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Determination of the role of cytokines using gene deficient mice in African trypanosomiasis infection

Includes bibliographical references.

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Bibliographic Details
Main Author: Barkhuizen, Mark
Other Authors: Brombacher, Frank
Format: Thesis
Language:English
Published: Division of Immunology 2014
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access_status_str Open Access
author Barkhuizen, Mark
author2 Brombacher, Frank
author_browse Barkhuizen, Mark
Brombacher, Frank
author_facet Brombacher, Frank
Barkhuizen, Mark
author_sort Barkhuizen, Mark
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/3119
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:03.909Z
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 Division of Immunology
publisherStr Division of Immunology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/3119 Determination of the role of cytokines using gene deficient mice in African trypanosomiasis infection Barkhuizen, Mark Brombacher, Frank Magez, Sefan Immunology Includes bibliographical references. African trypanosomiasis encompasses diseases caused by pathogenic trypanosomes, infecting both humans and animals alike. To determine the immunological role of IL=12 family members in Trypanosoma brucei brucei, Trypanosoma evansi and Trypanosoma congolense infections, IL-12p35¯/¯, IL-12p40¯/¯ and IL-12p35¯/¯/p40¯/¯ mice were used. While the two latter mouse strains lack all IL-12 homologues, IL-12p35¯/¯ mice still produce IL-12p80 homodimers and IL-23. In infection with T.b. brucei and T.evansi; IL-12p35¯/¯, IL-12p40¯/¯ or IL-12p35¯/¯/p40¯/¯ mice were susceptible to both these pathogens, demonstrated by increased mortality compared to wild type C57BL/6 mice. The different IL-12 deficient mouse strains showed similar mortality kinetics, suggesting that IL-12p70 but not the IL-12p80 homodimer or IL-23 plays a crucial role in survival. Similarly, parasitemia control was reduced in the absence of IL-12p70. While plasma levels of IgM and IgG2c were similar between IL-12 deficient mice and wild type mice, IF-γ production. As IFN-γR¯/¯ mice were also highly susceptible to both T.b. brucei and T. evansi, IL-12p70-dependent IFN-γ production seems to be important mechanism involved in resistance against both these pathogens. 2014-07-28T14:54:13Z 2014-07-28T14:54:13Z 2008 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/3119 eng application/pdf Division of Immunology Faculty of Health Sciences University of Cape Town
spellingShingle Immunology
Barkhuizen, Mark
Determination of the role of cytokines using gene deficient mice in African trypanosomiasis infection
thesis_degree_str Doctoral
title Determination of the role of cytokines using gene deficient mice in African trypanosomiasis infection
title_full Determination of the role of cytokines using gene deficient mice in African trypanosomiasis infection
title_fullStr Determination of the role of cytokines using gene deficient mice in African trypanosomiasis infection
title_full_unstemmed Determination of the role of cytokines using gene deficient mice in African trypanosomiasis infection
title_short Determination of the role of cytokines using gene deficient mice in African trypanosomiasis infection
title_sort determination of the role of cytokines using gene deficient mice in african trypanosomiasis infection
topic Immunology
url http://hdl.handle.net/11427/3119
work_keys_str_mv AT barkhuizenmark determinationoftheroleofcytokinesusinggenedeficientmiceinafricantrypanosomiasisinfection