Antigen-Specific Immunoadsorption With the Glycosorb® ABO Immunoadsorption System as a Novel Treatment Modality in Pure Red Cell Aplasia Following Major and Bidirectional ABO-Incompatible Allogeneic Hematopoietic Stem Cell Transplantation

Pure red cell aplasia (PRCA) after ABO-incompatible allogeneic hematopoietic stem cell transplantation (HSCT) is caused by persisting host-derived isohemagglutinins directed against donor red blood cell (RBC) antigens. ABO antigen-specific immunoadsorption (ABO-IA) with Glycosorb®, commonly used for...

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Main Authors: Ammon Handisurya, Nina Worel, Werner Rabitsch, Marija Bojic, Sahra Pajenda, Roman Reindl-Schwaighofer, Wolfgang Winnicki, Andreas Vychytil, Hanna A. Knaus, Rainer Oberbauer, Kurt Derfler, Philipp Wohlfarth
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-10-01
Series:Frontiers in Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2020.585628/full
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spelling doaj-38314e7bdc4b4128b4a7a5e8f12d04f12020-11-25T03:03:04ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2020-10-01710.3389/fmed.2020.585628585628Antigen-Specific Immunoadsorption With the Glycosorb® ABO Immunoadsorption System as a Novel Treatment Modality in Pure Red Cell Aplasia Following Major and Bidirectional ABO-Incompatible Allogeneic Hematopoietic Stem Cell TransplantationAmmon Handisurya0Ammon Handisurya1Nina Worel2Werner Rabitsch3Marija Bojic4Sahra Pajenda5Roman Reindl-Schwaighofer6Wolfgang Winnicki7Andreas Vychytil8Hanna A. Knaus9Rainer Oberbauer10Kurt Derfler11Philipp Wohlfarth12Department of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria1st Medical Department, Hanusch Hospital, Vienna, AustriaDepartment of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, Vienna, AustriaDepartment of Medicine I, Stem Cell Transplantation Unit, Medical University of Vienna, Vienna, AustriaDepartment of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, AustriaDepartment of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, AustriaDepartment of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, AustriaDepartment of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, AustriaDepartment of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, AustriaDepartment of Medicine I, Stem Cell Transplantation Unit, Medical University of Vienna, Vienna, AustriaDepartment of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, AustriaDepartment of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, AustriaDepartment of Medicine I, Stem Cell Transplantation Unit, Medical University of Vienna, Vienna, AustriaPure red cell aplasia (PRCA) after ABO-incompatible allogeneic hematopoietic stem cell transplantation (HSCT) is caused by persisting host-derived isohemagglutinins directed against donor red blood cell (RBC) antigens. ABO antigen-specific immunoadsorption (ABO-IA) with Glycosorb®, commonly used for desensitization therapy in ABO-incompatible living donor renal transplantation, specifically eliminates circulating isohemagglutinins and might represent a novel treatment option for post-HSCT PRCA. In this prospective observational (n = 3) and retrospective (n = 3) analysis of six adult HSCT-recipients with PRCA, ABO-IA was initiated at 159 (range: 104–186) days following HSCT. The median treatment frequency was 4.5 (range: 3.9–5.5) sessions/week. ABO-IA-treatment led to a continuous decrease in isohemagglutinin titers. Reticulocytes increased to ≥30 G/L after 17.5 (range: 4–37) immunoadsorption sessions over 28.5 (range: 6–49) days and continued to rise after that. By the end of the 3-month follow-up period after discontinuation of ABO-IA, all patients showed a sustained remission of PRCA and were independent of erythropoietin-stimulating agents and transfusions. No case of infection or graft-versus-host disease was observed. After a median follow-up of 22.03 (range: 6.08–149.00) months after ABO-IA-treatment, all patients were alive and showed a stable RBC engraftment of the donor blood group. Our data provide the first evidence for ABO-IA as an effective treatment for post-HSCT PRCA.https://www.frontiersin.org/articles/10.3389/fmed.2020.585628/fullpure red blood cell aplasia (PRCA)immunoadsorptionhematopoeietic stem cell transplantationisohemagglutininsGlycosorb®
collection DOAJ
language English
format Article
sources DOAJ
author Ammon Handisurya
