Figure 5
Figure 5. Representative expression of CD27, CD138, and surface IgD, IgG, and IgA on lymphogated cells in patients with CVID or IgAD. Cell surface expression of these markers is presented in panels A and C for CVID patients and in panels B and D for subjects with IgAD on a 4-decade log scale as dot plots of correlated x-axis and y-axis fluorescence. FCM analysis was performed at days 0, 3, 5 (and 7), with PBMCs cultured in the presence of IL-21 (10 ng/mL), IL-4 (0.5 ng/mL), and anti–human CD40 mAb (2 μg/mL). (A-B) Quadrant markers were positioned to include naive mature B cells (UL), natural effector B cells (UR), and IgD− memory B cells (LR). The circle tags a population of CD27high IgD− B cells. (C) Quadrant markers were positioned to separate CD138+ plasma cells (UL) from sIgG+ B cells (LR). (D) Regions were positioned to separate CD138+ plasma cells (UL) from sIgA+ B cells (LR).

Representative expression of CD27, CD138, and surface IgD, IgG, and IgA on lymphogated cells in patients with CVID or IgAD. Cell surface expression of these markers is presented in panels A and C for CVID patients and in panels B and D for subjects with IgAD on a 4-decade log scale as dot plots of correlated x-axis and y-axis fluorescence. FCM analysis was performed at days 0, 3, 5 (and 7), with PBMCs cultured in the presence of IL-21 (10 ng/mL), IL-4 (0.5 ng/mL), and anti–human CD40 mAb (2 μg/mL). (A-B) Quadrant markers were positioned to include naive mature B cells (UL), natural effector B cells (UR), and IgD memory B cells (LR). The circle tags a population of CD27high IgD B cells. (C) Quadrant markers were positioned to separate CD138+ plasma cells (UL) from sIgG+ B cells (LR). (D) Regions were positioned to separate CD138+ plasma cells (UL) from sIgA+ B cells (LR).

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