Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/117794
Type: | Theses |
Title: | The Mucosal Barrier in Chronic Rhinosinusitis |
Author: | Murphy, Jae Viktor |
Issue Date: | 2018 |
School/Discipline: | Adelaide Medical School |
Abstract: | Chronic rhinosinusitis (CRS) is a heterogeneous disease characterised by inflammation of the nose and paranasal sinuses, which results in nasal obstruction, rhinorrhoea, post-nasal drip, facial pressure, and alterations in smell. The pathophysiology of CRS is complex and involved interactions between the host, microbial flora, and environment. Studies have shown that the mucosa of CRS sufferers demonstrates signs of defective barrier function, although little is known about the contributing factors to this process. Understanding epithelial barrier dysfunction in the gastrointestinal, skin, and pulmonary systems highlights the various contributing factors to this process, which may be paralleled in the paranasal sinuses. It appears that bacterial mediated mechanism, inflammatory surroundings, and the divalent metal zinc are important in these systems. Staphylococcus aureus has been implicated in the pathogenesis and persistence of CRS, poorer wound healing, and increased disease severity. Additionally, it is known that S. aureus secretes an unknown factor that perturbs the airway barrier in-vitro. Previous research has suggested that zinc concentrations may be lower in CRS, particularly in patients with nasal polyposis, however little is known about the consequences of localised zinc deficiency in CRS. This thesis examines the S. aureus secretome to elucidate the factor or factors involved in barrier disruption. Furthermore, the role of zinc in mucosal barrier integrity and CRS has been delineated. |
Advisor: | Wormald, Peter-John Psaltis, Alkiviadis Vreugde, Sarah |
Dissertation Note: | Thesis (Ph.D.) -- University of Adelaide, Adelaide Medical School, 2018 |
Keywords: | Chronic rhinosinusitis tight junction barrier Staphylococcus aureus zinc |
Provenance: | This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals |
Appears in Collections: | Research Theses |
Files in This Item:
File | Description | Size | Format | |
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Murphy2018_PhD.pdf | Thesis | 3.66 MB | Adobe PDF | View/Open |
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