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Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients
To obtain a qualitative as well as quantitative view immune reconstitution following umbilical cord blood (UCB) transplantation of paediatric patients, we utilised a broad panel of flow cytometry markers to monitor the phenotypes of lymphoid and myeloid cells at 1‐12 months post‐transplant. Samples...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176140/ https://www.ncbi.nlm.nih.gov/pubmed/35847689 http://dx.doi.org/10.1002/jha2.12 |
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author | Girdlestone, John Raymond, Meera Shaw, Bronwen Tulpule, Sameer Devlia, Vikesh R. Danby, Robert Ahyee, Trudy Saudemont, Aurore Hough, Rachael Veys, Paul Ruggeri, Annalisa Vora, Ajay Marks, David I. Gibson, Brenda Wynn, Robert Madrigal, Alejandro Navarrete, Cristina V. |
author_facet | Girdlestone, John Raymond, Meera Shaw, Bronwen Tulpule, Sameer Devlia, Vikesh R. Danby, Robert Ahyee, Trudy Saudemont, Aurore Hough, Rachael Veys, Paul Ruggeri, Annalisa Vora, Ajay Marks, David I. Gibson, Brenda Wynn, Robert Madrigal, Alejandro Navarrete, Cristina V. |
author_sort | Girdlestone, John |
collection | PubMed |
description | To obtain a qualitative as well as quantitative view immune reconstitution following umbilical cord blood (UCB) transplantation of paediatric patients, we utilised a broad panel of flow cytometry markers to monitor the phenotypes of lymphoid and myeloid cells at 1‐12 months post‐transplant. Samples were received from 46 patients with a median age of 3.3 years and survival was 76% at 1 year. Monocytes were at similar or higher median levels than in adult controls at all times tested, with a high CD16+ proportion in the first 3 months. NK cells were also within adult ranges, with a CD56++ high proportion in the first 6 months. B cell recovery was seen from 2 months in most patients and T cells from 3 months, both were delayed with anti‐thymocyte globulin (ATG) treatment. CD4:CD8 ratios were high in the first 6 months, and the proportion of T cells with recent thymic emigrant and naïve phenotypes rose from 3 months. NK and plasmacytoid dendritic cell numbers remained at reduced levels in patients not surviving to 1 year. Our results can serve as a useful reference for detailed monitoring of immune reconstitution in paediatric recipients of UCB. |
format | Online Article Text |
id | pubmed-9176140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91761402022-07-14 Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients Girdlestone, John Raymond, Meera Shaw, Bronwen Tulpule, Sameer Devlia, Vikesh R. Danby, Robert Ahyee, Trudy Saudemont, Aurore Hough, Rachael Veys, Paul Ruggeri, Annalisa Vora, Ajay Marks, David I. Gibson, Brenda Wynn, Robert Madrigal, Alejandro Navarrete, Cristina V. EJHaem Cellular Therapy To obtain a qualitative as well as quantitative view immune reconstitution following umbilical cord blood (UCB) transplantation of paediatric patients, we utilised a broad panel of flow cytometry markers to monitor the phenotypes of lymphoid and myeloid cells at 1‐12 months post‐transplant. Samples were received from 46 patients with a median age of 3.3 years and survival was 76% at 1 year. Monocytes were at similar or higher median levels than in adult controls at all times tested, with a high CD16+ proportion in the first 3 months. NK cells were also within adult ranges, with a CD56++ high proportion in the first 6 months. B cell recovery was seen from 2 months in most patients and T cells from 3 months, both were delayed with anti‐thymocyte globulin (ATG) treatment. CD4:CD8 ratios were high in the first 6 months, and the proportion of T cells with recent thymic emigrant and naïve phenotypes rose from 3 months. NK and plasmacytoid dendritic cell numbers remained at reduced levels in patients not surviving to 1 year. Our results can serve as a useful reference for detailed monitoring of immune reconstitution in paediatric recipients of UCB. John Wiley and Sons Inc. 2020-05-21 /pmc/articles/PMC9176140/ /pubmed/35847689 http://dx.doi.org/10.1002/jha2.12 Text en © 2020 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cellular Therapy Girdlestone, John Raymond, Meera Shaw, Bronwen Tulpule, Sameer Devlia, Vikesh R. Danby, Robert Ahyee, Trudy Saudemont, Aurore Hough, Rachael Veys, Paul Ruggeri, Annalisa Vora, Ajay Marks, David I. Gibson, Brenda Wynn, Robert Madrigal, Alejandro Navarrete, Cristina V. Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients |
title | Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients |
title_full | Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients |
title_fullStr | Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients |
title_full_unstemmed | Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients |
title_short | Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients |
title_sort | immune reconstitution following umbilical cord blood transplantation: ires, a study of uk paediatric patients |
topic | Cellular Therapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176140/ https://www.ncbi.nlm.nih.gov/pubmed/35847689 http://dx.doi.org/10.1002/jha2.12 |
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