Exposure of monocytes to B. anthracis capsule during differentiation alters the resulting iDCs' cytokine response to Ba PGN. Human monocytes were differentiated into iDCs in the presence of 500 μg/ml capsule or capA mutant preparation for 7 days. Control cells were differentiated in parallel in the absence of capsule. On day 7, the treated and naive control cells were stimulated with 1 μg/ml Ba PGN. Additional control cells were maintained unstimulated. On day 9, the media were analyzed for cytokines. Several donors exhibited decreased release of IL-6 (A), IL-10 (B), IL-1β (C), TNF-α (D), IFN-γ (E), and IL-23 (F) upon stimulation with Ba PGN (*, P < 0.05; **, P < 0.01; ***, P < 0.001; n = 2). P values for the responses to the two preparations (WT and capA mutant) were determined by comparing the mean pg/ml of each cytokine detected for the treated cells to the mean pg/ml of each cytokine detected for the control cells for each of four or five donors in a two-tailed t test. Data shown are from a representative donor.