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Optimization of chimaeric HIV-1 virus-like particle (VLP) production and immunogenicity testing of VLPs in mice

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Bibliographic Details
Main Author: Pillay, Sirika
Other Authors: Rybicki, Ed
Format: Thesis
Language:English
Published: Department of Molecular and Cell Biology 2014
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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