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Reciprocal Regulation of Th1- and Th2-Cytokine-Producing T Cells during Clearance of Parasitemia in Plasmodium falciparum Malaria
Authors:Stefan Winkler   Martin Willheim   Karin Baier   Daniela Schmid   Alexander Aichelburg   Wolfgang Graninger     Peter G. Kremsner
Affiliation:Department of Internal Medicine, Division of Infectious Diseases,1. and Institute of General and Experimental Pathology,3. University of Vienna, Vienna, Austria; Research Unit of the Albert Schweitzer Hospital, Lambaréné, Gabon2.; and Department of Parasitology, Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany4.
Abstract:Flow cytometry for the intracellular detection of T-cell cytokines was performed for 15 Gabonese patients during acute uncomplicated Plasmodium falciparum malaria. A striking expansion of CD4+ and CD8+ T cells producing gamma interferon (IFN-γ) was found during drug-induced clearance of parasitemia, paralleled by a decrease of interleukin-2 (IL-2) production. The frequency of IL-4- and IL-13-producing CD4+ cells gradually decreased, whereas the frequency of T cells producing IL-2+–IFN-γ+, IL-4–IL-5+, and IL-4+–IL-5+ cytokines as well as IL-4+–IFN-γ+ and IL-13+–IFN-γ+ cytokines was not significantly altered. The capacity for IL-10 production within the CD4+ subset increased due to an expansion of both IL-10+–IFN-γ and IL-10+–IFN-γ+ cytokine-expressing cells. Thus, a more pronounced Th2-driven immune response during acute untreated P. falciparum infection with a shift towards Th1 responsiveness induced by parasite clearance is suggested.
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