Targeting B lymphocytes as therapy for ANCA-associated vasculitis

Rheum Dis Clin North Am. 2007 Nov;33(4):741-54, v. doi: 10.1016/j.rdc.2007.09.001.

Abstract

This article focuses on the initial results achieved with the more selective immunosuppressive approach of B-lymphocyte depletion in patients who fail cyclophosphamide or have contraindications for its use in the treatment of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). This novel approach has sparked hope for patients and physicians in their search for effective, well-tolerated therapy for AAV. B-cell depletion is now undergoing rigorous investigation in randomized clinical trials.

Publication types

  • Review

MeSH terms

  • Antibodies, Antineutrophil Cytoplasmic
  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Monoclonal, Humanized
  • Antibodies, Monoclonal, Murine-Derived
  • Antirheumatic Agents / therapeutic use
  • B-Cell Activating Factor / drug effects
  • B-Lymphocytes / drug effects*
  • B-Lymphocytes / immunology
  • Churg-Strauss Syndrome / drug therapy
  • Churg-Strauss Syndrome / immunology
  • Granulomatosis with Polyangiitis / drug therapy
  • Granulomatosis with Polyangiitis / immunology
  • Rituximab
  • Vasculitis / drug therapy*
  • Vasculitis / immunology

Substances

  • Antibodies, Antineutrophil Cytoplasmic
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Antibodies, Monoclonal, Murine-Derived
  • Antirheumatic Agents
  • B-Cell Activating Factor
  • epratuzumab
  • Rituximab