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. 2015 Aug 12;83(9):3732–3739. doi: 10.1128/IAI.00473-15

FIG 2.

FIG 2

Kinetics of APC subset frequencies and expression of activation markers during and after CHMI. (A) Kinetics of APC subset frequency (percentages of viable PBMCs). (B) Kinetics of HLA-DR expression (geometric mean fluorescence intensity [MFI]) of the six APC subsets. (C) Kinetics of CD86 expression (MFI) of the six APC subsets. Data are presented for each individual donor (gray dots) and as means (n = 15) with standard errors of the means (SEM) (black error bars). *, P < 0.05; **, P < 0.01; ***, P < 0.001 (one-way ANOVA with Dunnett's post hoc test compared to baseline [C −1]). Inclusion of the outlier (black square) in the CD1c mDC frequency in the statistical analysis renders the increase on the DT significant. C, challenge; DT, day of treatment.