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Individualization of Hematopoietic Stem Cell Transplantation Using Alpha/Beta T-Cell Depletion

Allogeneic hematopoietic stem cell transplantation (HSCT) is associated with several potentially lethal complications. Higher levels of CD3+ T-cells in the graft have been associated with increased risk of graft-versus-host disease (GVHD), but also beneficial graft-versus-leukemia effect and reduced...

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Autores principales: Rådestad, Emelie, Sundin, Mikael, Törlén, Johan, Thunberg, Sarah, Önfelt, Björn, Ljungman, Per, Watz, Emma, Mattsson, Jonas, Uhlin, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378311/
https://www.ncbi.nlm.nih.gov/pubmed/30804948
http://dx.doi.org/10.3389/fimmu.2019.00189
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author Rådestad, Emelie
Sundin, Mikael
Törlén, Johan
Thunberg, Sarah
Önfelt, Björn
Ljungman, Per
Watz, Emma
Mattsson, Jonas
Uhlin, Michael
author_facet Rådestad, Emelie
Sundin, Mikael
Törlén, Johan
Thunberg, Sarah
Önfelt, Björn
Ljungman, Per
Watz, Emma
Mattsson, Jonas
Uhlin, Michael
author_sort Rådestad, Emelie
collection PubMed
description Allogeneic hematopoietic stem cell transplantation (HSCT) is associated with several potentially lethal complications. Higher levels of CD3+ T-cells in the graft have been associated with increased risk of graft-versus-host disease (GVHD), but also beneficial graft-versus-leukemia effect and reduced infections. To tackle post-transplant complications, donor lymphocyte infusions have been used but with an increased risk of GVHD. To reduce this risk, we performed depletion of αβ T-cells and treated 12 patients post-HSCT suffering from infections and/or poor immune reconstitution. The αβ T-cell depleted cell products were characterized by flow cytometry. The median log depletion of αβ T-cells was −4.3 and the median yield of γδ T-cells was 73.5%. The median CD34+ cell dose was 4.4 × 10(6)/kg. All 12 patients were alive 3 months after infusion and after 1 year, two patients had died. No infusion-related side effects were reported and no severe acute GVHD (grade III-IV) developed in any patient post-infusion. Overall, 3 months after infusion 11 out of 12 patients had increased levels of platelets and/or granulocytes. In conclusion, we describe the use of αβ T-cell depleted products as stem cell boosters with encouraging results.
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spelling pubmed-63783112019-02-25 Individualization of Hematopoietic Stem Cell Transplantation Using Alpha/Beta T-Cell Depletion Rådestad, Emelie Sundin, Mikael Törlén, Johan Thunberg, Sarah Önfelt, Björn Ljungman, Per Watz, Emma Mattsson, Jonas Uhlin, Michael Front Immunol Immunology Allogeneic hematopoietic stem cell transplantation (HSCT) is associated with several potentially lethal complications. Higher levels of CD3+ T-cells in the graft have been associated with increased risk of graft-versus-host disease (GVHD), but also beneficial graft-versus-leukemia effect and reduced infections. To tackle post-transplant complications, donor lymphocyte infusions have been used but with an increased risk of GVHD. To reduce this risk, we performed depletion of αβ T-cells and treated 12 patients post-HSCT suffering from infections and/or poor immune reconstitution. The αβ T-cell depleted cell products were characterized by flow cytometry. The median log depletion of αβ T-cells was −4.3 and the median yield of γδ T-cells was 73.5%. The median CD34+ cell dose was 4.4 × 10(6)/kg. All 12 patients were alive 3 months after infusion and after 1 year, two patients had died. No infusion-related side effects were reported and no severe acute GVHD (grade III-IV) developed in any patient post-infusion. Overall, 3 months after infusion 11 out of 12 patients had increased levels of platelets and/or granulocytes. In conclusion, we describe the use of αβ T-cell depleted products as stem cell boosters with encouraging results. Frontiers Media S.A. 2019-02-11 /pmc/articles/PMC6378311/ /pubmed/30804948 http://dx.doi.org/10.3389/fimmu.2019.00189 Text en Copyright © 2019 Rådestad, Sundin, Törlén, Thunberg, Önfelt, Ljungman, Watz, Mattsson and Uhlin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Rådestad, Emelie
Sundin, Mikael
Törlén, Johan
Thunberg, Sarah
Önfelt, Björn
Ljungman, Per
Watz, Emma
Mattsson, Jonas
Uhlin, Michael
Individualization of Hematopoietic Stem Cell Transplantation Using Alpha/Beta T-Cell Depletion
title Individualization of Hematopoietic Stem Cell Transplantation Using Alpha/Beta T-Cell Depletion
title_full Individualization of Hematopoietic Stem Cell Transplantation Using Alpha/Beta T-Cell Depletion
title_fullStr Individualization of Hematopoietic Stem Cell Transplantation Using Alpha/Beta T-Cell Depletion
title_full_unstemmed Individualization of Hematopoietic Stem Cell Transplantation Using Alpha/Beta T-Cell Depletion
title_short Individualization of Hematopoietic Stem Cell Transplantation Using Alpha/Beta T-Cell Depletion
title_sort individualization of hematopoietic stem cell transplantation using alpha/beta t-cell depletion
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378311/
https://www.ncbi.nlm.nih.gov/pubmed/30804948
http://dx.doi.org/10.3389/fimmu.2019.00189
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