Clinical and immunological follow-up of pemphigus patients on adjuvant treatment with immunoadsorption or rituximab

Dermatology. 2009;218(3):237-45. doi: 10.1159/000187431. Epub 2008 Dec 16.

Abstract

Background: Pemphigus vulgaris (PV) is a life-threatening autoimmune blistering skin disease which is associated with pathogenic IgG autoantibodies against desmogleins (Dsg) 1 and 3. Novel therapeutic strategies such as immunoadsorption (IA) or the anti-CD20 antibody rituximab (Rtx) hold promise to be effective in severe or recalcitrant PV.

Patients and methods: In the present retrospective study, 6 patients with extensive cutaneous PV were subjected to adjuvant IA treatment while 5 patients with severe mucosal PV received adjuvant Rtx treatment.

Results: Within 6 months, IA and Rtx induced excellent clinical responses which were associated with a significant reduction of prednisolone doses and a decrease in anti-Dsg-specific IgG. Over a 12-month period, 3 IA-treated patients required additional adjuvant drugs while all of the PV patients on Rtx had no or only minimal residual symptoms.

Conclusion: The relative therapeutic (long-term) efficacy of IA and Rtx in cutaneous versus mucosal PV needs to be evaluated in a prospective study.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal / therapeutic use*
  • Antibodies, Monoclonal, Murine-Derived
  • Autoantibodies / blood
  • Desmoglein 1 / immunology
  • Desmoglein 3 / immunology
  • Female
  • Humans
  • Immunoglobulin G / immunology
  • Immunologic Factors / therapeutic use*
  • Immunosorbent Techniques*
  • Male
  • Middle Aged
  • Pemphigus / immunology
  • Pemphigus / pathology
  • Pemphigus / therapy*
  • Rituximab

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Autoantibodies
  • Desmoglein 1
  • Desmoglein 3
  • Immunoglobulin G
  • Immunologic Factors
  • Rituximab