A Low Interleukin-10 Tumor Necrosis Factor-α Ratio Is Associated with Malaria Anemia in Children Residing in a Holoendemic Malaria Region in Western Kenya

The balance between Th1 cytokines (tumor necrosis factor [TNF]-α, interferon [IFN]-γ) and Th2 cytokines (interleukin [IL]-10, -4) may be critical in the development of severe falciparum malaria. Therefore, plasma concentrations of these cytokines were determined in children with various manifestatio...

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Published in:The Journal of infectious diseases Vol. 179; no. 1; pp. 279 - 282
Main Authors: Othoro, Caroline, Lal, Altaf A., Nahlen, Bernard, Koech, Davy, Orago, Alloys S. S., Udhayakumar, Venkatachalam
Format: Journal Article
Language:English
Published: Chicago, IL University Chicago Press 01-01-1999
University of Chicago Press
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Summary:The balance between Th1 cytokines (tumor necrosis factor [TNF]-α, interferon [IFN]-γ) and Th2 cytokines (interleukin [IL]-10, -4) may be critical in the development of severe falciparum malaria. Therefore, plasma concentrations of these cytokines were determined in children with various manifestations of malaria. Plasma levels of IFN-γ and IL-4 were undetectable in most children. However, TNF-α and IL-10 were significantly elevated in children with high-density parasitemia and malaria anemia compared with children in control groups. In children with mild malaria, IL-10, but not TNF-α, was significantly elevated. While the highest concentrations of TNF-α were found in children with malaria anemia, IL-10 levels were highest in children with high-density uncomplicated malaria. The mean ratio of IL-10 to TNF-α was significantly higher in children with mild and high-density parasitemia (4.64, P <.005) than in children with malaria anemia (1.77). Thus, higher levels of IL-10 over TNF-α may prevent development of malaria anemia by controlling the excessive inflammatory activities of TNF-α.
Bibliography:ark:/67375/HXZ-4R405W0L-P
istex:54ED1113EE2AC6D6E4988DFD0731A1259EF98F07
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0022-1899
1537-6613
DOI:10.1086/314548