Ammon Handisurya
Nina Worel
Werner Rabitsch
Marija Bojic
Sahra Pajenda
Roman Reindl-Schwaighofer
Wolfgang Winnicki
Andreas Vychytil
Hanna A. Knaus
Rainer Oberbauer
Kurt Derfler
Philipp Wohlfarth
spellingShingle Ammon Handisurya
Ammon Handisurya
Nina Worel
Werner Rabitsch
Marija Bojic
Sahra Pajenda
Roman Reindl-Schwaighofer
Wolfgang Winnicki
Andreas Vychytil
Hanna A. Knaus
Rainer Oberbauer
Kurt Derfler
Philipp Wohlfarth
Antigen-Specific Immunoadsorption With the Glycosorb® ABO Immunoadsorption System as a Novel Treatment Modality in Pure Red Cell Aplasia Following Major and Bidirectional ABO-Incompatible Allogeneic Hematopoietic Stem Cell Transplantation
Frontiers in Medicine
pure red blood cell aplasia (PRCA)
immunoadsorption
hematopoeietic stem cell transplantation
isohemagglutinins
Glycosorb®
author_facet Ammon Handisurya
Ammon Handisurya
Nina Worel
Werner Rabitsch
Marija Bojic
Sahra Pajenda
Roman Reindl-Schwaighofer
Wolfgang Winnicki
Andreas Vychytil
Hanna A. Knaus
Rainer Oberbauer
Kurt Derfler
Philipp Wohlfarth
author_sort Ammon Handisurya
title Antigen-Specific Immunoadsorption With the Glycosorb® ABO Immunoadsorption System as a Novel Treatment Modality in Pure Red Cell Aplasia Following Major and Bidirectional ABO-Incompatible Allogeneic Hematopoietic Stem Cell Transplantation
title_short Antigen-Specific Immunoadsorption With the Glycosorb® ABO Immunoadsorption System as a Novel Treatment Modality in Pure Red Cell Aplasia Following Major and Bidirectional ABO-Incompatible Allogeneic Hematopoietic Stem Cell Transplantation
title_full Antigen-Specific Immunoadsorption With the Glycosorb® ABO Immunoadsorption System as a Novel Treatment Modality in Pure Red Cell Aplasia Following Major and Bidirectional ABO-Incompatible Allogeneic Hematopoietic Stem Cell Transplantation
title_fullStr Antigen-Specific Immunoadsorption With the Glycosorb® ABO Immunoadsorption System as a Novel Treatment Modality in Pure Red Cell Aplasia Following Major and Bidirectional ABO-Incompatible Allogeneic Hematopoietic Stem Cell Transplantation
title_full_unstemmed Antigen-Specific Immunoadsorption With the Glycosorb® ABO Immunoadsorption System as a Novel Treatment Modality in Pure Red Cell Aplasia Following Major and Bidirectional ABO-Incompatible Allogeneic Hematopoietic Stem Cell Transplantation
title_sort antigen-specific immunoadsorption with the glycosorb® abo immunoadsorption system as a novel treatment modality in pure red cell aplasia following major and bidirectional abo-incompatible allogeneic hematopoietic stem cell transplantation
publisher Frontiers Media S.A.
series Frontiers in Medicine
issn 2296-858X
publishDate 2020-10-01
description Pure red cell aplasia (PRCA) after ABO-incompatible allogeneic hematopoietic stem cell transplantation (HSCT) is caused by persisting host-derived isohemagglutinins directed against donor red blood cell (RBC) antigens. ABO antigen-specific immunoadsorption (ABO-IA) with Glycosorb®, commonly used for desensitization therapy in ABO-incompatible living donor renal transplantation, specifically eliminates circulating isohemagglutinins and might represent a novel treatment option for post-HSCT PRCA. In this prospective observational (n = 3) and retrospective (n = 3) analysis of six adult HSCT-recipients with PRCA, ABO-IA was initiated at 159 (range: 104–186) days following HSCT. The median treatment frequency was 4.5 (range: 3.9–5.5) sessions/week. ABO-IA-treatment led to a continuous decrease in isohemagglutinin titers. Reticulocytes increased to ≥30 G/L after 17.5 (range: 4–37) immunoadsorption sessions over 28.5 (range: 6–49) days and continued to rise after that. By the end of the 3-month follow-up period after discontinuation of ABO-IA, all patients showed a sustained remission of PRCA and were independent of erythropoietin-stimulating agents and transfusions. No case of infection or graft-versus-host disease was observed. After a median follow-up of 22.03 (range: 6.08–149.00) months after ABO-IA-treatment, all patients were alive and showed a stable RBC engraftment of the donor blood group. Our data provide the first evidence for ABO-IA as an effective treatment for post-HSCT PRCA.
topic pure red blood cell aplasia (PRCA)
immunoadsorption
hematopoeietic stem cell transplantation
isohemagglutinins
Glycosorb®
url https://www.frontiersin.org/articles/10.3389/fmed.2020.585628/full
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