HSV-1 and HIV-1 co-infection of human macrophages represents a clinically relevant model with which to investigate the host-pathogen interactions between macrophages and viruses. In this thesis, I demonstrate that HSV-1 productively infects human monocyte derived macrophages, with associated cell death and type I IFN responses, and additionally, that a proportion of macrophages support latent HSV-1 infection. I de ne latency as the absence of lytic gene transcription, virion production and cell death, in the presence of persistent expression of the HSV-1 latency associated transcript (LAT). I also demonstrate that HSV-1 super-infection increases HIV-1 transcription, and that latent HSV-1 can be reactivated by HIV-1. HSV-1 latent infection of neurons is well established, but this is the rst report, to my knowledge, of HSV-1 latent infection of myeloid lineage cells. The potential for macrophage reservoirs of latent HSV-1 may be an important factor for the clinical management of persistent reactive HSV-1 disease. Furthermore, HIV-1 infection in vivo is known to increase the frequency of HSV-1 reactivation in the host through the indirect mechanism of immune system suppression. However, a direct interaction between cells latently infected with HSV and HIV-1 has not previously been observed. Reactivation of latent HSV by HIV-1 therefore provides a novel mechanism for the well-established clinical synergy between these viruses.
| Identifer | oai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:746668 |
| Date | January 2017 |
| Creators | Hughes, R. |
| Publisher | University College London (University of London) |
| Source Sets | Ethos UK |
| Detected Language | English |
| Type | Electronic Thesis or Dissertation |
| Source | http://discovery.ucl.ac.uk/1563691/ |
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