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Autologous hematopoietic stem cell transplantation for refractory antiphospholipid syndrome causing myocardial necrosis

Bone Marrow Transplantation volume 33, pages 863–866 (2004)Cite this article

Summary:

Autologous hematopoietic stem cell transplantation (HSCT) is currently being evaluated as a treatment for autoimmune diseases, including systemic lupus erythematosus (SLE), that are associated with a very severe prognosis. We describe a 27-year-old woman with SLE with a 10-year history of refractory antiphospholipid syndrome (APS). She developed progressive myocardial necrosis despite treatment with corticosteroids, cyclophosphamide (CYC), cyclosporine, and immunopheresis. After conditioning with CYC, fludarabine, and antithymocyte globulin, autologous HSCT using CD34+ selection was performed. After transplantation, the clinical symptoms caused by APS remitted, and the serum anticardiolipin antibody level decreased. Remission has persisted for 21 months after transplantation. Although a longer follow-up is required for the assessment of efficacy, autologous HSCT may cure patients with refractory APS.

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Acknowledgements

We acknowledge Dr S Nishiyama for providing the clinical data and the nursing staff of Hyogo College of Medicine for their assistance in autologous HSCT.

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Authors and Affiliations

  1. Division of Rheumatology and Clinical Immunology, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan

    N Hashimoto, T Iwasaki, M Sekiguchi & H Sano

  2. Division of Hematology and Oncology, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan

    H Takatsuka & T Okamoto

  3. Hashimoto Clinic for Rheumatic Diseases, Chuo-ku, Osaka, Japan

    T Hashimoto

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  1. N Hashimoto
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  2. T Iwasaki
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Correspondence to T Iwasaki.

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Hashimoto, N., Iwasaki, T., Sekiguchi, M. et al. Autologous hematopoietic stem cell transplantation for refractory antiphospholipid syndrome causing myocardial necrosis. Bone Marrow Transplant 33, 863–866 (2004). https://doi.org/10.1038/sj.bmt.1704432

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  • DOI: https://doi.org/10.1038/sj.bmt.1704432

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