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...
Main Authors: | , , , , , , , , , , , , , , , , |
---|---|
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 |
id |
doaj-27065a2aef4d4369a465302c97540e44 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT sarallufriu randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT mariasepulveda randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT yolandablanco randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT pedromarin randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT beatrizmoreno randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT joanberenguer randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT inigogabilondo randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT eloymartinezheras randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT nuriasolavalls randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT joanalbertarnaiz randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT enriquejandreu randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT begonafernandez randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT santibullich randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT bernardosanchezdalmau randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT francescgraus randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT pablovilloslada randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis AT albertsaiz randomizedplacebocontrolledphaseiitrialofautologousmesenchymalstemcellsinmultiplesclerosis |
_version_ |
1725804734690885632 |