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Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety
Mesenchymal stromal cells (MSCs) are used as salvage therapy to treat steroid-refractory acute graft-versus-host disease (aGvHD). We studied the immunological response to MSC treatment in 16 aGvHD patients by assessing lymphocyte profiles and three proposed aGvHD serum markers during the MSC treatme...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834657/ https://www.ncbi.nlm.nih.gov/pubmed/29516024 http://dx.doi.org/10.1016/j.omtm.2018.02.001 |
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author | Keto, Joni Kaartinen, Tanja Salmenniemi, Urpu Castrén, Johanna Partanen, Jukka Hänninen, Arno Korhonen, Matti Lähteenmäki, Kaarina Itälä-Remes, Maija Nystedt, Johanna |
author_facet | Keto, Joni Kaartinen, Tanja Salmenniemi, Urpu Castrén, Johanna Partanen, Jukka Hänninen, Arno Korhonen, Matti Lähteenmäki, Kaarina Itälä-Remes, Maija Nystedt, Johanna |
author_sort | Keto, Joni |
collection | PubMed |
description | Mesenchymal stromal cells (MSCs) are used as salvage therapy to treat steroid-refractory acute graft-versus-host disease (aGvHD). We studied the immunological response to MSC treatment in 16 aGvHD patients by assessing lymphocyte profiles and three proposed aGvHD serum markers during the MSC treatment. Surprisingly, there were no obvious differences in the lymphocyte profiles between the responders and non-responders. The numbers of T, B, and NK cells were below the normal reference interval in all patients. CD4(+) T helper (Th) cell levels remained particularly low throughout the follow-up period. The relative proportion of Th1 cells decreased, while regulatory T cells remained unaltered, and only very few Th2 and Th17 cells could be detected. Serum concentrations of regenerating islet-derived protein 3-alpha, cytokeratin-18 fragments (CK18F), and elafin were significantly elevated in patient samples compared with healthy controls, but only CK18F showed any potential in the prediction of patients’ response to MSCs. No obvious markers for MSC therapy response were revealed in this study, but the results suggest that allogeneic MSCs do not provoke overt T cell-mediated immune responses at least in immunosuppressed aGvHD patients. The results advocate for the safety of MSC therapy and bring new insights in MSC immunomodulation mechanisms. |
format | Online Article Text |
id | pubmed-5834657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-58346572018-03-07 Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety Keto, Joni Kaartinen, Tanja Salmenniemi, Urpu Castrén, Johanna Partanen, Jukka Hänninen, Arno Korhonen, Matti Lähteenmäki, Kaarina Itälä-Remes, Maija Nystedt, Johanna Mol Ther Methods Clin Dev Article Mesenchymal stromal cells (MSCs) are used as salvage therapy to treat steroid-refractory acute graft-versus-host disease (aGvHD). We studied the immunological response to MSC treatment in 16 aGvHD patients by assessing lymphocyte profiles and three proposed aGvHD serum markers during the MSC treatment. Surprisingly, there were no obvious differences in the lymphocyte profiles between the responders and non-responders. The numbers of T, B, and NK cells were below the normal reference interval in all patients. CD4(+) T helper (Th) cell levels remained particularly low throughout the follow-up period. The relative proportion of Th1 cells decreased, while regulatory T cells remained unaltered, and only very few Th2 and Th17 cells could be detected. Serum concentrations of regenerating islet-derived protein 3-alpha, cytokeratin-18 fragments (CK18F), and elafin were significantly elevated in patient samples compared with healthy controls, but only CK18F showed any potential in the prediction of patients’ response to MSCs. No obvious markers for MSC therapy response were revealed in this study, but the results suggest that allogeneic MSCs do not provoke overt T cell-mediated immune responses at least in immunosuppressed aGvHD patients. The results advocate for the safety of MSC therapy and bring new insights in MSC immunomodulation mechanisms. American Society of Gene & Cell Therapy 2018-02-08 /pmc/articles/PMC5834657/ /pubmed/29516024 http://dx.doi.org/10.1016/j.omtm.2018.02.001 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Keto, Joni Kaartinen, Tanja Salmenniemi, Urpu Castrén, Johanna Partanen, Jukka Hänninen, Arno Korhonen, Matti Lähteenmäki, Kaarina Itälä-Remes, Maija Nystedt, Johanna Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety |
title | Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety |
title_full | Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety |
title_fullStr | Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety |
title_full_unstemmed | Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety |
title_short | Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety |
title_sort | immunomonitoring of msc-treated gvhd patients reveals only moderate potential for response prediction but indicates treatment safety |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834657/ https://www.ncbi.nlm.nih.gov/pubmed/29516024 http://dx.doi.org/10.1016/j.omtm.2018.02.001 |
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