Figure 1
Figure 1. Phenotype and proliferative responses of CD21low and CD21high VH1-69+ B cells. (A-B) FACS plots from a representative (n = 8) MC patient with predominance of CD21low VH1-69+ B cells. (A) Expression of surface markers by electronically gated VH1-69+ B cells stained with the G6 antibody.4 (B) Gating strategy for the analysis of proliferative responses of VH1-69+ and VH1-69− B cells to CpG (2.5 μg/mL, 5-day culture). Cells were permeabilized before staining. The regions of analysis encompass CD20+ B cells and CD20low/neg plasmablasts, which were also characterized as CD38+ cytoplasmic-IgMhigh cells (not shown). Plasmablasts are present only in the VH1-69− gating region. Percent values in the histograms denote the number of cells entering division (precursor cohort5). (C-D) FACS plots from a representative (n = 3) MC patient with highly enriched CD21high VH1-69+ B cells. Analyses of surface marker expression (C) and of proliferative responses to CpG (D) were done as in panels A and B, respectively.

Phenotype and proliferative responses of CD21low and CD21high VH1-69+ B cells. (A-B) FACS plots from a representative (n = 8) MC patient with predominance of CD21low VH1-69+ B cells. (A) Expression of surface markers by electronically gated VH1-69+ B cells stained with the G6 antibody. (B) Gating strategy for the analysis of proliferative responses of VH1-69+ and VH1-69 B cells to CpG (2.5 μg/mL, 5-day culture). Cells were permeabilized before staining. The regions of analysis encompass CD20+ B cells and CD20low/neg plasmablasts, which were also characterized as CD38+ cytoplasmic-IgMhigh cells (not shown). Plasmablasts are present only in the VH1-69 gating region. Percent values in the histograms denote the number of cells entering division (precursor cohort). (C-D) FACS plots from a representative (n = 3) MC patient with highly enriched CD21high VH1-69+ B cells. Analyses of surface marker expression (C) and of proliferative responses to CpG (D) were done as in panels A and B, respectively.

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