Open Access

ARTICLE

Natural killer (NK) cell-mediated cytolysis of Plasmodium falciparum-infected human red blood cells in vitro

Elie Mavoungou^1,2, Adrian J. F. Luty^1,2, Peter G. Kremsner^1,2

1 Department of Parasitology, Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany and
2 Medical Research Unit, Albert Schweitzer Hospital, Lambaréné, Gabon.

* Corresponding Author: E. Mavoungou,

European Cytokine Network 2003, 14(3), 134-142.

Abstract

The ability of human NK cells to inhibit the growth in vitro of the asexual blood stages of Plasmodium falciparum was tested. Purified NK cells from donors with no prior exposure to malaria significantly inhibited parasite growth after 48 hours of co-culture in the presence of human immune serum. This inhibition was completely abrogated by pre-treatment of the NK cells with an anti-CD95 (anti-Fas) monoclonal antibody and human Fas-Fc soluble protein. The level of growth inhibition was also substantially reduced by pre-treatment with an anti-CD56 antibody. These two antibodies caused reductions, to varying levels, of the amounts of NK cell-derived granzyme B (GrB) and pro-inflammatory cytokines, but only the anti-CD95 antibody affected the production of soluble Fas ligand (sFasL). Direct destruction of parasite-infected red cells by NK cells, in the absence of serum, was also observed in a standard 51 Cr cytotoxicity test, during which N-carboxybenzoxy-L-lysine thiobenzil ester (BLT esterase) activity, which catalyzes serine protease granule release, was detected. The results obtained are indicative of a novel mechanism of NK cell-mediated cytotoxic activity against Plasmodium falciparum-infected red cells, which is mediated in part by both Fas and by GrB.

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