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Severe malarial anemia associated with increased soluble Fas ligand (sFasL) concentrations in Gabonese children.

Abstract
To investigate if severe malarial anemia is associated with specific cytokine overproduction, we evaluated serum levels of soluble Fas ligand (sFasL), tumor necrosis factor (TNF-alpha) and interleukin-10 (IL-10) from three groups of young children with Plasmodium falciparum infection (asymptomatic cases, uncomplicated malaria cases and severe malarial anemia cases), in a hyperendemic area of Gabon. In uncomplicated cases, only TNF levels were significantly (p < 0.001) increased in comparison to asymptomatic cases with P. falciparum infection. High levels of sFasL, TNF-alpha and IL-10 were associated with low hemoglobin concentrations, sFasL levels were significantly higher in children with severe malarial anemia (p < 0.001) as compared to both other groups. The parasite density was positively correlated with IL-10, TNF-alpha and sFasL levels. TNF-alpha and sFasL, but not IL-10 or parasitemia, were independent predictors of hemoglobin concentrations. These results suggest that, in malaria, a specific dysregulation of the cytokine balance may lead to complications such as severe anemia.
AuthorsSaadou Issifou, Elie Mavoungou, Steffen Borrmann, Marielle K Bouyou-Akotet, Pierre-Blaise Matsiegui, Peter G Kremsner, Francine Ntoumi
JournalEuropean cytokine network (Eur Cytokine Netw) 2003 Oct-Dec Vol. 14 Issue 4 Pg. 238-41 ISSN: 1148-5493 [Print] France
PMID14715416 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright John Libbey Eurotext 2003.
Chemical References
  • FASLG protein, human
  • Fas Ligand Protein
  • Membrane Glycoproteins
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
Topics
  • Acute Disease
  • Anemia (etiology, immunology, metabolism)
  • Animals
  • Child
  • Child, Preschool
  • Fas Ligand Protein
  • Female
  • Gabon
  • Humans
  • Infant
  • Inflammation (metabolism)
  • Interleukin-10 (blood)
  • Malaria, Falciparum (immunology, metabolism)
  • Male
  • Membrane Glycoproteins (blood)
  • Plasmodium falciparum (immunology)
  • Tumor Necrosis Factor-alpha (metabolism)

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