Transplantation of Mesenchymal Stromal Cells in Patients with Amyotrophic Lateral Sclerosis: Results of Phase I/IIa Clinical Trial

Amyotrophic lateral sclerosis (ALS) is a progressive untreatable neurodegenerative disorder, leading to the death of the cortical and spinal motoneurons (MNs). Bone marrow-derived mesenchymal stem/stromal cells (BM-MSCs) may represent a new approach to slowing down the progression of ALS by providin...

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Main Authors: Eva Syková M.D., Ph.D., Dr.Sc., Petr Rychmach, Ivana Drahorádová, ŠImona Konrádová, Kateřina Růžičková, Ivan Voříšek, Serhiy Forostyak, Aleš Homola, Martin Bojar
Format: Article
Language:English
Published: SAGE Publishing 2017-04-01
Series:Cell Transplantation
Online Access:https://doi.org/10.3727/096368916X693716
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spelling doaj-7cbcaa11ce034fb7a0f42b5ff4c675902020-11-25T03:32:43ZengSAGE PublishingCell Transplantation0963-68971555-38922017-04-012610.3727/096368916X693716Transplantation of Mesenchymal Stromal Cells in Patients with Amyotrophic Lateral Sclerosis: Results of Phase I/IIa Clinical TrialEva Syková M.D., Ph.D., Dr.Sc.0Petr Rychmach1Ivana Drahorádová2ŠImona Konrádová3Kateřina Růžičková4Ivan Voříšek5Serhiy Forostyak6Aleš Homola7Martin Bojar8 Department of Neuroscience, Charles University, 2nd Medical School, Prague, Czech Republic Bioinova Ltd., Prague, Czech Republic Bioinova Ltd., Prague, Czech Republic Bioinova Ltd., Prague, Czech Republic Bioinova Ltd., Prague, Czech Republic Department of Neuroscience, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Czech Republic Department of Neuroscience, Charles University, 2nd Medical School, Prague, Czech Republic Department of Neurology, Charles University, 2nd Medical School, University Hospital at Motol, Prague, Czech Republic Department of Neurology, Charles University, 2nd Medical School, University Hospital at Motol, Prague, Czech RepublicAmyotrophic lateral sclerosis (ALS) is a progressive untreatable neurodegenerative disorder, leading to the death of the cortical and spinal motoneurons (MNs). Bone marrow-derived mesenchymal stem/stromal cells (BM-MSCs) may represent a new approach to slowing down the progression of ALS by providing neurotrophic support to host MNs and by having an anti-inflammatory effect. We have designed a prospective, nonrandomized, open-label clinical trial (phase I/IIa, EudraCT No. 2011-000362-35) to assess the safety and efficacy of autologous multipotent BM-MSCs in ALS treatment. Autologous BM-MSCs were isolated and expanded under GMP conditions. Patients received 15 ± 4.5 × 10 6 of BM-MSCs via lumbar puncture into the cerebrospinal fluid. Patients were monitored for 6 months before treatment and then for an 18-month follow-up period. Potential adverse reactions were assessed, and the clinical outcome was evaluated by the ALS functional rating scale (ALSFRS), forced vital capacity (FVC), and weakness scales (WSs) to assess muscle strength on the lower and upper extremities. In total, 26 patients were enrolled in the study and were assessed for safety; 23 patients were suitable for efficacy evaluation. After intrathecal BM-MSC application, about 30% of the patients experienced a mild to moderate headache, resembling the headaches after a standard lumbar puncture. No suspected serious adverse reactions (SUSAR) were observed. We found a reduction in ALSFRS decline at 3 months after application ( p < 0.02) that, in some cases, persisted for 6 months ( p < 0.05). In about 80% of the patients, FVC values remained stable or above 70% for a time period of 9 months. Values of WS were stable in 75% of patients at 3 months after application. Our results demonstrate that the intrathecal application of BM-MSCs in ALS patients is a safe procedure and that it can slow down progression of the disease.https://doi.org/10.3727/096368916X693716
collection DOAJ
language English
format Article
sources DOAJ
author Eva Syková M.D., Ph.D., Dr.Sc.
