Figure 6
Figure 6. Patients with cGVHD have defective CD24hiCD27+ and plasmablast-like IL-10–producing B-cell compartments. Whole PBMCs were cultured for 66 hours with CpG-B (3 μg/mL, left panel) followed by restimulation with PMA + ionomycin in the presence of brefeldin A the last 5 hours of culture, fixed, permeabilized, and intracellular IL-10 was measured in live B-cell subsets by flow cytometry. (A) Proportions of CD19+CD24hiCD27+IL-10+ cells in percentages of live CD19+CD24hiCD27+ cells in healthy donors, patients with active cGVHD, cGVHD in remission, and AHSCT recipients with no history of cGVHD. (B) Proportions of CD19+CD24−CD38hiIL-10+ plasmablast-like cells in percentages of live CD19+CD24−CD38hi cells in healthy donors, patients with active cGVHD, cGVHD in remission, and AHSCT recipients with no history of cGVHD.

Patients with cGVHD have defective CD24hiCD27+ and plasmablast-like IL-10–producing B-cell compartments. Whole PBMCs were cultured for 66 hours with CpG-B (3 μg/mL, left panel) followed by restimulation with PMA + ionomycin in the presence of brefeldin A the last 5 hours of culture, fixed, permeabilized, and intracellular IL-10 was measured in live B-cell subsets by flow cytometry. (A) Proportions of CD19+CD24hiCD27+IL-10+ cells in percentages of live CD19+CD24hiCD27+ cells in healthy donors, patients with active cGVHD, cGVHD in remission, and AHSCT recipients with no history of cGVHD. (B) Proportions of CD19+CD24CD38hiIL-10+ plasmablast-like cells in percentages of live CD19+CD24CD38hi cells in healthy donors, patients with active cGVHD, cGVHD in remission, and AHSCT recipients with no history of cGVHD.

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