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Immunoadsorption and autologous transplantation for life-threatening primary antiphospholipid syndrome

Identifieur interne : 000751 ( Main/Exploration ); précédent : 000750; suivant : 000752

Immunoadsorption and autologous transplantation for life-threatening primary antiphospholipid syndrome

Auteurs : Anne Angelillo-Scherrer ; Behrouz Mansouri Taleghani ; Frauke Förger ; Gabriela M. Baerlocher ; Thomas Pabst ; Alexander Pöllinger ; Yara Banz ; Thomas Geiser [Suisse] ; Johanna A. Kremer Hovinga ; Alicia Rov

Source :

RBID : PMC:6737408

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.


Url:
DOI: 10.1182/bloodadvances.2019000465
PubMed: 31506284
PubMed Central: 6737408


Affiliations:


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<p>Reduction of APL antibodies by immunoadsorption may be a lifesaving therapy for the management of DAH with high titer of APL antibodies.</p>
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