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Superior survival of ex vivo cultured human reticulocytes following transfusion into mice

The generation of cultured red blood cells from stem cell sources may fill an unmet clinical need for transfusion-dependent patients, particularly in countries that lack a sufficient and safe blood supply. Cultured red blood cells were generated from human CD34(+) cells from adult peripheral blood o...

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Autores principales: Kupzig, Sabine, Parsons, Stephen F., Curnow, Elinor, Anstee, David J., Blair, Allison
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394952/
https://www.ncbi.nlm.nih.gov/pubmed/27909219
http://dx.doi.org/10.3324/haematol.2016.154443
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author Kupzig, Sabine
Parsons, Stephen F.
Curnow, Elinor
Anstee, David J.
Blair, Allison
author_facet Kupzig, Sabine
Parsons, Stephen F.
Curnow, Elinor
Anstee, David J.
Blair, Allison
author_sort Kupzig, Sabine
collection PubMed
description The generation of cultured red blood cells from stem cell sources may fill an unmet clinical need for transfusion-dependent patients, particularly in countries that lack a sufficient and safe blood supply. Cultured red blood cells were generated from human CD34(+) cells from adult peripheral blood or cord blood by ex vivo expansion, and a comprehensive in vivo survival comparison with standard red cell concentrates was undertaken. Significant amplification (>10(5)-fold) was achieved using CD34(+) cells from both cord blood and peripheral blood, generating high yields of enucleated cultured red blood cells. Following transfusion, higher levels of cultured red cells could be detected in the murine circulation compared to standard adult red cells. The proportions of cultured blood cells from cord or peripheral blood sources remained high 24 hours post-transfusion (82±5% and 78±9%, respectively), while standard adult blood cells declined rapidly to only 49±9% by this time. In addition, the survival time of cultured blood cells in mice was longer than that of standard adult red cells. A paired comparison of cultured blood cells and standard adult red blood cells from the same donor confirmed the enhanced in vivo survival capacity of the cultured cells. The study herein represents the first demonstration that ex vivo generated cultured red blood cells survive longer than donor red cells using an in vivo model that more closely mimics clinical transfusion. Cultured red blood cells may offer advantages for transfusion-dependent patients by reducing the number of transfusions required.
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spelling pubmed-53949522017-06-21 Superior survival of ex vivo cultured human reticulocytes following transfusion into mice Kupzig, Sabine Parsons, Stephen F. Curnow, Elinor Anstee, David J. Blair, Allison Haematologica Articles The generation of cultured red blood cells from stem cell sources may fill an unmet clinical need for transfusion-dependent patients, particularly in countries that lack a sufficient and safe blood supply. Cultured red blood cells were generated from human CD34(+) cells from adult peripheral blood or cord blood by ex vivo expansion, and a comprehensive in vivo survival comparison with standard red cell concentrates was undertaken. Significant amplification (>10(5)-fold) was achieved using CD34(+) cells from both cord blood and peripheral blood, generating high yields of enucleated cultured red blood cells. Following transfusion, higher levels of cultured red cells could be detected in the murine circulation compared to standard adult red cells. The proportions of cultured blood cells from cord or peripheral blood sources remained high 24 hours post-transfusion (82±5% and 78±9%, respectively), while standard adult blood cells declined rapidly to only 49±9% by this time. In addition, the survival time of cultured blood cells in mice was longer than that of standard adult red cells. A paired comparison of cultured blood cells and standard adult red blood cells from the same donor confirmed the enhanced in vivo survival capacity of the cultured cells. The study herein represents the first demonstration that ex vivo generated cultured red blood cells survive longer than donor red cells using an in vivo model that more closely mimics clinical transfusion. Cultured red blood cells may offer advantages for transfusion-dependent patients by reducing the number of transfusions required. Ferrata Storti Foundation 2017-03 /pmc/articles/PMC5394952/ /pubmed/27909219 http://dx.doi.org/10.3324/haematol.2016.154443 Text en Copyright©2017 Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher.
spellingShingle Articles
Kupzig, Sabine
Parsons, Stephen F.
Curnow, Elinor
Anstee, David J.
Blair, Allison
Superior survival of ex vivo cultured human reticulocytes following transfusion into mice
title Superior survival of ex vivo cultured human reticulocytes following transfusion into mice
title_full Superior survival of ex vivo cultured human reticulocytes following transfusion into mice
title_fullStr Superior survival of ex vivo cultured human reticulocytes following transfusion into mice
title_full_unstemmed Superior survival of ex vivo cultured human reticulocytes following transfusion into mice
title_short Superior survival of ex vivo cultured human reticulocytes following transfusion into mice
title_sort superior survival of ex vivo cultured human reticulocytes following transfusion into mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394952/
https://www.ncbi.nlm.nih.gov/pubmed/27909219
http://dx.doi.org/10.3324/haematol.2016.154443
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