Rituximab treatment of the anti-synthetase syndrome: a retrospective case series

Rheumatology (Oxford). 2009 Aug;48(8):968-71. doi: 10.1093/rheumatology/kep157. Epub 2009 Jun 16.

Abstract

Objective: Interstitial lung disease (ILD) is the major determinant of morbidity and mortality in the anti-synthetase syndrome (ASS). Here we have retrospectively assessed 11 ASS patients with ILD treated with the anti-CD20 mAB rituximab at our tertiary referral hospital.

Methods: Data on clinical and laboratory parameters, lung imaging by high-resolution CT thorax and pulmonary function tests were collected from patient examinations done up to 6 months before rituximab was initiated, and at 3 and 6 months post-treatment.

Results: All the 11 ASS patients had severe and progressive ILD and most of them had previously failed on cyclophosphamide and/or other immuno-modulating agents. Rituximab appeared to stabilize and/or improve the ILD in 7 of 11 ASS patients during the first 6 months after treatment. The rituximab treatment appeared to decrease the serum level of anti-Jo-1 antibodies, but the decrease was most often modest. One patient developed a fatal infection 3 months after the last infusion with rituximab. In the other ASS patients, the treatment was well tolerated.

Conclusions: This retrospective case series indicates a short-term beneficial effect of rituximab in ASS. Prospective, controlled studies are needed to validate this finding and further assess safety issues.

MeSH terms

  • Antibodies, Antinuclear / immunology*
  • Antibodies, Monoclonal / therapeutic use*
  • Antibodies, Monoclonal, Murine-Derived
  • Antirheumatic Agents / therapeutic use*
  • Creatine Kinase / blood
  • Female
  • Humans
  • Lung Diseases, Interstitial / drug therapy*
  • Male
  • Middle Aged
  • Polymyositis / drug therapy*
  • Respiratory Function Tests
  • Retrospective Studies
  • Rituximab
  • Syndrome
  • Treatment Outcome

Substances

  • Antibodies, Antinuclear
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Antirheumatic Agents
  • Jo-1 antibody
  • Rituximab
  • Creatine Kinase