Figure 1
Figure 1. Abnormalities in peripheral cell homeostasis of HCV-MC vasculitis revert following rituximab. Naive (IgD+CD27−CD38low) lymphopenia (A), expansion of memory (IgD−CD27+CD38low) B cells (B) and plasmablasts (IgD−CD27highCD38high) (C), and quantitative deficiency of regulatory T cells CD4+CD25+FoxP3+ (D) in patients with mixed cryoglobulinemia (MC) vasculitis (MC pre-Rx) (n = 21) compared with healthy volunteers (Ctrls) (n = 15) and chronic HCV patients without MC-vasculitis (HCV Ctrls) (n = 20). Improvement of peripheral B- and T-cell abnormalities after rituximab in patients with MC vasculitis (MC post-Rx). Data are expressed as mean plus or minus SEM.

Abnormalities in peripheral cell homeostasis of HCV-MC vasculitis revert following rituximab. Naive (IgD+CD27CD38low) lymphopenia (A), expansion of memory (IgDCD27+CD38low) B cells (B) and plasmablasts (IgDCD27highCD38high) (C), and quantitative deficiency of regulatory T cells CD4+CD25+FoxP3+ (D) in patients with mixed cryoglobulinemia (MC) vasculitis (MC pre-Rx) (n = 21) compared with healthy volunteers (Ctrls) (n = 15) and chronic HCV patients without MC-vasculitis (HCV Ctrls) (n = 20). Improvement of peripheral B- and T-cell abnormalities after rituximab in patients with MC vasculitis (MC post-Rx). Data are expressed as mean plus or minus SEM.

Close Modal

or Create an Account

Close Modal
Close Modal