Fig 1: FcR profiles and effect of FcR interaction on mycobacterial growth control(A) FcR expression (CD16, CD32, CD64, and CD89) on monocytes, B cells and NK/NKT cells (n = 8–11 healthy individuals) was assessed by flow cytometry. Boolean gating was applied according to the matrix displayed at the x axis and percentage of positive cells is depicted as bars (median with range) with individual measurements as dots on the y axis.(B) Monocytes are further subtyped into classical, intermediate and non-classical based on their CD14 and CD16 expression.(C) For each monocyte subset Boolean gating for FcRs was applied as in (A). Black dots (A–C) represent the PBMCs used for the MGIA as displayed in Figure 2B.(D) Bar chart (mean with SD) representing the total FcRs expressed on the monocytes of the PBMCs used for MGIA (upper panel) or on non-classical monocytes (lower panel).