Fig. 2From: Integrative analysis reveals CD38 as a therapeutic target for plasma cell-rich pre-disease and established rheumatoid arthritis and systemic lupus erythematosusCD38 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 plasmablastsBack to article page