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Sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis

BACKGROUND: Systemic sclerosis (SSc) is an autoimmune disease involving the skin and several internal organs. Most therapies available for this disease are symptomatic. Given the difficulty in treating SSc, we conducted this study to investigate the effect of combined plasmapheresis (PE) and allogen...

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Autores principales: Zhang, Huayong, Liang, Jun, Tang, Xiaojun, Wang, Dandan, Feng, Xuebing, Wang, Fan, Hua, Bingzhu, Wang, Hong, Sun, Lingyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518166/
https://www.ncbi.nlm.nih.gov/pubmed/28724445
http://dx.doi.org/10.1186/s13075-017-1373-2
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author Zhang, Huayong
Liang, Jun
Tang, Xiaojun
Wang, Dandan
Feng, Xuebing
Wang, Fan
Hua, Bingzhu
Wang, Hong
Sun, Lingyun
author_facet Zhang, Huayong
Liang, Jun
Tang, Xiaojun
Wang, Dandan
Feng, Xuebing
Wang, Fan
Hua, Bingzhu
Wang, Hong
Sun, Lingyun
author_sort Zhang, Huayong
collection PubMed
description BACKGROUND: Systemic sclerosis (SSc) is an autoimmune disease involving the skin and several internal organs. Most therapies available for this disease are symptomatic. Given the difficulty in treating SSc, we conducted this study to investigate the effect of combined plasmapheresis (PE) and allogeneic mesenchymal stem cells transplantation (MSCT) therapy on SSc. METHODS: Fourteen patients underwent three repeated PE treatments with subsequent pulse cyclophosphamide on days 1, 3 and 5. Patients received a single MSCT (1 × 10(6) cells/kg of body weight) on day 8. During follow up, evaluations performed included complete physical examination, serologic testing, and organ function. RESULTS: The mean modified Rodnan skin score (MRSS) improved from 20.1 ± 3.1 to 13.8 ± 10.2 (P < 0.001) at 12 months of follow up. Three patients had interstitial lung disease, all had improvement of lung function and improved computed tomography (CT) images after 12 months of combined therapy. This combined treatment also significantly decreased the anti-Scl70 autoantibody titer and serum transforming growth factor-β and vascular endothelial growth factor levels during follow up. CONCLUSION: The results indicate that PE combined with MSCT is a feasible treatment associated with possible clinical benefit for SSc patients. TRIAL REGISTRATION: ClinicalTrials.gov, NCT00962923. Registered on 19 August 2009.
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spelling pubmed-55181662017-08-16 Sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis Zhang, Huayong Liang, Jun Tang, Xiaojun Wang, Dandan Feng, Xuebing Wang, Fan Hua, Bingzhu Wang, Hong Sun, Lingyun Arthritis Res Ther Research Article BACKGROUND: Systemic sclerosis (SSc) is an autoimmune disease involving the skin and several internal organs. Most therapies available for this disease are symptomatic. Given the difficulty in treating SSc, we conducted this study to investigate the effect of combined plasmapheresis (PE) and allogeneic mesenchymal stem cells transplantation (MSCT) therapy on SSc. METHODS: Fourteen patients underwent three repeated PE treatments with subsequent pulse cyclophosphamide on days 1, 3 and 5. Patients received a single MSCT (1 × 10(6) cells/kg of body weight) on day 8. During follow up, evaluations performed included complete physical examination, serologic testing, and organ function. RESULTS: The mean modified Rodnan skin score (MRSS) improved from 20.1 ± 3.1 to 13.8 ± 10.2 (P < 0.001) at 12 months of follow up. Three patients had interstitial lung disease, all had improvement of lung function and improved computed tomography (CT) images after 12 months of combined therapy. This combined treatment also significantly decreased the anti-Scl70 autoantibody titer and serum transforming growth factor-β and vascular endothelial growth factor levels during follow up. CONCLUSION: The results indicate that PE combined with MSCT is a feasible treatment associated with possible clinical benefit for SSc patients. TRIAL REGISTRATION: ClinicalTrials.gov, NCT00962923. Registered on 19 August 2009. BioMed Central 2017-07-19 2017 /pmc/articles/PMC5518166/ /pubmed/28724445 http://dx.doi.org/10.1186/s13075-017-1373-2 Text en © The Author(s). 2017 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
Zhang, Huayong
Liang, Jun
Tang, Xiaojun
Wang, Dandan
Feng, Xuebing
Wang, Fan
Hua, Bingzhu
Wang, Hong
Sun, Lingyun
Sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis
title Sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis
title_full Sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis
title_fullStr Sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis
title_full_unstemmed Sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis
title_short Sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis
title_sort sustained benefit from combined plasmapheresis and allogeneic mesenchymal stem cells transplantation therapy in systemic sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518166/
https://www.ncbi.nlm.nih.gov/pubmed/28724445
http://dx.doi.org/10.1186/s13075-017-1373-2
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