Abstract

ObjectivesB cell depletion by rituximab (RTX) is an effective treatment for anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV). However, peripheral B cell phenotypes and the selection criteria for RTX therapy in AAV remain unclear.MethodsPhenotypic characterization of circulating B cells was performed by 8-color flow cytometric analysis in 54 newly diagnosed AAV patients (20 granulomatosis with polyangiitis and 34 microscopic polyangiitis). Patients were considered eligible to receive intravenous cyclophosphamide pulse (IV-CY) or RTX. All patients also received high-dose glucocorticoids (GC). We assessed circulating B cell phenotypes and evaluated the efficacy after 6 months of treatment.ResultsThere were no significant differences in the rate of clinical improvement, relapses, or serious adverse events between patients receiving RTX and IV-CY. The rate of Birmingham Vasculitis Activity Score (BVAS) improvement at 6 months tended to be higher in the RTX group than in the IV-CY group. The proportion of effector or class-switched memory B cells increased in 24 out of 54 patients (44%). The proportions of peripheral T and B cell phenotypes did not correlate with BVAS at baseline. However, among peripheral B cells, the proportion of class-switched memory B cells negatively correlated with the rate of improvement in BVAS at 6 months after treatment initiation (r = − 0.28, p = 0.04). Patients with excessive B cell differentiation were defined as those in whom the proportion of class-switched memory B cells or IgD−CD27− B cells among all B cells was > 2 SDs higher than the mean in the HCs. The rate of BVAS remission in patients with excessive B cell differentiation was significantly lower than that in patients without. In patients with excessive B cell differentiation, the survival rate, the rate of BVAS-remission, and dose reduction of GC were significantly improved in the RTX group compared to those in the IV-CY group after 6 months of treatment.ConclusionsThe presence of excessive B cell differentiation was associated with treatment resistance. However, in patients with circulating B cell abnormality, RTX was effective and increased survival compared to IV-CY. The results suggest that multi-color flow cytometry may be useful to determine the selection criteria for RTX therapy in AAV patients.

Highlights

  • Anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) is a systemic autoimmune disease with poor prognosis that damages various organs and commonly occurs in the elderly [1]

  • The efficacy of B cell depletion therapy has been demonstrated in AAV patients by the Rituximab in ANCA-Associated Vasculitis (RAVE) trial [3] and the Randomized Trial of Rituximab Versus Cyclophosphamide for ANCA-Associated Renal Vasculitis (RITUXVAS) [4] trial

  • The patients were divided into those receiving high-dose GC therapy combined with RTX (RTX group) and those receiving GC therapy combined with intravenous CY pulse (IV-CY group)

Read more

Summary

Introduction

Anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) is a systemic autoimmune disease with poor prognosis that damages various organs and commonly occurs in the elderly [1]. AAV is treated with high-dose glucocorticoid (GC) therapy combined with cyclophosphamide (CY), azathioprine (AZA), etc. The efficacy of B cell depletion therapy has been demonstrated in AAV patients by the Rituximab in ANCA-Associated Vasculitis (RAVE) trial [3] and the Randomized Trial of Rituximab Versus Cyclophosphamide for ANCA-Associated Renal Vasculitis (RITUXVAS) [4] trial. Rituximab (RTX) has been shown to be as effective as CY for inducing remission in AAV patients. It is unknown how B cells affect disease activity and prognosis in AAV patients. RTX, which is the first biologic drug approved for the treatment of AAV, has a specific action mechanism of depleting B cells, the differential use of RTX and CY remains a major clinical question

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call