Long-term outcome of anti-glomerular basement membrane antibody disease treated with immunoadsorption

PLoS One. 2014 Jul 31;9(7):e103568. doi: 10.1371/journal.pone.0103568. eCollection 2014.

Abstract

Background: Anti-glomerular basement membrane (GBM) antibody disease may lead to acute crescentic glomerulonephritis with poor renal prognosis. Current therapy favours plasma exchange (PE) for removal of pathogenic antibodies. Immunoadsorption (IAS) is superior to PE regarding efficiency of antibody-removal and safety. Apart from anecdotal data, there is no systemic analysis of the long-term effects of IAS on anti-GBM-disease and antibody kinetics.

Objective: To examine the long-term effect of high-frequency IAS combined with standard immunosuppression on patient and renal survival in patients with anti-GBM-disease and to quantify antibody removal and kinetics through IAS.

Design: Retrospective review of patients treated with IAS for anti-GBM-antibody disease confirmed by biopsy and/or anti-GBM-antibodies.

Setting: University Hospital of Vienna, Austria.

Participants: 10 patients with anti-GBM-disease treated with IAS.

Measurements: Patient and renal survival, renal histology, anti-GBM-antibodies.

Results: Anti-GBM-antibodies were reduced by the first 9 IAS treatments (mean number of 23) to negative levels in all patients. Renal survival was 40% at diagnosis, 70% after the end of IAS, 63% after one year and 50% at the end of observation (mean 84 months, range 9 to 186). Dialysis dependency was successfully reversed in three of six patients. Patient survival was 90% at the end of observation.

Conclusion: IAS efficiently eliminates anti-GBM-antibodies suggesting non-inferiority to PE with regard to renal and patient survival. Hence IAS should be considered as a valuable treatment option for anti-GBM-disease, especially in patients presenting with a high percentage of crescents and dialysis dependency due to an unusual high proportion of responders.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anti-Glomerular Basement Membrane Disease / therapy*
  • Autoantibodies / blood
  • Autoantibodies / isolation & purification
  • Female
  • Humans
  • Male
  • Plasmapheresis*
  • Young Adult

Substances

  • Autoantibodies
  • antiglomerular basement membrane antibody

Grants and funding

The authors have no support or funding to report.