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Title: Characterisation of the acute inflammation during murine pneumococcal pneumonia
Author: Kerr, Alison Russell
ISNI:       0000 0001 3597 5981
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 2000
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We have established a murine model of pneumococcal pneumonia in order to characterise the host inflammatory response. Intranasal infection with Streptococcus pneumoniae resulted in constant bacterial loads within airways of susceptible mouse strains whilst the pathogen burden increased in both the lung tissues and bloodstream. The bacteria induced inflammation that was evident as perivascular cell recruitment in histological sections. Mast cell granule staining indicated that this population degranulated early in the inflammatory response, releasing TNFa into the lung environment. Levels of TNFa and IL-1b increased during mid infection with release of IL-6 and the anti-inflammatory cytokine IL-10 not occurring until late infection. Kinetics of IL-10 were too slow to prevent inflammation causing damage to the host tissues. The total protein levels in bronchoalveolar lavage fluid (a marker of the integrity of the alveolar/capillary barrier) increased significantly during the experiment. Dose response results indicate that there is likely to be a threshold number of bacteria required to induce this inflammatory response both in the lungs and bloodstream. Inoculation of bacteria into a mouse strain resistant to the above infection resulted in bacterial clearance from both the pulmonary airways and tissues, with few more becoming bacteraemic. The location and timing of the inflammatory response in this mouse strain was significantly different. Inflammatory cell influx occurred mainly within the airways, with perivascular areas unaffected. Mast cell degranulation occurred rapidly following infection. TNF activity and IL-1b levels within lung airways were induced earlier and to a greater extent than in susceptible mice. IN contrast, the levels of TNF activity and IL-6 within lung tissues were lower in resistant mice. Although damage to lung integrity still occurred, this was only transient and evident during early/mid infection.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: QR180 Immunology