B cell suppression in primary glomerular disease

Adv Chronic Kidney Dis. 2014 Mar;21(2):166-81. doi: 10.1053/j.ackd.2014.01.005.

Abstract

Membranous nephropathy, focal segmental glomerulosclerosis (FSGS), and minimal change disease (MCD) are the most common causes of idiopathic nephrotic syndrome. For many years prednisone, alkylating agents, and calcineurin inhibitors have been the standard of therapy for these patients. More effective or better tolerated treatment modalities are needed. B cell targeted therapy was recently introduced in clinical practice. In this review, we briefly summarize the current standard therapy and discuss the efficacy of B cell targeted therapy in primary glomerular diseases. Observational, short-term studies suggest that rituximab is effective and comparable to standard therapy in maintaining remissions in patients with frequently relapsing or steroid-dependent MCD or FSGS. In contrast, response is limited in patients with steroid-resistant nephrotic syndrome. Rituximab also induces remissions in patients with membranous nephropathy. Controlled clinical trials on kidney endpoints are urgently needed to position B cell targeted therapy in clinical practice.

Keywords: Focal segmental glomerulosclerosis; Membranous nephropathy; Minimal change disease; Rituximab.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Abatacept
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Antibodies, Monoclonal, Murine-Derived / therapeutic use
  • B-Lymphocytes / immunology*
  • Glomerulonephritis / drug therapy
  • Glomerulonephritis / immunology
  • Glomerulonephritis, Membranous / drug therapy*
  • Glomerulonephritis, Membranous / immunology
  • Glomerulosclerosis, Focal Segmental / drug therapy*
  • Glomerulosclerosis, Focal Segmental / immunology
  • Humans
  • Immunoconjugates / therapeutic use
  • Immunosuppressive Agents / therapeutic use*
  • Nephrosis, Lipoid / drug therapy*
  • Nephrosis, Lipoid / immunology
  • Oligonucleotides / therapeutic use
  • Prednisone / therapeutic use
  • Recombinant Fusion Proteins / therapeutic use
  • Rituximab

Substances

  • Antibodies, Monoclonal, Humanized
  • Antibodies, Monoclonal, Murine-Derived
  • Immunoconjugates
  • Immunosuppressive Agents
  • Oligonucleotides
  • Recombinant Fusion Proteins
  • epratuzumab
  • Rituximab
  • belimumab
  • Abatacept
  • ocrelizumab
  • TACI receptor-IgG Fc fragment fusion protein
  • abetimus
  • Prednisone