Intensive immunosuppression and autologous stem cell transplantation for patients with severe rheumatoid arthritis: the Leiden experience

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Ten patients with active, destructive rheumatoid arthritis refractory to antirheumatic therapy enrolled in a study to evaluate the effects of intensive immunosuppression followed by autologous stem cell transplantation. Intensive immunosuppression was achieved with high dose cyclophosphamide as part of the mobilization (4 g/m2) and conditioning (200 mg/kg) regimen. The autologous stem cell products were enriched for CD34+ cells to minimize the chance of reinfusing autoreactive lymphocytes. Eight patients completed all consecutive treatment steps, one patient withdrew after mobilization because of improvement, one patient was taken off study because of pulmonary embolism. The treatment appeared feasible and safe, and marked sustained clinical improvement was observed in 6 patients, 2 of whom were previously unresponsive to tumor necrosis factor blocking therapy. In 5 patients disease modifying antirheumatic drugs were successfully withdrawn after transplantation. The treatment induced significant lymphopenia, with low levels of naive CD4+ T cells in particular, without clinical sequelae. Titers of rheumatoid factor dropped but did not normalize.

Original languageEnglish
Pages (from-to)25-7
Number of pages3
JournalScandinavian journal of rheumatology. Supplement
Volume64
Publication statusPublished - 2001

Keywords

  • Adult
  • Arthritis, Rheumatoid
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes
  • Combined Modality Therapy
  • Cyclophosphamide
  • Female
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Immunocompromised Host
  • Immunosuppressive Agents
  • Leukapheresis
  • Male
  • Middle Aged
  • Netherlands
  • Transplantation Conditioning
  • Transplantation, Autologous
  • Treatment Outcome
  • Clinical Trial
  • Clinical Trial, Phase I
  • Clinical Trial, Phase II
  • Journal Article
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

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