Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis.

Uncontrolled studies of mesenchymal stem cells (MSCs) in multiple sclerosis suggested some beneficial effect. In this randomized, double-blind, placebo-controlled, crossover phase II study we investigated their safety and efficacy in relapsing-remitting multiple sclerosis patients. Efficacy was eval...

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Main Authors: Sara Llufriu, María Sepúlveda, Yolanda Blanco, Pedro Marín, Beatriz Moreno, Joan Berenguer, Iñigo Gabilondo, Eloy Martínez-Heras, Nuria Sola-Valls, Joan-Albert Arnaiz, Enrique J Andreu, Begoña Fernández, Santi Bullich, Bernardo Sánchez-Dalmau, Francesc Graus, Pablo Villoslada, Albert Saiz
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4250058?pdf=render
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spelling doaj-27065a2aef4d4369a465302c97540e442020-11-24T22:11:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01912e11393610.1371/journal.pone.0113936Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis.Sara LlufriuMaría SepúlvedaYolanda BlancoPedro MarínBeatriz MorenoJoan BerenguerIñigo GabilondoEloy Martínez-HerasNuria Sola-VallsJoan-Albert ArnaizEnrique J AndreuBegoña FernándezSanti BullichBernardo Sánchez-DalmauFrancesc GrausPablo VillosladaAlbert SaizUncontrolled studies of mesenchymal stem cells (MSCs) in multiple sclerosis suggested some beneficial effect. In this randomized, double-blind, placebo-controlled, crossover phase II study we investigated their safety and efficacy in relapsing-remitting multiple sclerosis patients. Efficacy was evaluated in terms of cumulative number of gadolinium-enhancing lesions (GEL) on magnetic resonance imaging (MRI) at 6 months and at the end of the study.Patients unresponsive to conventional therapy, defined by at least 1 relapse and/or GEL on MRI scan in past 12 months, disease duration 2 to 10 years and Expanded Disability Status Scale (EDSS) 3.0-6.5 were randomized to receive IV 1-2×10(6) bone-marrow-derived-MSCs/Kg or placebo. After 6 months, the treatment was reversed and patients were followed-up for another 6 months. Secondary endpoints were clinical outcomes (relapses and disability by EDSS and MS Functional Composite), and several brain MRI and optical coherence tomography measures. Immunological tests were explored to assess the immunomodulatory effects.At baseline 9 patients were randomized to receive MSCs (n = 5) or placebo (n = 4). One patient on placebo withdrew after having 3 relapses in the first 5 months. We did not identify any serious adverse events. At 6 months, patients treated with MSCs had a trend to lower mean cumulative number of GEL (3.1, 95% CI = 1.1-8.8 vs 12.3, 95% CI = 4.4-34.5, p = 0.064), and at the end of study to reduced mean GEL (-2.8±5.9 vs 3±5.4, p = 0.075). No significant treatment differences were detected in the secondary endpoints. We observed a non-significant decrease of the frequency of Th1 (CD4+ IFN-γ+) cells in blood of MSCs treated patients.Bone-marrow-MSCs are safe and may reduce inflammatory MRI parameters supporting their immunomodulatory properties. ClinicalTrials.gov NCT01228266.http://europepmc.org/articles/PMC4250058?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sara Llufriu
María Sepúlveda
Yolanda Blanco
Pedro Marín
Beatriz Moreno
Joan Berenguer
Iñigo Gabilondo
Eloy Martínez-Heras
Nuria Sola-Valls
Joan-Albert Arnaiz
Enrique J Andreu
Begoña Fernández
Santi Bullich
Bernardo Sánchez-Dalmau
Francesc Graus
Pablo Villoslada
Albert Saiz
spellingShingle Sara Llufriu
María Sepúlveda
Yolanda Blanco
Pedro Marín
Beatriz Moreno
Joan Berenguer
Iñigo Gabilondo
Eloy Martínez-Heras
Nuria Sola-Valls
Joan-Albert Arnaiz
Enrique J Andreu
Begoña Fernández
Santi Bullich
Bernardo Sánchez-Dalmau
Francesc Graus
Pablo Villoslada
Albert Saiz
Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis.
PLoS ONE
author_facet Sara Llufriu
María Sepúlveda
Yolanda Blanco
Pedro Marín
Beatriz Moreno
Joan Berenguer
Iñigo Gabilondo
Eloy Martínez-Heras
Nuria Sola-Valls
Joan-Albert Arnaiz
Enrique J Andreu
Begoña Fernández
Santi Bullich
Bernardo Sánchez-Dalmau
Francesc Graus
Pablo Villoslada
Albert Saiz
author_sort Sara Llufriu
title Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis.
title_short Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis.
title_full Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis.
title_fullStr Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis.
title_full_unstemmed Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis.
title_sort randomized placebo-controlled phase ii trial of autologous mesenchymal stem cells in multiple sclerosis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Uncontrolled studies of mesenchymal stem cells (MSCs) in multiple sclerosis suggested some beneficial effect. In this randomized, double-blind, placebo-controlled, crossover phase II study we investigated their safety and efficacy in relapsing-remitting multiple sclerosis patients. Efficacy was evaluated in terms of cumulative number of gadolinium-enhancing lesions (GEL) on magnetic resonance imaging (MRI) at 6 months and at the end of the study.Patients unresponsive to conventional therapy, defined by at least 1 relapse and/or GEL on MRI scan in past 12 months, disease duration 2 to 10 years and Expanded Disability Status Scale (EDSS) 3.0-6.5 were randomized to receive IV 1-2×10(6) bone-marrow-derived-MSCs/Kg or placebo. After 6 months, the treatment was reversed and patients were followed-up for another 6 months. Secondary endpoints were clinical outcomes (relapses and disability by EDSS and MS Functional Composite), and several brain MRI and optical coherence tomography measures. Immunological tests were explored to assess the immunomodulatory effects.At baseline 9 patients were randomized to receive MSCs (n = 5) or placebo (n = 4). One patient on placebo withdrew after having 3 relapses in the first 5 months. We did not identify any serious adverse events. At 6 months, patients treated with MSCs had a trend to lower mean cumulative number of GEL (3.1, 95% CI = 1.1-8.8 vs 12.3, 95% CI = 4.4-34.5, p = 0.064), and at the end of study to reduced mean GEL (-2.8±5.9 vs 3±5.4, p = 0.075). No significant treatment differences were detected in the secondary endpoints. We observed a non-significant decrease of the frequency of Th1 (CD4+ IFN-γ+) cells in blood of MSCs treated patients.Bone-marrow-MSCs are safe and may reduce inflammatory MRI parameters supporting their immunomodulatory properties. ClinicalTrials.gov NCT01228266.
url http://europepmc.org/articles/PMC4250058?pdf=render
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