Mesenchymal stem cells and conditioned media in the treatment of multiple sclerosis patients: Clinical, ophthalmological and radiological assessments of safety and efficacy

Summary Aims This open‐label prospective phase I/IIa clinical study used autologous bone marrow‐derived mesenchymal stromal cells (BM‐MSCs) followed by mesenchymal stromal cells conditioned media (MSC‐CM) for the first time to treat multiple sclerosis (MS) patients. The primary goal was to assess th...

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Published inCNS neuroscience & therapeutics Vol. 23; no. 11; pp. 866 - 874
Main Authors Dahbour, Said, Jamali, Fatima, Alhattab, Dana, Al‐Radaideh, Ali, Ababneh, Osama, Al‐Ryalat, Nosaiba, Al‐Bdour, Muawyeh, Hourani, Bayan, Msallam, Mohammed, Rasheed, Murad, Huneiti, Ammar, Bahou, Yacoub, Tarawneh, Emad, Awidi, Abdalla
Format Journal Article
LanguageEnglish
Published England John Wiley & Sons, Inc 01.11.2017
John Wiley and Sons Inc
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Summary:Summary Aims This open‐label prospective phase I/IIa clinical study used autologous bone marrow‐derived mesenchymal stromal cells (BM‐MSCs) followed by mesenchymal stromal cells conditioned media (MSC‐CM) for the first time to treat multiple sclerosis (MS) patients. The primary goal was to assess the safety and feasibility and the secondary was efficacy. The correlation between the MSC‐CM content and treatment outcome was investigated. Methods Ten MS patients who failed conventional therapy were enrolled. Adverse events were recorded to assess safety. The Expanded Disability Status Scale (EDSS) was the primary efficacy measurement, the secondary included clinical (25WFT, 9‐PHT), cognitive (MMS), ophthalmology (OCT, VEP), and radiological (MRI lesion and volume) tests. The MSCs‐CM concentration of 27 inflammatory biomarkers was investigated. Results The treatment protocol was well tolerated by patients. There was an overall trend of improvement in all the tests, except the lesion volume which increased significantly. A decrease of 4 and 3.5 points on the EDSS was achieved in two patients. We report a correlation between a decreased lesion number at baseline and higher IL‐6, IL‐8, and VEGF MSC‐CM content. Conclusion The used protocol was safe and feasible with possible efficacy. The addition of MSC‐CM could be related to the magnitude of EDSS improvement observed.
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NIH clinical trials registry identifier: NCT01895439.
ISSN:1755-5930
1755-5949
DOI:10.1111/cns.12759