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Includes abstract.
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| Format: | Thesis |
| Language: | English |
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Department of Molecular and Cell Biology
2014
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| _version_ | 1867613206407544832 |
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| access_status_str | Open Access |
| author | Pillay, Sirika |
| author2 | Rybicki, Ed |
| author_browse | Pillay, Sirika Rybicki, Ed |
| author_facet | Rybicki, Ed Pillay, Sirika |
| author_sort | Pillay, Sirika |
| collection | Thesis |
| description | Includes abstract. |
| format | Thesis |
| id | oai:open.uct.ac.za:11427/4321 |
| institution | University of Cape Town (South Africa) |
| language | eng |
| last_indexed | 2026-06-10T12:32:27.580Z |
| license_str | Not specified — see source repository |
| provenance_str_mv | Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository |
| publishDate | 2014 |
| publishDateRange | 2014 |
| publishDateSort | 2014 |
| publisher | Department of Molecular and Cell Biology |
| publisherStr | Department of Molecular and Cell Biology |
| record_format | dspace |
| source_str | UCTD — University of Cape Town Open Access Repository |
| spelling | oai:open.uct.ac.za:11427/4321 Optimization of chimaeric HIV-1 virus-like particle (VLP) production and immunogenicity testing of VLPs in mice Pillay, Sirika Rybicki, Ed Meyers, Ann Cell Biology Includes abstract. Includes bibliographical references (leaves 139-148). The devastating effect the HIV pandemic has had on the human population in the last twenty five years has highlighted the great need to develop a prophylactic HIV vaccine. The manufacture of a vaccine has proven difficult though, with a number of successful designs in animal models having little success in humans. In view of this, there has been a need for novel vaccine approaches that are able to elicit effective cellular and humoral immune responses, both of which are believed to be important in the eradication of the virus. One such approach is the use of HIV-1 Gag VLPs as vaccine candidates. In this study, the production of two chimaeric (Gag VLP vaccine candidates (GagRT and GagTN) was optimized in insect cells, and their ability to enhance a murine immune response in a DNA prime-VLP boost vaccine strategy was evaluated. 2014-07-30T17:41:38Z 2014-07-30T17:41:38Z 2008 Master Thesis Masters MSc http://hdl.handle.net/11427/4321 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town |
| spellingShingle | Cell Biology Pillay, Sirika Optimization of chimaeric HIV-1 virus-like particle (VLP) production and immunogenicity testing of VLPs in mice |
| thesis_degree_str | Master's |
| title | Optimization of chimaeric HIV-1 virus-like particle (VLP) production and immunogenicity testing of VLPs in mice |
| title_full | Optimization of chimaeric HIV-1 virus-like particle (VLP) production and immunogenicity testing of VLPs in mice |
| title_fullStr | Optimization of chimaeric HIV-1 virus-like particle (VLP) production and immunogenicity testing of VLPs in mice |
| title_full_unstemmed | Optimization of chimaeric HIV-1 virus-like particle (VLP) production and immunogenicity testing of VLPs in mice |
| title_short | Optimization of chimaeric HIV-1 virus-like particle (VLP) production and immunogenicity testing of VLPs in mice |
| title_sort | optimization of chimaeric hiv 1 virus like particle vlp production and immunogenicity testing of vlps in mice |
| topic | Cell Biology |
| url | http://hdl.handle.net/11427/4321 |
| work_keys_str_mv | AT pillaysirika optimizationofchimaerichiv1viruslikeparticlevlpproductionandimmunogenicitytestingofvlpsinmice |