¹Aix-Marseille université, IFR 48, Faculté de Pharmacie, Laboratoire de Pharmacogénétique des Maladies Parasitaires, Marseille, France

Correspondence: Dr P Rihet, Aix-Marseille université, IFR 48, Faculté de Pharmacie, Laboratoire de Pharmacogénétique des Maladies Parasitaires-EA 864, 27 Bd Jean Moulin 13385 Marseille Cedex 5, France. E-mail: rihet@luminy.univ-mrs.fr

Received 13 February 2008; Revised 25 March 2008; Accepted 25 March 2008; Published online 1 May 2008.

Abstract

Chromosome 5q31–q33 has been linked to Plasmodium falciparum parasitemia in several independent studies. This chromosomal region contains numerous immunoregulatory genes. Among these, IL12B that encodes the p40 subunit of interleukin-12 (IL-12) appeared to be a promising functional candidate gene, and IL12Bpro, a promoter polymorphism, was associated with mortality from severe malaria in children. In this study, we characterized genetic variation in IL12B in 215 individuals belonging to 34 families and evaluated linkage and association of parasitemia with IL12B polymorphisms and haplotypes. We searched for IL12B polymorphisms in the coding regions and the corresponding intron–exon borders. We also examined IL12Bpro and IL12B 3'untranslated region (UTR) polymorphisms, which are thought to influence the production of IL-12. We showed a high level of conservation of IL12B-coding regions and identified five polymorphisms in introns and the two polymorphisms in the promoter and the 3'UTR regions. Although IL12B polymorphisms were linked to parasitemia, there was association of parasitemia with neither polymorphisms nor haplotypes. We cannot exclude that an unknown IL12B cis-regulatory element polymorphism affects both IL-12 production and parasitemia. However, our results suggest that genetic variation in IL12B does not explain differences in parasitemia in individuals living in an endemic area.