In other experiments, whole PBMC were depleted of individual leukocyte subpopulations by magnetic beads specific for CD3ε,γδTCR selleck chemicals llc or CD56 (Miltenyi Biotech, Utrecht, The Netherlands) according to the manufacturer’s instructions. Depleted PBMC were cultured at a concentration equating to 2.5×106 whole PBMC/mL. Undepleted control PBMC in these experiments were treated similarly, i.e. also passed over a magnetic column. Efficiency of depletion was assessed in a subset of donors by flow cytometry and was consistently >90, >90 and >95%, respectively. In a subset
of these experiments, exogenous recombinant human IL-2 was added immediately prior to stimulation at final concentrations up to 100 IU/mL. As a control, similar depletion experiments were performed on PBMC from a representative sample of malaria-naïve Caucasian donors, Caucasians who have regularly visited malaria-endemic areas under chemoprophylaxis and
semi-immune African adults. For the latter group, PBMC were collected from healthy adult Metformin price male volunteers in the Koro district of Mali as part of ongoing investigational studies into interethnic differences in susceptibility to malaria 26. Samples for which data are presented here were collected during the 2008 dry season (April). Approval for the study was provided by the institutional review board of the University of Bamako (No. 0527/FMPOS). Following 24-h in vitro stimulation (last 4 h with 10 μg/mL brefeldin A), PBMC were stained for surface markers and intracellular IFN-γ using Fix & Perm reagents (Caltag Laboratories, Carlsbad, CA, USA) according to the manufacturer’s instructions and read on a FACScalibur flow cytometer. The following fluorescent mAb were used: CD3-PerCP, CD25-APC (BD Biosciences, San Jose, CA, USA), IFN-γ-FITC, mouse IgG1 isotype-FITC, IL-2-APC, CD56-PE and CD56-APC (all Ebioscience, Uithoorn, The Netherlands). IFN-γ production in supernatant was measured by sandwich ELISA (Sanquin, Amsterdam, The Netherlands), according to the manufacturer’s instructions.
Nonparametric Dipeptidyl peptidase tests (Wilcoxon, Spearman and Friedman) were used in all analyses; p-values<0.05 were considered statistically significant. Foremost, the authors acknowledge the volunteers who took part in this study, for their time and enthusiasm. The authors thank J. Wiersma for clinical assistance during the trial and are indebted to M. v. d. Vegte and G. J. v. Gemert for culturing P. falciparum-infected erythrocytes and generating infected mosquitoes. Financial support for this study was provided by the Dioraphte foundation (VSM Malaria, project no. 06-03-08-00). M. B. B. M. is supported by a European Union FP6 Network of Excellence (BioMalPar) fellowship. Conflict of interest: The authors declare no financial or commercial conflict of interest.