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CD4+ T cells in aged or thymectomized recipients of allogeneic stem cell transplantations

BACKGROUND: CD4+CD25highFOXP3+ regulatory T (Treg) cells, which include thymus-derived and peripherally induced cells, play a central role in immune regulation, and are therefore crucial to prevent graft-versus-host disease (GVHD). The increasing use of allogeneic hematopoietic stem cell transplanta...

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Autores principales: Takahashi, Hiroshi, Ikeda, Kazuhiko, Ogawa, Kazuei, Saito, Syunnichi, Ngoma, Alain M, Mashimo, Yumiko, Ueda, Koki, Furukawa, Miki, Shichishima-Nakamura, Akiko, Ohkawara, Hiroshi, Nollet, Kenneth E, Ohto, Hitoshi, Takeishi, Yasuchika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514962/
https://www.ncbi.nlm.nih.gov/pubmed/26210500
http://dx.doi.org/10.1186/s40659-015-0033-8
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author Takahashi, Hiroshi
Ikeda, Kazuhiko
Ogawa, Kazuei
Saito, Syunnichi
Ngoma, Alain M
Mashimo, Yumiko
Ueda, Koki
Furukawa, Miki
Shichishima-Nakamura, Akiko
Ohkawara, Hiroshi
Nollet, Kenneth E
Ohto, Hitoshi
Takeishi, Yasuchika
author_facet Takahashi, Hiroshi
Ikeda, Kazuhiko
Ogawa, Kazuei
Saito, Syunnichi
Ngoma, Alain M
Mashimo, Yumiko
Ueda, Koki
Furukawa, Miki
Shichishima-Nakamura, Akiko
Ohkawara, Hiroshi
Nollet, Kenneth E
Ohto, Hitoshi
Takeishi, Yasuchika
author_sort Takahashi, Hiroshi
collection PubMed
description BACKGROUND: CD4+CD25highFOXP3+ regulatory T (Treg) cells, which include thymus-derived and peripherally induced cells, play a central role in immune regulation, and are therefore crucial to prevent graft-versus-host disease (GVHD). The increasing use of allogeneic hematopoietic stem cell transplantation (allo-HSCT) for elderly patients with thymus regression, and our case of allo-HSCT shortly after total thymectomy, raised questions about the activity of thymus-derived Treg cells and peripherally induced Treg cells, which are otherwise indistinguishable. RESULTS: We found that despite pre-transplant thymectomy or older age, both naïve and effector Treg cells, as well as naïve and effector conventional T cells, proliferated in allo-HSCT recipients. Higher proportions of total Treg cells 1 month post allo-HSCT, and naïve Treg cells 1 year post allo-HSCT, appeared in patients achieving complete chimera without developing significant chronic GVHD, including our thymectomized patient, compared with patients who developed chronic GVHD. CONCLUSIONS: Treg cells that modulate human allogeneic immunity may arise peripherally as well as in the thymus of allo-HSCT recipients.
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spelling pubmed-45149622015-07-26 CD4+ T cells in aged or thymectomized recipients of allogeneic stem cell transplantations Takahashi, Hiroshi Ikeda, Kazuhiko Ogawa, Kazuei Saito, Syunnichi Ngoma, Alain M Mashimo, Yumiko Ueda, Koki Furukawa, Miki Shichishima-Nakamura, Akiko Ohkawara, Hiroshi Nollet, Kenneth E Ohto, Hitoshi Takeishi, Yasuchika Biol Res Research Article BACKGROUND: CD4+CD25highFOXP3+ regulatory T (Treg) cells, which include thymus-derived and peripherally induced cells, play a central role in immune regulation, and are therefore crucial to prevent graft-versus-host disease (GVHD). The increasing use of allogeneic hematopoietic stem cell transplantation (allo-HSCT) for elderly patients with thymus regression, and our case of allo-HSCT shortly after total thymectomy, raised questions about the activity of thymus-derived Treg cells and peripherally induced Treg cells, which are otherwise indistinguishable. RESULTS: We found that despite pre-transplant thymectomy or older age, both naïve and effector Treg cells, as well as naïve and effector conventional T cells, proliferated in allo-HSCT recipients. Higher proportions of total Treg cells 1 month post allo-HSCT, and naïve Treg cells 1 year post allo-HSCT, appeared in patients achieving complete chimera without developing significant chronic GVHD, including our thymectomized patient, compared with patients who developed chronic GVHD. CONCLUSIONS: Treg cells that modulate human allogeneic immunity may arise peripherally as well as in the thymus of allo-HSCT recipients. BioMed Central 2015-07-26 /pmc/articles/PMC4514962/ /pubmed/26210500 http://dx.doi.org/10.1186/s40659-015-0033-8 Text en © Takahashi et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Takahashi, Hiroshi
Ikeda, Kazuhiko
Ogawa, Kazuei
Saito, Syunnichi
Ngoma, Alain M
Mashimo, Yumiko
Ueda, Koki
Furukawa, Miki
Shichishima-Nakamura, Akiko
Ohkawara, Hiroshi
Nollet, Kenneth E
Ohto, Hitoshi
Takeishi, Yasuchika
CD4+ T cells in aged or thymectomized recipients of allogeneic stem cell transplantations
title CD4+ T cells in aged or thymectomized recipients of allogeneic stem cell transplantations
title_full CD4+ T cells in aged or thymectomized recipients of allogeneic stem cell transplantations
title_fullStr CD4+ T cells in aged or thymectomized recipients of allogeneic stem cell transplantations
title_full_unstemmed CD4+ T cells in aged or thymectomized recipients of allogeneic stem cell transplantations
title_short CD4+ T cells in aged or thymectomized recipients of allogeneic stem cell transplantations
title_sort cd4+ t cells in aged or thymectomized recipients of allogeneic stem cell transplantations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514962/
https://www.ncbi.nlm.nih.gov/pubmed/26210500
http://dx.doi.org/10.1186/s40659-015-0033-8
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