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Correlation Between Stem and Progenitor Cells Number and Immune Response in Patients After Allogeneic Kidney Transplant
BACKGROUND: Stem and progenitor cells are of great interest in all medical procedures involving tissue regeneration. There is a consensus that the use of stem cells after solid organ transplantation may play a role in tissue repair and in immunosuppression. The aim of this study was to determine pos...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319141/ https://www.ncbi.nlm.nih.gov/pubmed/30573723 http://dx.doi.org/10.12659/AOT.912686 |
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author | Sieńko, Jerzy Kotowski, Maciej Paczkowska, Edyta Sobuś, Anna Tejchman, Karol Piątek, Jarosław Pilichowska, Ewa Kędzierska-Kapuza, Karolina Ostrowski, Marek |
author_facet | Sieńko, Jerzy Kotowski, Maciej Paczkowska, Edyta Sobuś, Anna Tejchman, Karol Piątek, Jarosław Pilichowska, Ewa Kędzierska-Kapuza, Karolina Ostrowski, Marek |
author_sort | Sieńko, Jerzy |
collection | PubMed |
description | BACKGROUND: Stem and progenitor cells are of great interest in all medical procedures involving tissue regeneration. There is a consensus that the use of stem cells after solid organ transplantation may play a role in tissue repair and in immunosuppression. The aim of this study was to determine possible relations between stem cell count and the immune response in a group of patients after kidney transplantation. MATERIAL/METHODS: The study was conducted on a group of 100 patients who underwent kidney transplantation. The following phenotypic markers of the studied cell subpopulations were adopted: T(reg) cells (CD3(+)CD4(+)CD25(high)), circulating hematopoietic cells (CD34(+)CD133(+)CD45(+)CD38(−)), and non-hematopoietic cells (Lin(−)CXCR4(+)CD133(−)CD45(−)). Cell subpopulations were assessed using LSRII flow cytometer (BD Biosciences, San Jose, CA, USA). RESULTS: Positive correlation was observed between non-hematopoietic stem cells percentage and recipient’s platelets count (P=0.04). Moreover, a higher percentage of non-hematopoietic cells was accompanied by lower numbers of B lymphocytes (P=0.03) and T(reg) cells (P=0.02). CONCLUSIONS: Our study revealed significant associations between the intensity of ongoing immune response processes and tissue damage, and the release of stem and progenitor cells into circulation. These findings suggest their role in the stimulation of protective processes in terms of graft regeneration. |
format | Online Article Text |
id | pubmed-6319141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63191412019-01-24 Correlation Between Stem and Progenitor Cells Number and Immune Response in Patients After Allogeneic Kidney Transplant Sieńko, Jerzy Kotowski, Maciej Paczkowska, Edyta Sobuś, Anna Tejchman, Karol Piątek, Jarosław Pilichowska, Ewa Kędzierska-Kapuza, Karolina Ostrowski, Marek Ann Transplant Original Paper BACKGROUND: Stem and progenitor cells are of great interest in all medical procedures involving tissue regeneration. There is a consensus that the use of stem cells after solid organ transplantation may play a role in tissue repair and in immunosuppression. The aim of this study was to determine possible relations between stem cell count and the immune response in a group of patients after kidney transplantation. MATERIAL/METHODS: The study was conducted on a group of 100 patients who underwent kidney transplantation. The following phenotypic markers of the studied cell subpopulations were adopted: T(reg) cells (CD3(+)CD4(+)CD25(high)), circulating hematopoietic cells (CD34(+)CD133(+)CD45(+)CD38(−)), and non-hematopoietic cells (Lin(−)CXCR4(+)CD133(−)CD45(−)). Cell subpopulations were assessed using LSRII flow cytometer (BD Biosciences, San Jose, CA, USA). RESULTS: Positive correlation was observed between non-hematopoietic stem cells percentage and recipient’s platelets count (P=0.04). Moreover, a higher percentage of non-hematopoietic cells was accompanied by lower numbers of B lymphocytes (P=0.03) and T(reg) cells (P=0.02). CONCLUSIONS: Our study revealed significant associations between the intensity of ongoing immune response processes and tissue damage, and the release of stem and progenitor cells into circulation. These findings suggest their role in the stimulation of protective processes in terms of graft regeneration. International Scientific Literature, Inc. 2018-12-21 /pmc/articles/PMC6319141/ /pubmed/30573723 http://dx.doi.org/10.12659/AOT.912686 Text en © Ann Transplant, 2018 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Original Paper Sieńko, Jerzy Kotowski, Maciej Paczkowska, Edyta Sobuś, Anna Tejchman, Karol Piątek, Jarosław Pilichowska, Ewa Kędzierska-Kapuza, Karolina Ostrowski, Marek Correlation Between Stem and Progenitor Cells Number and Immune Response in Patients After Allogeneic Kidney Transplant |
title | Correlation Between Stem and Progenitor Cells Number and Immune Response in Patients After Allogeneic Kidney Transplant |
title_full | Correlation Between Stem and Progenitor Cells Number and Immune Response in Patients After Allogeneic Kidney Transplant |
title_fullStr | Correlation Between Stem and Progenitor Cells Number and Immune Response in Patients After Allogeneic Kidney Transplant |
title_full_unstemmed | Correlation Between Stem and Progenitor Cells Number and Immune Response in Patients After Allogeneic Kidney Transplant |
title_short | Correlation Between Stem and Progenitor Cells Number and Immune Response in Patients After Allogeneic Kidney Transplant |
title_sort | correlation between stem and progenitor cells number and immune response in patients after allogeneic kidney transplant |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319141/ https://www.ncbi.nlm.nih.gov/pubmed/30573723 http://dx.doi.org/10.12659/AOT.912686 |
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