Differences of Clonogenic Mesenchymal Stem Cells on Immunomodulation of Lymphocyte Subsets

Mesenchymal stem cells (MSC) are a widely used population in cell therapy for their ability to differentiate into distinct tissues and more lately, for their immunomodulatory properties. However, the use of heterogeneous populations could be responsible for the nondesired outcomes reflected in the l...

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Main Authors: Pascual Martínez-Peinado, Sandra Pascual-García, Enrique Roche, José Miguel Sempere-Ortells
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2018/7232717
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author Pascual Martínez-Peinado
Sandra Pascual-García
Enrique Roche
José Miguel Sempere-Ortells
author_facet Pascual Martínez-Peinado
Sandra Pascual-García
Enrique Roche
José Miguel Sempere-Ortells
author_sort Pascual Martínez-Peinado
collection DOAJ
description Mesenchymal stem cells (MSC) are a widely used population in cell therapy for their ability to differentiate into distinct tissues and more lately, for their immunomodulatory properties. However, the use of heterogeneous populations could be responsible for the nondesired outcomes reflected in the literature. Here, we analyse the different capacities of five one-cell-derived MSC clones to exert their immunomodulation ex vivo. We assessed proliferation assays in cocultures of MSC clones and purified cluster of differentiation (CD)3+, CD4+, or CD8+ lymphocytes; analysed the regulatory T (Treg) cells fold change rate; determined the effects on viability of peripheral blood mononuclear cells (PBMC); and also measured the coculture cytokine profiles (Th1/Th2). Conditioned media (CM) of different clones were also used to perform both proliferation assays and to analyse Treg fold change. The five clones analysed in this work were able to generate heterogeneous environments. Different clones inhibited proliferation of CD3+ and CD4+ lymphocytes, with different intensities. Surprisingly, all clones promoted proliferation of CD8+ lymphocytes. Different MSC clones and their CM were able to increase the number of Treg with different intensities. Finally, different clones also promoted different effects on the viability of PBMC treated with ultraviolet light. Considering all these data together, it seems that different clones, even from the same donor, can promote a wide spectrum of responses from anti-inflammatory to proinflammatory character. This fact may be important to standardise the design of personalized cell therapy protocols, thus diminishing the aforementioned undesired outcomes existing nowadays in this type of therapies.
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spelling doaj-art-e3e4e2ab778c4c158372c8333bab419f2025-08-20T03:26:33ZengWileyJournal of Immunology Research2314-88612314-71562018-01-01201810.1155/2018/72327177232717Differences of Clonogenic Mesenchymal Stem Cells on Immunomodulation of Lymphocyte SubsetsPascual Martínez-Peinado0Sandra Pascual-García1Enrique Roche2José Miguel Sempere-Ortells3Immunology Division, Biotechnology Department, University of Alicante, San Vicente del Raspeig, Alicante, SpainImmunology Division, Biotechnology Department, University of Alicante, San Vicente del Raspeig, Alicante, SpainBiochemistry and Cell Therapy Unit, Institute of Bioengineering, University Miguel Hernandez, Elche, Alicante, SpainImmunology Division, Biotechnology Department, University of Alicante, San Vicente del Raspeig, Alicante, SpainMesenchymal stem cells (MSC) are a widely used population in cell therapy for their ability to differentiate into distinct tissues and more lately, for their immunomodulatory properties. However, the use of heterogeneous populations could be responsible for the nondesired outcomes reflected in the literature. Here, we analyse the different capacities of five one-cell-derived MSC clones to exert their immunomodulation ex vivo. We assessed proliferation assays in cocultures of MSC clones and purified cluster of differentiation (CD)3+, CD4+, or CD8+ lymphocytes; analysed the regulatory T (Treg) cells fold change rate; determined the effects on viability of peripheral blood mononuclear cells (PBMC); and also measured the coculture cytokine profiles (Th1/Th2). Conditioned media (CM) of different clones were also used to perform both proliferation assays and to analyse Treg fold change. The five clones analysed in this work were able to generate heterogeneous environments. Different clones inhibited proliferation of CD3+ and CD4+ lymphocytes, with different intensities. Surprisingly, all clones promoted proliferation of CD8+ lymphocytes. Different MSC clones and their CM were able to increase the number of Treg with different intensities. Finally, different clones also promoted different effects on the viability of PBMC treated with ultraviolet light. Considering all these data together, it seems that different clones, even from the same donor, can promote a wide spectrum of responses from anti-inflammatory to proinflammatory character. This fact may be important to standardise the design of personalized cell therapy protocols, thus diminishing the aforementioned undesired outcomes existing nowadays in this type of therapies.http://dx.doi.org/10.1155/2018/7232717
spellingShingle Pascual Martínez-Peinado
Sandra Pascual-García
Enrique Roche
José Miguel Sempere-Ortells
Differences of Clonogenic Mesenchymal Stem Cells on Immunomodulation of Lymphocyte Subsets
Journal of Immunology Research
title Differences of Clonogenic Mesenchymal Stem Cells on Immunomodulation of Lymphocyte Subsets
title_full Differences of Clonogenic Mesenchymal Stem Cells on Immunomodulation of Lymphocyte Subsets
title_fullStr Differences of Clonogenic Mesenchymal Stem Cells on Immunomodulation of Lymphocyte Subsets
title_full_unstemmed Differences of Clonogenic Mesenchymal Stem Cells on Immunomodulation of Lymphocyte Subsets
title_short Differences of Clonogenic Mesenchymal Stem Cells on Immunomodulation of Lymphocyte Subsets
title_sort differences of clonogenic mesenchymal stem cells on immunomodulation of lymphocyte subsets
url http://dx.doi.org/10.1155/2018/7232717
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