Figure 2
CD40 surface expression levels on lipopolysaccharide (LPS)–activated dendritic cells. (A) Monocytes fractionated from peripheral blood mononuclear cells were stained with CD14, CD11c, and CD80 (green) and after 6 days of IL-4 and GM-CSF stimulation, a dendritic cell phenotype was observed (blue). (B) Monocyte-derived dendritic cells treated with (blue) and without (green) LPS were stained with CD40 antibody. A replicate experiment for the TNFRSF5 −1CT individual is shown (red) overlapping the previous experiment. (C) Representative plots of differences between lipopolysaccharide (LPS) untreated and treated CD40 peak levels (TNFRSF5 −1CC/−1CT n = 7, −1TT n = 4). Means (bars) with standard errors (boxes) and one SD (whiskers) are plotted. Data from −1CC and −1CT carriers were pooled due to similarities in their CD40 shifts.

CD40 surface expression levels on lipopolysaccharide (LPS)–activated dendritic cells. (A) Monocytes fractionated from peripheral blood mononuclear cells were stained with CD14, CD11c, and CD80 (green) and after 6 days of IL-4 and GM-CSF stimulation, a dendritic cell phenotype was observed (blue). (B) Monocyte-derived dendritic cells treated with (blue) and without (green) LPS were stained with CD40 antibody. A replicate experiment for the TNFRSF5 −1CT individual is shown (red) overlapping the previous experiment. (C) Representative plots of differences between lipopolysaccharide (LPS) untreated and treated CD40 peak levels (TNFRSF5 −1CC/−1CT n = 7, −1TT n = 4). Means (bars) with standard errors (boxes) and one SD (whiskers) are plotted. Data from −1CC and −1CT carriers were pooled due to similarities in their CD40 shifts.

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