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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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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. |
format | Online Article Text |
id | pubmed-6378311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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