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Construction and evaluation of three candidate vaccines expressing HIV-1 subtype-C mosaic Gag

Includes bibliographical references

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Bibliographic Details
Main Author: Jongwe, Tsungai Ivai
Other Authors: Chapman, Ros
Format: Thesis
Language:English
Published: Division of Medical Biochemistry 2016
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access_status_str Open Access
author Jongwe, Tsungai Ivai
author2 Chapman, Ros
author_browse Chapman, Ros
Jongwe, Tsungai Ivai
author_facet Chapman, Ros
Jongwe, Tsungai Ivai
author_sort Jongwe, Tsungai Ivai
collection Thesis
description Includes bibliographical references
format Thesis
id oai:open.uct.ac.za:11427/17428
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:52:21.088Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2016
publishDateRange 2016
publishDateSort 2016
publisher Division of Medical Biochemistry
publisherStr Division of Medical Biochemistry
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/17428 Construction and evaluation of three candidate vaccines expressing HIV-1 subtype-C mosaic Gag Jongwe, Tsungai Ivai Chapman, Ros Williamson, Anna-Lise Douglass, Niki Chege, Gerald Medical Microbiology Includes bibliographical references Of the 35 million people living with HIV-1 globally, approximately 71.4% are in the resource-limited sub-Saharan Africa. The immense sequence diversity of HIV-1, even within subtypes, makes it challenging to develop effective vaccines that target a wide range of HIV subtypes. Mosaic immunogens have been computationally designed to specifically overcome this hurdle by maximizing the inclusion of common T cell epitopes. When compared to consensus immunogens, polyvalent mosaic immunogens of HIV-1 group M have shown increased breadth and depth of antigen-specific T-cell responses. More than 90% of HIV positive individuals in sub-Saharan Africa are infected with HIV-1 subtype C (HIV-1C). We therefore designed, constructed, and evaluated candidate vaccines expressing HIV-1C mosaic Gag (GagM) in a proof of concept study. Gag was chosen as the most appropriate target for a T cell-based vaccine as there are many studies correlating control of HIV viral load with T cell responses to Gag. The immunogen was designed by Fischer et al., 2007 (1). Three different vaccine platforms were chosen based on their different strengths to be used in prime-boost regimens to determine the immunogenicity of HIV-1C GagM in mice. The first was a pantothenic auxotroph of the tuberculosis vaccine Mycobacterium bovis Bacille Calmette Guérin (BCG). The second was a DNA vaccine vector with enhanced expression of transgenes due to a novel enhancer element from porcine circovirus type 1, which has been demonstrated to increase gene expression. The third vaccine vector selected was the well characterised poxvirus modified vaccinia Ankara (MVA). 2016-03-03T14:46:04Z 2016-03-03T14:46:04Z 2015 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/17428 eng application/pdf Division of Medical Biochemistry Faculty of Health Sciences University of Cape Town
spellingShingle Medical Microbiology
Jongwe, Tsungai Ivai
Construction and evaluation of three candidate vaccines expressing HIV-1 subtype-C mosaic Gag
thesis_degree_str Doctoral
title Construction and evaluation of three candidate vaccines expressing HIV-1 subtype-C mosaic Gag
title_full Construction and evaluation of three candidate vaccines expressing HIV-1 subtype-C mosaic Gag
title_fullStr Construction and evaluation of three candidate vaccines expressing HIV-1 subtype-C mosaic Gag
title_full_unstemmed Construction and evaluation of three candidate vaccines expressing HIV-1 subtype-C mosaic Gag
title_short Construction and evaluation of three candidate vaccines expressing HIV-1 subtype-C mosaic Gag
title_sort construction and evaluation of three candidate vaccines expressing hiv 1 subtype c mosaic gag
topic Medical Microbiology
url http://hdl.handle.net/11427/17428
work_keys_str_mv AT jongwetsungaiivai constructionandevaluationofthreecandidatevaccinesexpressinghiv1subtypecmosaicgag