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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/17292
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DC FieldValueLanguage
dc.contributor.advisorStampfli, M. R.-
dc.contributor.authorGaschler, Gordon J.-
dc.date.accessioned2015-05-13T14:56:46Z-
dc.date.available2015-05-13T14:56:46Z-
dc.date.issued2009-06-
dc.identifier.urihttp://hdl.handle.net/11375/17292-
dc.description.abstract<p> The cellular, molecular, and genetic mechanisms underlying the pathogenesis of Chronic Obstructive Pulmonary Disease (COPD) are not well understood. The purpose of this thesis was to address the hypothesis that microbial infection is important for the development and/or progression of COPD through investigation of how cigarette smoke alters the response to a bacterial challenge in a mouse model of cigarette smoke-exposure. To this end, in chapter 2 of this thesis we tested the hypothesis that cigarette smoke-exposure attenuates the ability of alveolar macrophages to sense microbial antigens through innate pattern recognition receptors. The central point of this study was the observation that alveolar macrophages isolated from cigarette smoke-exposed mice had attenuated expression of typical inflammatory cytokines following microbial stimulation. Building on this main observation, in chapter 3 we questioned what the consequences of this would be to an in vivo bacterial challenge with nontypeable Haemophilus influenzae. We demonstrated that cigarette smoke-exposure resulted in chronic inflammation, this inflammation was exacerbated following bacterial challenge, and perhaps most importantly, the nature of the inflammatory response was altered. Interestingly, an observation from the study in chapter 3 indicated that exacerbated inflammation in cigarette smoke-exposed mice may be beneficial for clearance of the bacteria, but may come at the expense of damage to the lungs. Consequently, in chapter 4 we questioned the strain and dose/ frequency stringencies of cigarette smoke-exposure on the observation of accelerated bacterial clearance. We demonstrated a role for antibodies in bacterial clearance. Collectively, this thesis provides insight into our understanding of COPD by demonstrating that cigarette smoke-exposure alters the pulmonary immune/ inflammatory response to a microbial challenge, which has a detrimental impact on the lungs. </p>en_US
dc.language.isoenen_US
dc.subjectcellularen_US
dc.subjectmolecularen_US
dc.subjectgenetic mechanismsen_US
dc.subjectpathogenesisen_US
dc.subjectChronic Obstructive Pulmonary Diseaseen_US
dc.subjectCOPDen_US
dc.subjectmicrobial infectionen_US
dc.subjectcigaretteen_US
dc.subjectsmokeen_US
dc.subjectexposureen_US
dc.subjectalveolar macrophagesen_US
dc.subjectantigensen_US
dc.subjectcytokinesen_US
dc.titleThe Impact Of Cigarette Smoke Exposure On Pathways of Microbial-Induced Pulmonary Inflammationen_US
dc.title.alternativeImpact Of Smoke On Microbial-Induced Pulmonary Inflammationen_US
dc.typeThesisen_US
dc.contributor.departmentMedical Sciencesen_US
dc.description.degreetypeThesisen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
Appears in Collections:Open Access Dissertations and Theses

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