Phase I Trial of Intrathecal Mesenchymal Stem Cell-derived Neural Progenitors in Progressive Multiple Sclerosis

被引:118
作者
Harris, Violaine K. [1 ]
Stark, James [1 ]
Vyshkina, Tamara [1 ]
Blackshear, Leslie [1 ]
Joo, Gloria [1 ]
Stefanova, Valentina [1 ]
Sara, Gabriel [2 ]
Sadiq, Saud A. [1 ]
机构
[1] Tisch Multiple Sclerosis Res Ctr New York, 521 West 57th St,4th Floor, New York, NY 10019 USA
[2] Mt Sinai Hosp, Dept Hematol & Med Oncol, New York, NY 10029 USA
关键词
Multiple sclerosis; Mesenchymal stem cells; Intrathecal; Clinical trial; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MARROW STROMAL CELLS; AMYOTROPHIC-LATERAL-SCLEROSIS; CENTRAL-NERVOUS-SYSTEM; THERAPEUTIC PROPERTIES; OPEN-LABEL; SAFETY; MICE; TRANSPLANTATION; MECHANISMS;
D O I
10.1016/j.ebiom.2018.02.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Multiple sclerosis (MS) is an immune-mediated demyelinating disease of the central nervous systemand is one of the leading causes of disability in young adults. Cell therapy is emerging as a therapeutic strategy to promote repair and regeneration in patients with disability associated with progressive MS. Methods: We conducted a phase I open-label clinical trial investigating the safety and tolerability of autologous bone marrow mesenchymal stem cell-derived neural progenitor (MSC-NP) treatment in 20 patients with progressive MS. MSC-NPs were administered intrathecally (IT) in three separate doses of up to 1 x 10(7) cells per dose, spaced three months apart. The primary endpointwas to assess safety and tolerability of the treatment. Expanded disability status scale (EDSS), timed 25-ft walk (T25FW), muscle strength, and urodynamic testing were used to evaluate treatment response. This trial is registered with ClinicalTrials. gov, number NCT01933802. Findings: IT MSC-NP treatment was safe and well tolerated. The 20 enrolled subjects completed all 60 planned treatments without serious adverse effects. Minor adverse events included transient fever and mild headaches usually resolving in <24 h. Post-treatment disability score analysis demonstrated improved median EDSS suggesting possible efficacy. Positive trends were more frequently observed in the subset of SPMS patients and in ambulatory subjects (EDSS <= 6.5). In addition, 70% and 50% of the subjects demonstrated improved muscle strength and bladder function, respectively, following IT MSC-NP treatment. Interpretation: The possible reversal of disability thatwas observed in a subset of patientswarrants a larger phase II placebo-controlled study to establish efficacy of IT MSC-NP treatment in patients with MS. Funding source: The Damial Foundation. (C) 2018 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:23 / 30
页数:8
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