Rituximab therapy in autoimmune pulmonary alveolar proteinosis

Eur Respir J. 2009 Jun;33(6):1503-6. doi: 10.1183/09031936.00160908.

Abstract

Idiopathic pulmonary alveolar proteinosis is presumed to be an autoimmune disorder that may lead to pulmonary insufficiency. However, steroids do not appear to be effective and the standard of therapy is whole-lung lavage. We report the first case of successful therapy with rituximab, which addresses the pathogenic mechanism of pulmonary alveolar proteinosis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antibodies, Monoclonal / therapeutic use*
  • Antibodies, Monoclonal, Murine-Derived
  • Autoimmune Diseases / diagnosis
  • Autoimmune Diseases / drug therapy*
  • Biopsy
  • Bronchoalveolar Lavage
  • Diagnosis, Differential
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Immunologic Factors / therapeutic use*
  • Pulmonary Alveolar Proteinosis / diagnosis
  • Pulmonary Alveolar Proteinosis / drug therapy*
  • Respiratory Function Tests
  • Rituximab
  • Tomography, X-Ray Computed

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Immunologic Factors
  • Rituximab