonary, infectious diseases, and global health research programs will greatly facilitate Dr. West's progression toward his career goal. RELEVANCE (See instructions): This research directly addresses the stated mission of the NIH to pursue fundamental scientific knowledge that reduces the burden of illness and disability. These studies will increase our understanding of the lethal bacterial infection melioidosis, a growing public health problem, and may ultimately lead to the development of new treatments for this disease. The findings may also be applicable to other respiratory infections - leading causes of death and disability worldwide that disproportionately impact the poor.
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会议论文
Cellular GWAS of the host-pathogen interaction in melioidosis
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批准号:9371825
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项目类别:
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资助金额:$23.24万
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财政年份:2017
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负责人:Timothy Eoin West
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依托单位:
Regulation of host inflammatory responses and outcome in melioidosis by TLR5
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批准号:8273969
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项目类别:
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资助金额:$58.07万
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财政年份:2012
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负责人:Timothy Eoin West
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依托单位:
Regulation of host inflammatory responses and outcome in melioidosis by TLR5
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批准号:8843030
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项目类别:
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资助金额:$47.26万
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财政年份:2012
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负责人:Timothy Eoin West
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依托单位:
Regulation of host inflammatory responses and outcome in melioidosis by TLR5
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批准号:9057608
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项目类别:
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资助金额:$32.1万
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财政年份:2012
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负责人:Timothy Eoin West
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依托单位:
Regulation of host inflammatory responses and outcome in melioidosis by TLR5
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批准号:8661279
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项目类别:
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资助金额:$63.57万
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财政年份:2012
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负责人:Timothy Eoin West
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依托单位:
Regulation of host inflammatory responses and outcome in melioidosis by TLR5
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批准号:8469901
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项目类别:
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资助金额:$57.36万
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财政年份:2012
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负责人:Timothy Eoin West
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依托单位:
Pulmonary Pathogen-Recognition Pathways in Melioidosis
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批准号:8197455
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项目类别:
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资助金额:$12.74万
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财政年份:2008
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负责人:Timothy Eoin West
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依托单位:
Pulmonary Pathogen-Recognition Pathways in Melioidosis
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批准号:8014917
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项目类别:
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资助金额:$12.74万
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财政年份:2008
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负责人:Timothy Eoin West
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依托单位:
Pulmonary Pathogen-Recognition Pathways in Melioidosis
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批准号:8389612
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项目类别:
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资助金额:$12.74万
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财政年份:2008
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负责人:Timothy Eoin West
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依托单位:
Pulmonary Pathogen-Recognition Pathways in Melioidosis
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批准号:7743090
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项目类别:
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资助金额:$12.74万
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财政年份:2008
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负责人:Timothy Eoin West
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依托单位:
海外基金