Pneumonia is a leading cause of death worldwide, and can be caused by different types of pathogens, including viruses and bacteria. Influenza A virus is one of the most common viral causes of pneumonia, and seasonal strains infect 5-20% of the population of the United States each year. Seasonal strains are constantly evolving, and therefore vaccines must be updated and administered every year. Recent studies have indicated that influenza virus-specific CD4 T cells can provide protection during infection with strains of influenza A virus to which an individual does not have antibodies, thus understanding how these CD4 T cells respond to infection in the lungs is an important step towards more effective and enduring protection. My work provides insight into the specialized subsets present in the influenza A virus-specific CD4 T cell response in the lungs and demonstrates that this response is regulated by pulmonary antigen-presenting cells.
Group A Streptococcus is a bacterial cause of pneumonia with a 15-25% mortality rate, yet very little is known about the pulmonary CD4 or CD8 T cell responses to infection. My work maps the kinetics of and identifies requirements for CD4 and CD8 T cell accumulation in the lungs during pulmonary Group A Streptococcus infection.
Together, these studies contribute to our knowledge of how T cell responses are generated and regulated in response to pulmonary pathogens. These findings have the potential to inform development of novel treatment and prevention strategies.
| Identifer | oai:union.ndltd.org:uiowa.edu/oai:ir.uiowa.edu:etd-8092 |
| Date | 01 December 2014 |
| Creators | Hornick, Emma Elizabeth Lanning |
| Contributors | Legge, Kevin L. |
| Publisher | University of Iowa |
| Source Sets | University of Iowa |
| Language | English |
| Detected Language | English |
| Type | thesis |
| Format | application/pdf |
| Source | Theses and Dissertations |
| Rights | Copyright © 2014 Emma Elizabeth Lanning Hornick |
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