Figure 1.
Phenotype of circulating IgM+λ+CD38high cells during KSHV-MCD flare. (A) P1 PBMCs were isolated using Ficoll gradient and stained using the method described in “Material and Methods.” At least 106 events were acquired. Gating strategy was performed as follows: (1) gating on single cells; (2) exclusion of T cells (CD3+) and monocytes (CD14+); (3) gating on IgM+CD38high cells; (4) gating on λ+ cells; and (5) assessment of CD19, CD20, CD24, CD27, and CD40 expression. Retrogating of the IgM+λ+CD38high population was performed on a side scatter/forward scatter (SSC/FSC) dot plot. Positivity threshold was determined on the fluorochrome corresponding isotype (depicted in blue). P1 is shown as a representative example. (B) Percentage of CD19, CD20, CD24, and CD27 positivity among IgM+λ+CD38high circulating cells detected in 14 patients with KSHV-MCD.

Phenotype of circulating IgM+λ+CD38high cells during KSHV-MCD flare. (A) P1 PBMCs were isolated using Ficoll gradient and stained using the method described in “Material and Methods.” At least 106 events were acquired. Gating strategy was performed as follows: (1) gating on single cells; (2) exclusion of T cells (CD3+) and monocytes (CD14+); (3) gating on IgM+CD38high cells; (4) gating on λ+ cells; and (5) assessment of CD19, CD20, CD24, CD27, and CD40 expression. Retrogating of the IgM+λ+CD38high population was performed on a side scatter/forward scatter (SSC/FSC) dot plot. Positivity threshold was determined on the fluorochrome corresponding isotype (depicted in blue). P1 is shown as a representative example. (B) Percentage of CD19, CD20, CD24, and CD27 positivity among IgM+λ+CD38high circulating cells detected in 14 patients with KSHV-MCD.

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