Fig. 1.
Fig. 1. Identification and distribution of peripheral blood DCs. / (A) PBMCs were gated and at least 50 000 events were acquired per sample. B cells, T cells, monocytes, and natural killer cells were detected with a cocktail of lineage-specific antibodies (lineage-marker) in FL-2. DCs were detected as lineage marker–negative cells with an isotype control antibody or anti–HLA-DR antibody in FL-1. Shown are examples of HLA-DR+ DCs in one healthy child (upper panel) and in 2 children suffering from severe malaria (middle and lower panels). (B) The boxplots indicate median and 25% and 75% percentiles for the percentage of CD83+ cells or HLA-DR+ DCs in healthy children and in children with severe or mild malaria. Outliers are indicated by open circles and extreme values are indicated by stars.

Identification and distribution of peripheral blood DCs.

(A) PBMCs were gated and at least 50 000 events were acquired per sample. B cells, T cells, monocytes, and natural killer cells were detected with a cocktail of lineage-specific antibodies (lineage-marker) in FL-2. DCs were detected as lineage marker–negative cells with an isotype control antibody or anti–HLA-DR antibody in FL-1. Shown are examples of HLA-DR+ DCs in one healthy child (upper panel) and in 2 children suffering from severe malaria (middle and lower panels). (B) The boxplots indicate median and 25% and 75% percentiles for the percentage of CD83+ cells or HLA-DR+ DCs in healthy children and in children with severe or mild malaria. Outliers are indicated by open circles and extreme values are indicated by stars.

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