Immunoadsorption and autologous transplantation for life-threatening primary antiphospholipid syndrome

Author:

Angelillo-Scherrer Anne12ORCID,Mansouri Taleghani Behrouz1,Förger Frauke3,Baerlocher Gabriela M.12,Pabst Thomas4,Pöllinger Alexander5,Banz Yara6,Geiser Thomas7,Kremer Hovinga Johanna A.12ORCID,Rovó Alicia1

Affiliation:

1. Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital,

2. Department for BioMedical Research,

3. Department of Rheumatology, Immunology, Allergology, Inselspital, Bern University Hospital,

4. Department of Medical Oncology, Inselspital, Bern University Hospital,

5. Department of Diagnostic, Interventional and Pediatrics Radiology, Bern University Hospital,

6. Institute of Pathology, and

7. Department of Pulmonary Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland

Abstract

Key Points Reduction of APL antibodies by immunoadsorption may be a lifesaving therapy for the management of DAH with high titer of APL antibodies. Autologous HSCT may be a valid treatment option in patients with primary APS and no response to standard immunosuppressive therapy.

Publisher

American Society of Hematology

Subject

Hematology

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