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A study of the immune response in murine experimental malaria, with special reference to the effects of South African medicinal plants, artesunate and chloroquine

The role of pro-inflarrnnatory cytokines (TNF and IFN-y) in a murine experimental malaria model for cerebral malaria is reported in this thesis. Wild type and receptor knockout mice (IFN-y deficient mice (IFN-l") and TNF-a/fr1- double deficient) were infected with Plasmodium berghei ANKA {PbA). PbA...

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Main Author: Gumede, Bonginkosi
Other Authors: Folb, Peter
Format: Thesis
Language:English
English
Published: Division of Clinical Pharmacology 2025
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access_status_str Open Access
author Gumede, Bonginkosi
author2 Folb, Peter
author_browse Folb, Peter
Gumede, Bonginkosi
author_facet Folb, Peter
Gumede, Bonginkosi
author_sort Gumede, Bonginkosi
collection Thesis
description The role of pro-inflarrnnatory cytokines (TNF and IFN-y) in a murine experimental malaria model for cerebral malaria is reported in this thesis. Wild type and receptor knockout mice (IFN-y deficient mice (IFN-l") and TNF-a/fr1- double deficient) were infected with Plasmodium berghei ANKA {PbA). PbA induced fatal cerebral malaria in wild type mice, which died within 5 to 8 days. In contrast, IFN-f1- and TNF-a/[r1-were completely resistant to PbA-induced cerebral malaria. Both wild type and mutant mice developed a similar degree of parasitaemia in the initial phase, and anaemia and leukocytosis were not different, showing that both anaemia and mobilisation of leukocytes occur in the absence of TNF and IFN-y. The results show that TNF'- and IFN,f'- mice are resistant to PbA-induced cerebral malaria, and confirm the role played by Thl cytokines in its pathogenesis. Plasmodium chabaudi chabaudi AS infection results in splenomegaly, and activation of the immune system. Resistant C57BL/6 mice, which eliminate the parasites and survive the infection, developed marked splenomegaly. Susceptible A/J mice develop minimal splenomegaly. In this work it has been shown that there is a rapid deterioration in splenic architecture, although immunohistochemistry confirmed preservation of a high level of structure and organisation. CD 11 c {dendritic) cells moved from the marginal zone into the CD4+ T cell area (where their antigen presenting function would be maximal). The juxtaposition of CDllc and T cells might be associated with immune complex formation in the spleen during the infection. The findings were similar for C57BL/6 and A/J mice. A 14-day course of artesunate 100 mg/kg prevented completely the development of parasitaemia and cerebral malaria in Plasmodium berghei ANKA infected mice, with survival of more than 60d. Chloroquine enhanced production of IL-10. Artesunate displayed enhanced IL-1 0 activity but no effect on production of pro-inflammatory cytokines. Extracts of W. salutaris, a South African medicinal plant, reduced parasitaemia by >50% at doses of 100 and 500mg/kg, and of A. annua reduced parasitaemia by 64% at a dose of 200 mg/kg. These extracts, and extracts of H. procumbens, had immunomodulatory activity on TNF-a., IFN-y, IL-12 and IL-10 production by Con A- and LPS-induced splenocytes.
format Thesis
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institution University of Cape Town (South Africa)
language English
eng
last_indexed 2026-06-10T12:32:21.936Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2025
publishDateRange 2025
publishDateSort 2025
publisher Division of Clinical Pharmacology
publisherStr Division of Clinical Pharmacology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/42033 A study of the immune response in murine experimental malaria, with special reference to the effects of South African medicinal plants, artesunate and chloroquine Gumede, Bonginkosi Folb, Peter Ryffel, Bernhard Malaria Medicinal plants South African The role of pro-inflarrnnatory cytokines (TNF and IFN-y) in a murine experimental malaria model for cerebral malaria is reported in this thesis. Wild type and receptor knockout mice (IFN-y deficient mice (IFN-l") and TNF-a/fr1- double deficient) were infected with Plasmodium berghei ANKA {PbA). PbA induced fatal cerebral malaria in wild type mice, which died within 5 to 8 days. In contrast, IFN-f1- and TNF-a/[r1-were completely resistant to PbA-induced cerebral malaria. Both wild type and mutant mice developed a similar degree of parasitaemia in the initial phase, and anaemia and leukocytosis were not different, showing that both anaemia and mobilisation of leukocytes occur in the absence of TNF and IFN-y. The results show that TNF'- and IFN,f'- mice are resistant to PbA-induced cerebral malaria, and confirm the role played by Thl cytokines in its pathogenesis. Plasmodium chabaudi chabaudi AS infection results in splenomegaly, and activation of the immune system. Resistant C57BL/6 mice, which eliminate the parasites and survive the infection, developed marked splenomegaly. Susceptible A/J mice develop minimal splenomegaly. In this work it has been shown that there is a rapid deterioration in splenic architecture, although immunohistochemistry confirmed preservation of a high level of structure and organisation. CD 11 c {dendritic) cells moved from the marginal zone into the CD4+ T cell area (where their antigen presenting function would be maximal). The juxtaposition of CDllc and T cells might be associated with immune complex formation in the spleen during the infection. The findings were similar for C57BL/6 and A/J mice. A 14-day course of artesunate 100 mg/kg prevented completely the development of parasitaemia and cerebral malaria in Plasmodium berghei ANKA infected mice, with survival of more than 60d. Chloroquine enhanced production of IL-10. Artesunate displayed enhanced IL-1 0 activity but no effect on production of pro-inflammatory cytokines. Extracts of W. salutaris, a South African medicinal plant, reduced parasitaemia by >50% at doses of 100 and 500mg/kg, and of A. annua reduced parasitaemia by 64% at a dose of 200 mg/kg. These extracts, and extracts of H. procumbens, had immunomodulatory activity on TNF-a., IFN-y, IL-12 and IL-10 production by Con A- and LPS-induced splenocytes. 2025-10-24T08:39:57Z 2025-10-24T08:39:57Z 2003 2025-10-24T08:21:01Z Thesis / Dissertation Doctoral PhD http://hdl.handle.net/11427/42033 en eng application/pdf Division of Clinical Pharmacology Faculty of Health Sciences University of Cape Town
spellingShingle Malaria
Medicinal plants
South African
Gumede, Bonginkosi
A study of the immune response in murine experimental malaria, with special reference to the effects of South African medicinal plants, artesunate and chloroquine
thesis_degree_str Doctoral
title A study of the immune response in murine experimental malaria, with special reference to the effects of South African medicinal plants, artesunate and chloroquine
title_full A study of the immune response in murine experimental malaria, with special reference to the effects of South African medicinal plants, artesunate and chloroquine
title_fullStr A study of the immune response in murine experimental malaria, with special reference to the effects of South African medicinal plants, artesunate and chloroquine
title_full_unstemmed A study of the immune response in murine experimental malaria, with special reference to the effects of South African medicinal plants, artesunate and chloroquine
title_short A study of the immune response in murine experimental malaria, with special reference to the effects of South African medicinal plants, artesunate and chloroquine
title_sort study of the immune response in murine experimental malaria with special reference to the effects of south african medicinal plants artesunate and chloroquine
topic Malaria
Medicinal plants
South African
url http://hdl.handle.net/11427/42033
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