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The neuroimmune response to cryptococcal infection

Cryptococcal meningitis (CM) is a fatal fungal infection of the brain that is responsible for up to 20% of all AIDS-related deaths globally, 75% of which are from Sub-Saharan Africa. CM is characterised by debilitating neurological damage often resulting in death or serious longterm sequelae even af...

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Main Author: Kauchali, Maahir
Other Authors: Dangarembizi, Rachael
Format: Thesis
Language:English
Published: Department of Human Biology 2024
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access_status_str Open Access
author Kauchali, Maahir
author2 Dangarembizi, Rachael
author_browse Dangarembizi, Rachael
Kauchali, Maahir
author_facet Dangarembizi, Rachael
Kauchali, Maahir
author_sort Kauchali, Maahir
collection Thesis
description Cryptococcal meningitis (CM) is a fatal fungal infection of the brain that is responsible for up to 20% of all AIDS-related deaths globally, 75% of which are from Sub-Saharan Africa. CM is characterised by debilitating neurological damage often resulting in death or serious longterm sequelae even after receiving treatment. Despite the brain being the main organ of injury, there is a paucity of data describing the interaction of the fungus with resident immune cells of the brain. The aim of this study was to investigate the neuroimmune response to cryptococcal infection using a novel organotypic brain slice culture system. We treated cultured brain slices with either whole cell C. neoformans, its purified capsule (a known major virulent factor) or lipopolysaccharide (LPS), and compared them to untreated control slices. The neuroimmune response was measured by tracking the activation of nuclear factor for interleukin 6 (NF-IL6), and confirmed by measuring the release of IL6 and tumour necrosis factor- (TNF-α). Our results showed that neither C. neoformans nor its purified capsule elicited a neuroinflammatory response as observed in LPS-treated slices. Co-stimulation of LPS-treated slices with C. neoformans or its purified capsule did not abolish an LPS-induced inflammatory responses in brain slices. Our findings also show that microglia are the principal cells that phagocytose fungal cells during cryptococcal infection and that even after engulfing fungal cells, microglial cells were not classically activated. Therefore, we concluded that C. neoformans recognition by resident immune cells, on its own, may not be responsible for the debilitating inflammatory response observed during CM, and that the purified cryptococcal capsule does not elicit an inflammatory or anti-inflammatory response.
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institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:57.328Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2024
publishDateRange 2024
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spelling oai:open.uct.ac.za:11427/39582 The neuroimmune response to cryptococcal infection Kauchali, Maahir Dangarembizi, Rachael Raimondo Joseph Medicine Cryptococcal meningitis (CM) is a fatal fungal infection of the brain that is responsible for up to 20% of all AIDS-related deaths globally, 75% of which are from Sub-Saharan Africa. CM is characterised by debilitating neurological damage often resulting in death or serious longterm sequelae even after receiving treatment. Despite the brain being the main organ of injury, there is a paucity of data describing the interaction of the fungus with resident immune cells of the brain. The aim of this study was to investigate the neuroimmune response to cryptococcal infection using a novel organotypic brain slice culture system. We treated cultured brain slices with either whole cell C. neoformans, its purified capsule (a known major virulent factor) or lipopolysaccharide (LPS), and compared them to untreated control slices. The neuroimmune response was measured by tracking the activation of nuclear factor for interleukin 6 (NF-IL6), and confirmed by measuring the release of IL6 and tumour necrosis factor- (TNF-α). Our results showed that neither C. neoformans nor its purified capsule elicited a neuroinflammatory response as observed in LPS-treated slices. Co-stimulation of LPS-treated slices with C. neoformans or its purified capsule did not abolish an LPS-induced inflammatory responses in brain slices. Our findings also show that microglia are the principal cells that phagocytose fungal cells during cryptococcal infection and that even after engulfing fungal cells, microglial cells were not classically activated. Therefore, we concluded that C. neoformans recognition by resident immune cells, on its own, may not be responsible for the debilitating inflammatory response observed during CM, and that the purified cryptococcal capsule does not elicit an inflammatory or anti-inflammatory response. The neuroimmune response to cryptococcal infection 2024-05-06T13:56:46Z 2024-05-06T13:56:46Z 2023 2024-05-06T13:23:54Z Thesis / Dissertation Masters MSc http://hdl.handle.net/11427/39582 eng application/pdf Department of Human Biology Faculty of Health Sciences University of Cape Town
spellingShingle Medicine
Kauchali, Maahir
The neuroimmune response to cryptococcal infection
thesis_degree_str Master's
title The neuroimmune response to cryptococcal infection
title_full The neuroimmune response to cryptococcal infection
title_fullStr The neuroimmune response to cryptococcal infection
title_full_unstemmed The neuroimmune response to cryptococcal infection
title_short The neuroimmune response to cryptococcal infection
title_sort neuroimmune response to cryptococcal infection
topic Medicine
url http://hdl.handle.net/11427/39582
work_keys_str_mv AT kauchalimaahir theneuroimmuneresponsetocryptococcalinfection
AT kauchalimaahir neuroimmuneresponsetocryptococcalinfection