The progressive breakdown of cell mediated immunity is a feature in the pathology of HIV disease. Although not lost from the circulation, with disease progression cytotoxic T lymphocytes (CTL) are less able to contain numerous pathogens including HIV itself. Interleukin (IL)-7 and its signalling via the IL-7 receptor (CD127) is essential for optimal CTL activity. Our demonstration that fewer CD8+ T cells from HIV+ patients express CD127 as compared to healthy individuals, implicates a role for the regulation of CD127 expression in the immunopathogenesis of HIV. Thus, we hypothesize that altered CD127 expression and/or function on CD8+ T cells contributes to impaired cell mediated immunity.
This thesis reports an examination of which host or viral factors may be responsible for the down-regulation of CD127 on CD8+ T cells in HIV infection and the mechanism(s) by which these host and/or viral factors decrease CD127 expression on CD8+ T cells. It also assesses whether HIV down-regulates CD127 expression on CD8+ T cells in vitro, and evaluates if the functional capacity of CD127 is altered in HIV infection.
Of all the host and viral factors tested, IL-7, IL-4 and HIV-1tat caused a down-regulation in surface CD127 expression on CD8+ T cells, without affecting CD127 mRNA. IL-7 did not increase internalization of surface CD127, but caused shedding of the receptor. Furthermore, In vitro HIV infection of PBMC caused a down-regulation in surface CD127 expression on CD8+ T cells, without affecting CD127 mRNA, and seems to be caused by a soluble factor produced by the infected PBMCs. Finally, in response to IL-7, STAT5 phosphorylation in CD8+CD127 + cells from HIV+ individuals is significantly decreased compared to healthy controls. Proliferation of CD8+CD127 + cells in response to IL-7 is also significantly impaired. These data demonstrate a dysfunction in the IL-7 receptor system that may be explained by IL-7 specific signal transduction defects.
As the IL-7/IL-7R system and its disruption during HIV infection continue to be intensively studied, one will get a better understanding of HIV immunopathogenesis and the potential to lead to the development of novel immune based therapies will come about.
| Identifer | oai:union.ndltd.org:uottawa.ca/oai:ruor.uottawa.ca:10393/29833 |
| Date | January 2009 |
| Creators | Komsic-Vranjkovic, Agatha |
| Publisher | University of Ottawa (Canada) |
| Source Sets | Université d’Ottawa |
| Language | English |
| Detected Language | English |
| Type | Thesis |
| Format | 162 p. |
Page generated in 0.0021 seconds