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. 2018 Feb 16;19(2):589. doi: 10.3390/ijms19020589

Figure 1.

Figure 1

B-cell differentiation subsets in patients with primary antiphospholipid syndrome (pAPS), patients with systemic lupus erythematosus (SLE), and healthy controls (HC). Percentages of different B-cell subsets: transitional-immature (CD19+CD5+CD10+ CD27IgD++ CD24hi CD38hi), naïve (CD19+ CD5+/− CD10 CD27IgD+ CD24int CD38low/), non-switched memory (CD19+ CD27+ IgD+ CD38 IgM+), double-negative (CD19+ CD27IgD CD24 CD38−/+ IgM), switched memory (CD19+ CD27+IgD CD38+IgM+/−), and plasma cells(CD19lo CD27hiIgD CD38hi CD138−/+) in HC and in patients with pAPS or SLE. CD19+ cells were gated for analysis. Box plots show the median and interquartile range. Differences were significant when p value <0.05 by Mann–Whitney U test. HC: healthy controls; pAPS: primary antiphospholipid syndrome; SLE: systemic lupus erythematosus.