Petr Rychmach
Ivana Drahorádová
ŠImona Konrádová
Kateřina Růžičková
Ivan Voříšek
Serhiy Forostyak
Aleš Homola
Martin Bojar
spellingShingle Eva Syková M.D., Ph.D., Dr.Sc.
Petr Rychmach
Ivana Drahorádová
ŠImona Konrádová
Kateřina Růžičková
Ivan Voříšek
Serhiy Forostyak
Aleš Homola
Martin Bojar
Transplantation of Mesenchymal Stromal Cells in Patients with Amyotrophic Lateral Sclerosis: Results of Phase I/IIa Clinical Trial
Cell Transplantation
author_facet Eva Syková M.D., Ph.D., Dr.Sc.
Petr Rychmach
Ivana Drahorádová
ŠImona Konrádová
Kateřina Růžičková
Ivan Voříšek
Serhiy Forostyak
Aleš Homola
Martin Bojar
author_sort Eva Syková M.D., Ph.D., Dr.Sc.
title Transplantation of Mesenchymal Stromal Cells in Patients with Amyotrophic Lateral Sclerosis: Results of Phase I/IIa Clinical Trial
title_short Transplantation of Mesenchymal Stromal Cells in Patients with Amyotrophic Lateral Sclerosis: Results of Phase I/IIa Clinical Trial
title_full Transplantation of Mesenchymal Stromal Cells in Patients with Amyotrophic Lateral Sclerosis: Results of Phase I/IIa Clinical Trial
title_fullStr Transplantation of Mesenchymal Stromal Cells in Patients with Amyotrophic Lateral Sclerosis: Results of Phase I/IIa Clinical Trial
title_full_unstemmed Transplantation of Mesenchymal Stromal Cells in Patients with Amyotrophic Lateral Sclerosis: Results of Phase I/IIa Clinical Trial
title_sort transplantation of mesenchymal stromal cells in patients with amyotrophic lateral sclerosis: results of phase i/iia clinical trial
publisher SAGE Publishing
series Cell Transplantation
issn 0963-6897
1555-3892
publishDate 2017-04-01
description Amyotrophic lateral sclerosis (ALS) is a progressive untreatable neurodegenerative disorder, leading to the death of the cortical and spinal motoneurons (MNs). Bone marrow-derived mesenchymal stem/stromal cells (BM-MSCs) may represent a new approach to slowing down the progression of ALS by providing neurotrophic support to host MNs and by having an anti-inflammatory effect. We have designed a prospective, nonrandomized, open-label clinical trial (phase I/IIa, EudraCT No. 2011-000362-35) to assess the safety and efficacy of autologous multipotent BM-MSCs in ALS treatment. Autologous BM-MSCs were isolated and expanded under GMP conditions. Patients received 15 ± 4.5 × 10 6 of BM-MSCs via lumbar puncture into the cerebrospinal fluid. Patients were monitored for 6 months before treatment and then for an 18-month follow-up period. Potential adverse reactions were assessed, and the clinical outcome was evaluated by the ALS functional rating scale (ALSFRS), forced vital capacity (FVC), and weakness scales (WSs) to assess muscle strength on the lower and upper extremities. In total, 26 patients were enrolled in the study and were assessed for safety; 23 patients were suitable for efficacy evaluation. After intrathecal BM-MSC application, about 30% of the patients experienced a mild to moderate headache, resembling the headaches after a standard lumbar puncture. No suspected serious adverse reactions (SUSAR) were observed. We found a reduction in ALSFRS decline at 3 months after application ( p < 0.02) that, in some cases, persisted for 6 months ( p < 0.05). In about 80% of the patients, FVC values remained stable or above 70% for a time period of 9 months. Values of WS were stable in 75% of patients at 3 months after application. Our results demonstrate that the intrathecal application of BM-MSCs in ALS patients is a safe procedure and that it can slow down progression of the disease.
url https://doi.org/10.3727/096368916X693716
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