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Fig. 2 | Arthritis Research & Therapy

Fig. 2

From: Integrative analysis reveals CD38 as a therapeutic target for plasma cell-rich pre-disease and established rheumatoid arthritis and systemic lupus erythematosus

Fig. 2

CD38 expression on immune cells in peripheral blood mononuclear cells (PBMC) from healthy donors and patients with systemic lupus erythematosus (SLE) or rheumatoid arthritis (RA). a Gating strategy for plasma cells and plasmablasts in PBMC samples. Plasma cells are gated as live singlet lymphocytes, CD3−CD56−CD19low/midCD20−CD38hiCD27hiCD138+. Plasmablasts are gated as live singlet lymphocytes, CD3−CD56−CD19low/midCD20−CD38hiCD27hiCD138−. CD19hi B cells are separated into naïve B cell (IgD+CD27−), non-class-switched memory B cell (CD27+IgD+), class-switched memory B cell (CD27+IgD−) and CD27− memory B cell (CD27−IgD−). b Percentage of CD27hiCD38hiCD138+ plasma cells in total lymphocytes from PBMCs from healthy controls and patients with SLE or RA. c Percentage of CD27hiCD38hiCD138− plasmablasts in total lymphocytes from PBMCs from different groups. d-f Percentage of class-switched memory cell (d), CD27− memory B cell (e), and non-class-switched memory B cell (f) in total lymphocytes. g Quantification of CD38 MFI in naïve B cell, non-class switched memory cell, class-switched memory cell, CD27− memory cell, plasma cells and plasmablasts

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