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Neural stem cell transplantation in patients with progressive multiple sclerosis: an open-label, phase 1 study.

Angela GenchiElena BrambillaFrancesca SangalliMarta RadaelliMarco BacigaluppiRoberto FurlanAnnapaola AndolfoDenise DragoCinzia MagagnottiGiulia Maria ScottiRaffaella GrecoPaolo VezzulliLinda OttoboniMarco BonopaneDaniela CapilupoFrancesca RuffiniDaniela BelottiBenedetta CabiatiStefania CesanaGiada MateraLetizia LeocaniVittorio MartinelliLucia MoiolaLuca VagoPaola Panina-BordignonAndrea FaliniFabio CiceriAnna UgliettiMaria Pia SormaniGiancarlo ComiMario Alberto BattagliaMaria Assunta RoccaLoredana StorelliElisabetta PaganiGiuseppe GaipaGianvito Martino
Published in: Nature medicine (2023)
Innovative pro-regenerative treatment strategies for progressive multiple sclerosis (PMS), combining neuroprotection and immunomodulation, represent an unmet need. Neural precursor cells (NPCs) transplanted in animal models of multiple sclerosis have shown preclinical efficacy by promoting neuroprotection and remyelination by releasing molecules sustaining trophic support and neural plasticity. Here we present the results of STEMS, a prospective, therapeutic exploratory, non-randomized, open-label, single-dose-finding phase 1 clinical trial ( NCT03269071 , EudraCT 2016-002020-86), performed at San Raffaele Hospital in Milan, Italy, evaluating the feasibility, safety and tolerability of intrathecally transplanted human fetal NPCs (hfNPCs) in 12 patients with PMS (with evidence of disease progression, Expanded Disability Status Scale ≥6.5, age 18-55 years, disease duration 2-20 years, without any alternative approved therapy). The safety primary outcome was reached, with no severe adverse reactions related to hfNPCs at 2-year follow-up, clearly demonstrating that hfNPC therapy in PMS is feasible, safe and tolerable. Exploratory secondary analyses showed a lower rate of brain atrophy in patients receiving the highest dosage of hfNPCs and increased cerebrospinal fluid levels of anti-inflammatory and neuroprotective molecules. Although preliminary, these results support the rationale and value of future clinical studies with the highest dose of hfNPCs in a larger cohort of patients.
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