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Immunoadsorption and autologous transplantation for life-threatening primary antiphospholipid syndrome

Identifieur interne : 000270 ( Pmc/Curation ); précédent : 000269; suivant : 000271

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

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PMC:6737408

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Anne Angelillo-Scherrer
<affiliation>
<nlm:aff id="aff1">Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
</affiliation>
<affiliation>
<nlm:aff id="aff2">Department for BioMedical Research,</nlm:aff>
</affiliation>
Behrouz Mansouri Taleghani
<affiliation>
<nlm:aff id="aff1">Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
</affiliation>
Frauke Förger
<affiliation>
<nlm:aff id="aff3">Department of Rheumatology, Immunology, Allergology, Inselspital, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
</affiliation>
Gabriela M. Baerlocher
<affiliation>
<nlm:aff id="aff1">Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
</affiliation>
<affiliation>
<nlm:aff id="aff2">Department for BioMedical Research,</nlm:aff>
</affiliation>
Thomas Pabst
<affiliation>
<nlm:aff id="aff4">Department of Medical Oncology, Inselspital, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
</affiliation>
Alexander Pöllinger
<affiliation>
<nlm:aff id="aff5">Department of Diagnostic, Interventional and Pediatrics Radiology, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
</affiliation>
Johanna A. Kremer Hovinga
<affiliation>
<nlm:aff id="aff1">Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
</affiliation>
<affiliation>
<nlm:aff id="aff2">Department for BioMedical Research,</nlm:aff>
</affiliation>
Alicia Rov
<affiliation>
<nlm:aff id="aff1">Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
</affiliation>

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<nlm:aff id="aff1">Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital,</nlm:aff>
<wicri:noCountry code="subfield">Bern University Hospital</wicri:noCountry>
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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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<p>Autologous HSCT may be a valid treatment option in patients with primary APS and no response to standard immunosuppressive therapy.</p>
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</p>
</div>
</front>
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<journal-id journal-id-type="nlm-ta">Blood Adv</journal-id>
<journal-id journal-id-type="iso-abbrev">Blood Adv</journal-id>
<journal-id journal-id-type="hwp">bloodoa</journal-id>
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<subject>Exceptional Case Report</subject>
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<article-title>Immunoadsorption and autologous transplantation for life-threatening primary antiphospholipid syndrome</article-title>
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<surname>Mansouri Taleghani</surname>
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<name>
<surname>Banz</surname>
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</name>
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<contrib contrib-type="author">
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<name>
<surname>Kremer Hovinga</surname>
<given-names>Johanna A.</given-names>
</name>
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<xref ref-type="aff" rid="aff2">2</xref>
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<contrib contrib-type="author">
<name>
<surname>Rovó</surname>
<given-names>Alicia</given-names>
</name>
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Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital,</aff>
<aff id="aff2">
<label>2</label>
Department for BioMedical Research,</aff>
<aff id="aff3">
<label>3</label>
Department of Rheumatology, Immunology, Allergology, Inselspital, Bern University Hospital,</aff>
<aff id="aff4">
<label>4</label>
Department of Medical Oncology, Inselspital, Bern University Hospital,</aff>
<aff id="aff5">
<label>5</label>
Department of Diagnostic, Interventional and Pediatrics Radiology, Bern University Hospital,</aff>
<aff id="aff6">
<label>6</label>
Institute of Pathology, and</aff>
<aff id="aff7">
<label>7</label>
Department of Pulmonary Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland</aff>
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<month>9</month>
<year>2019</year>
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<month>9</month>
<year>2019</year>
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<volume>3</volume>
<issue>17</issue>
<fpage>2664</fpage>
<lpage>2667</lpage>
<history>
<date date-type="received">
<day>19</day>
<month>5</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>23</day>
<month>7</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>© 2019 by The American Society of Hematology</copyright-statement>
<copyright-year>2019</copyright-year>
<ali:free_to_read></ali:free_to_read>
</permissions>
<self-uri xlink:title="pdf" xlink:href="advancesADV2019000465.pdf"></self-uri>
<abstract abstract-type="executive-summary">
<title>Key Points</title>
<p>
<list list-type="bullet">
<list-item>
<p>Reduction of APL antibodies by immunoadsorption may be a lifesaving therapy for the management of DAH with high titer of APL antibodies.</p>
</list-item>
<list-item>
<p>Autologous HSCT may be a valid treatment option in patients with primary APS and no response to standard immunosuppressive therapy.</p>
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