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Systemic Infusion of Autologous Adipose Tissue-Derived Mesenchymal Stem Cells in Peritoneal Dialysis Patients: Feasibility and Safety
OBJECTIVE: Using mesenchymal stem cells (MSCs) is regarded as a new therapeutic approach for improving fibrotic diseases. the aim of this study to evaluate the feasibility and safety of systemic infusion of autologous adipose tissue-derived MSCs (AD-MSCs) in peritoneal dialysis (PD) patients with ex...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099152/ https://www.ncbi.nlm.nih.gov/pubmed/30123994 http://dx.doi.org/10.22074/cellj.2019.5591 |
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author | Alatab, Sudabeh Shekarchian, Soroosh Najafi, Iraj Moghadasali, Reza Ahmadbeigi, Naser Pourmand, Mohammad Reza Bolurieh, Tina Jaroughi, Neda Pourmand, Gholamreza Aghdami, Nasser |
author_facet | Alatab, Sudabeh Shekarchian, Soroosh Najafi, Iraj Moghadasali, Reza Ahmadbeigi, Naser Pourmand, Mohammad Reza Bolurieh, Tina Jaroughi, Neda Pourmand, Gholamreza Aghdami, Nasser |
author_sort | Alatab, Sudabeh |
collection | PubMed |
description | OBJECTIVE: Using mesenchymal stem cells (MSCs) is regarded as a new therapeutic approach for improving fibrotic diseases. the aim of this study to evaluate the feasibility and safety of systemic infusion of autologous adipose tissue-derived MSCs (AD-MSCs) in peritoneal dialysis (PD) patients with expected peritoneal fibrosis. MATERIALS AND METHODS: This study was a prospective, open-label, non-randomized, placebo-free, phase I clinical trial. Case group consisted of nine eligible renal failure patients with more than two years of history of being on PD. Autologous AD-MSCs were obtained through lipoaspiration and expanded under good manufacturing practice conditions. Patients received 1.2 ± 0.1×10(6) cell/kg of AD-MSCs via cubital vein and then were followed for six months at time points of baseline, and then 3 weeks, 6 weeks, 12 weeks, 16 weeks and 24 weeks after infusion. Clinical, biochemical and peritoneal equilibration test (PET) were performed to assess the safety and probable change in peritoneal solute transport parameters. RESULTS: No serious adverse events and no catheter-related complications were found in the participants. 14 minor reported adverse events were self-limited or subsided after supportive treatment. One patient developed an episode of peritonitis and another patient experienced exit site infection, which did not appear to be related to the procedure. A significant decrease in the rate of solute transport across peritoneal membrane was detected by PET (D/P cr=0.77 vs. 0.73, P=0.02). CONCLUSION: This study, for the first time, showed the feasibility and safety of AD-MSCs in PD patients and the potentials for positive changes in solute transport. Further studies with larger samples, longer follow-up, and randomized blind control groups to elucidate the most effective route, frequency and dose of MSCs administration, are necessary (Registration Number: IRCT2015052415841N2). |
format | Online Article Text |
id | pubmed-6099152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-60991522019-01-01 Systemic Infusion of Autologous Adipose Tissue-Derived Mesenchymal Stem Cells in Peritoneal Dialysis Patients: Feasibility and Safety Alatab, Sudabeh Shekarchian, Soroosh Najafi, Iraj Moghadasali, Reza Ahmadbeigi, Naser Pourmand, Mohammad Reza Bolurieh, Tina Jaroughi, Neda Pourmand, Gholamreza Aghdami, Nasser Cell J Original Article OBJECTIVE: Using mesenchymal stem cells (MSCs) is regarded as a new therapeutic approach for improving fibrotic diseases. the aim of this study to evaluate the feasibility and safety of systemic infusion of autologous adipose tissue-derived MSCs (AD-MSCs) in peritoneal dialysis (PD) patients with expected peritoneal fibrosis. MATERIALS AND METHODS: This study was a prospective, open-label, non-randomized, placebo-free, phase I clinical trial. Case group consisted of nine eligible renal failure patients with more than two years of history of being on PD. Autologous AD-MSCs were obtained through lipoaspiration and expanded under good manufacturing practice conditions. Patients received 1.2 ± 0.1×10(6) cell/kg of AD-MSCs via cubital vein and then were followed for six months at time points of baseline, and then 3 weeks, 6 weeks, 12 weeks, 16 weeks and 24 weeks after infusion. Clinical, biochemical and peritoneal equilibration test (PET) were performed to assess the safety and probable change in peritoneal solute transport parameters. RESULTS: No serious adverse events and no catheter-related complications were found in the participants. 14 minor reported adverse events were self-limited or subsided after supportive treatment. One patient developed an episode of peritonitis and another patient experienced exit site infection, which did not appear to be related to the procedure. A significant decrease in the rate of solute transport across peritoneal membrane was detected by PET (D/P cr=0.77 vs. 0.73, P=0.02). CONCLUSION: This study, for the first time, showed the feasibility and safety of AD-MSCs in PD patients and the potentials for positive changes in solute transport. Further studies with larger samples, longer follow-up, and randomized blind control groups to elucidate the most effective route, frequency and dose of MSCs administration, are necessary (Registration Number: IRCT2015052415841N2). Royan Institute 2019 2018-08-07 /pmc/articles/PMC6099152/ /pubmed/30123994 http://dx.doi.org/10.22074/cellj.2019.5591 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Alatab, Sudabeh Shekarchian, Soroosh Najafi, Iraj Moghadasali, Reza Ahmadbeigi, Naser Pourmand, Mohammad Reza Bolurieh, Tina Jaroughi, Neda Pourmand, Gholamreza Aghdami, Nasser Systemic Infusion of Autologous Adipose Tissue-Derived Mesenchymal Stem Cells in Peritoneal Dialysis Patients: Feasibility and Safety |
title | Systemic Infusion of Autologous Adipose Tissue-Derived
Mesenchymal Stem Cells in Peritoneal Dialysis
Patients: Feasibility and Safety |
title_full | Systemic Infusion of Autologous Adipose Tissue-Derived
Mesenchymal Stem Cells in Peritoneal Dialysis
Patients: Feasibility and Safety |
title_fullStr | Systemic Infusion of Autologous Adipose Tissue-Derived
Mesenchymal Stem Cells in Peritoneal Dialysis
Patients: Feasibility and Safety |
title_full_unstemmed | Systemic Infusion of Autologous Adipose Tissue-Derived
Mesenchymal Stem Cells in Peritoneal Dialysis
Patients: Feasibility and Safety |
title_short | Systemic Infusion of Autologous Adipose Tissue-Derived
Mesenchymal Stem Cells in Peritoneal Dialysis
Patients: Feasibility and Safety |
title_sort | systemic infusion of autologous adipose tissue-derived
mesenchymal stem cells in peritoneal dialysis
patients: feasibility and safety |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099152/ https://www.ncbi.nlm.nih.gov/pubmed/30123994 http://dx.doi.org/10.22074/cellj.2019.5591 |
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