Neural stem cell transplantation in patients with progressive multiple sclerosis: an open-label, phase 1 study
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Published:2023-01
Issue:1
Volume:29
Page:75-85
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ISSN:1078-8956
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Container-title:Nature Medicine
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language:en
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Short-container-title:Nat Med
Author:
Genchi AngelaORCID, Brambilla Elena, Sangalli Francesca, Radaelli Marta, Bacigaluppi MarcoORCID, Furlan RobertoORCID, Andolfo Annapaola, Drago Denise, Magagnotti Cinzia, Scotti Giulia MariaORCID, Greco Raffaella, Vezzulli PaoloORCID, Ottoboni Linda, Bonopane Marco, Capilupo Daniela, Ruffini FrancescaORCID, Belotti Daniela, Cabiati Benedetta, Cesana Stefania, Matera Giada, Leocani Letizia, Martinelli Vittorio, Moiola Lucia, Vago LucaORCID, Panina-Bordignon Paola, Falini Andrea, Ciceri Fabio, Uglietti Anna, Sormani Maria PiaORCID, Comi Giancarlo, Battaglia Mario Alberto, Rocca Maria A.ORCID, Storelli Loredana, Pagani ElisabettaORCID, Gaipa GiuseppeORCID, Martino GianvitoORCID
Abstract
AbstractInnovative 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 tohfNPCs at 2-year follow-up, clearly demonstrating thathfNPC therapy in PMS is feasible, safe and tolerable. Exploratory secondary analyses showed a lower rate of brain atrophy in patients receiving the highest dosage ofhfNPCs 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 ofhfNPCs in a larger cohort of patients.
Funder
Fondazione Italiana Sclerosi Multipla Fondazione Cariplo Associazione Amici Centro Sclerosi Multipla (ACeSM), BMW Italia, Fondazione Tettamanti Menotti De Marchi ONLUS, Comitato Stefano Verri ONLUS, and Comitato Maria Letizia Verga ONLUS.
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
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