Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/13826
Title: Effect of macrophage alone or primed with cytokines on Balamuthia mandrillaris interactions with human brain microvascular endothelial cells in vitro
Authors: Matin, Abdul
Nawaz, Salik
Jung, Suk-Yul
Keywords: Balamuthia mandrillaris
macrophages
cytokines
human brain microvascular endothelial cells
Balamuthia amoebic encephalitis
Issue Date: Nov-2018
Publisher: Pakistan Journal of Pharmaceutical Sciences University of Karachi
Citation: Matin, A., Siddiqui, R., Jung, S. Y., Kim, K. S., Stins, M., & Khan, N. A. (2007). Balamuthia mandrillaris interactions with human brain microvascular endothelial cells in vitro. Journal of medical microbiology, 56(8), 1110-1115.
Abstract: Balamuthia mandrillaris is well known to cause fatal Balamuthia amoebic encephalitis (BAE). Amoebic transmission into the central nervous system (CNS), haematogenous spread is thought to be the prime step, followed by blood–brain barrier (BBB) dissemination. Macrophages are considered to be the foremost line of defense and present in excessive numbers during amoebic infections. The aim of the present investigation was to evaluate the effects of macrophages alone or primed with cytokines on the biological characteristics of Balamuthia in vitro. Using human brain microvascular endothelial cells (HBMEC), which constitutes the BBB, we have shown that Balamuthia demonstrated >90% binding and >70% cytotoxicity to host cells. However, macrophages further increased amoebic binding and Balamuthia-mediated cell cytotoxicity. Furthermore macrophages exhibited no amoebicidal effect against Balamuthia. Zymography assay demonstrated that macrophages exhibited no inhibitory effect on proteolytic activity of Balamuthia. Overall we have shown for the first time macrophages has no inhibitory effects on the biological properties of Balamuthia in vitro. This also strengthened the concept that how and why Balamuthia can cause infections in both immuno-competent and immuno-compromised individuals.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/13826
ISSN: 1996-7195
Appears in Collections:Oct-Dec,2018,Issue(4)

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