The use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: Results from compassionate use in real‐life settings

Abstract Muscular dystrophies are genetically determined progressive diseases with no cause‐related treatment and limited supportive treatment. Although stem cells cannot resolve the underlying genetic conditions, their wide‐ranging therapeutic properties may ameliorate the consequences of the invol...

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Main Authors: Beata Świątkowska‐Flis, Izabela Zdolińska‐Malinowska, Dominika Sługocka, Dariusz Boruczkowski
Format: Article
Language:English
Published: Wiley 2021-10-01
Series:Stem Cells Translational Medicine
Subjects:
Online Access:https://doi.org/10.1002/sctm.21-0027
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spelling doaj-43624a95146f4c8dae5b9d5dc0a4d5872021-09-23T13:08:08ZengWileyStem Cells Translational Medicine2157-65642157-65802021-10-0110101372138310.1002/sctm.21-0027The use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: Results from compassionate use in real‐life settingsBeata Świątkowska‐Flis0Izabela Zdolińska‐Malinowska1Dominika Sługocka2Dariusz Boruczkowski3Polish Center of Cell Therapy and Immunotherapy in Częstochowa, CM Klara Częstochowa PolandPolski Bank Komórek Macierzystych (FamiCord Group) Warsaw PolandPolish Center of Cell Therapy and Immunotherapy in Częstochowa, CM Klara Częstochowa PolandPolski Bank Komórek Macierzystych (FamiCord Group) Warsaw PolandAbstract Muscular dystrophies are genetically determined progressive diseases with no cause‐related treatment and limited supportive treatment. Although stem cells cannot resolve the underlying genetic conditions, their wide‐ranging therapeutic properties may ameliorate the consequences of the involved mutations (oxidative stress, inflammation, mitochondrial dysfunction, necrosis). In this study, we administered advanced therapy medicinal product containing umbilical cord‐derived mesenchymal stem cells (UC‐MSCs) to 22 patients with muscular dystrophies. Patients received one to five intravenous and/or intrathecal injections per treatment course in up to two courses every 2 months. Four standard doses of 10, 20, 30, or 40 × 106 UC‐MSCs per injection were used; the approximate dose per kilogram was 1 × 106 UC‐MSCs. Muscle strength was measured with a set of CQ Dynamometer computerized force meters (CQ Elektronik System, Czernica, Poland). Statistical analysis of muscle strength in the whole group showed significant improvement in the right upper limb (+4.0 N); left hip straightening (+4.5 N) and adduction (+0.5 N); right hip straightening (+1.0 N), bending (+7.5 N), and adduction (+2.5 N); right knee straightening (+8.5 N); left shoulder revocation (+13.0 N), straightening (+5.5 N), and bending (+6.5 N); right shoulder adduction (+3.0 N), revocation (+10.5 N), and bending (+5 N); and right elbow straightening (+9.5 N); all these differences were statistically significant. In six patients (27.3%) these changes led to improvement in gait analysis or movement scale result. Only one patient experienced transient headache and lower back pain after the last administration. In conclusion, UC‐MSC therapy may be considered as a therapeutic option for these patients.https://doi.org/10.1002/sctm.21-0027dystrophymuscular diseasesmusculoskeletal disordersstem cell therapyWharton's jelly
collection DOAJ
language English
format Article
sources DOAJ
author Beata Świątkowska‐Flis
Izabela Zdolińska‐Malinowska
Dominika Sługocka
Dariusz Boruczkowski
spellingShingle Beata Świątkowska‐Flis
Izabela Zdolińska‐Malinowska
Dominika Sługocka
Dariusz Boruczkowski
The use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: Results from compassionate use in real‐life settings
Stem Cells Translational Medicine
dystrophy
muscular diseases
musculoskeletal disorders
stem cell therapy
Wharton's jelly
author_facet Beata Świątkowska‐Flis
Izabela Zdolińska‐Malinowska
Dominika Sługocka
Dariusz Boruczkowski
author_sort Beata Świątkowska‐Flis
title The use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: Results from compassionate use in real‐life settings
title_short The use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: Results from compassionate use in real‐life settings
title_full The use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: Results from compassionate use in real‐life settings
title_fullStr The use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: Results from compassionate use in real‐life settings
title_full_unstemmed The use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: Results from compassionate use in real‐life settings
title_sort use of umbilical cord‐derived mesenchymal stem cells in patients with muscular dystrophies: results from compassionate use in real‐life settings
publisher Wiley
series Stem Cells Translational Medicine
issn 2157-6564
2157-6580
publishDate 2021-10-01
description Abstract Muscular dystrophies are genetically determined progressive diseases with no cause‐related treatment and limited supportive treatment. Although stem cells cannot resolve the underlying genetic conditions, their wide‐ranging therapeutic properties may ameliorate the consequences of the involved mutations (oxidative stress, inflammation, mitochondrial dysfunction, necrosis). In this study, we administered advanced therapy medicinal product containing umbilical cord‐derived mesenchymal stem cells (UC‐MSCs) to 22 patients with muscular dystrophies. Patients received one to five intravenous and/or intrathecal injections per treatment course in up to two courses every 2 months. Four standard doses of 10, 20, 30, or 40 × 106 UC‐MSCs per injection were used; the approximate dose per kilogram was 1 × 106 UC‐MSCs. Muscle strength was measured with a set of CQ Dynamometer computerized force meters (CQ Elektronik System, Czernica, Poland). Statistical analysis of muscle strength in the whole group showed significant improvement in the right upper limb (+4.0 N); left hip straightening (+4.5 N) and adduction (+0.5 N); right hip straightening (+1.0 N), bending (+7.5 N), and adduction (+2.5 N); right knee straightening (+8.5 N); left shoulder revocation (+13.0 N), straightening (+5.5 N), and bending (+6.5 N); right shoulder adduction (+3.0 N), revocation (+10.5 N), and bending (+5 N); and right elbow straightening (+9.5 N); all these differences were statistically significant. In six patients (27.3%) these changes led to improvement in gait analysis or movement scale result. Only one patient experienced transient headache and lower back pain after the last administration. In conclusion, UC‐MSC therapy may be considered as a therapeutic option for these patients.
topic dystrophy
muscular diseases
musculoskeletal disorders
stem cell therapy
Wharton's jelly
url https://doi.org/10.1002/sctm.21-0027
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