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    Por favor, use este identificador para citar o enlazar este ítem:https://uvadoc.uva.es/handle/10324/68991

    Título
    Intravitreal allogeneic mesenchymal stem cells: a non-randomized phase II clinical trial for acute non-arteritic optic neuropathy
    Autor
    Pastor Jimeno, José CarlosAutoridad UVA
    Pastor Idoate, SalvadorAutoridad UVA
    López Paniagua, MarinaAutoridad UVA Orcid
    Para Prieto, Marta
    Blázquez Araúzo, Francisco
    Murgui Tejedor, EstherAutoridad UVA
    García, Verónica
    Coco Martín, Rosa MaríaAutoridad UVA Orcid
    Año del Documento
    2023
    Editorial
    BMC Part of Springer Nature
    Descripción
    Producción Científica
    Documento Fuente
    Stem Cell Research & Therapy, September 2023, vol. 14, n. 1, 261
    Resumen
    BACKGROUND: An effective treatment for acute non-arteritic ischemic optic neuropathy (NA-AION) has not been known or proven yet. Previous studies have suggested a neuroprotective effect of allogeneic bone marrow-derived mesenchymal stem cells. This study aims to report the results of a clinical trial on patients with acute non-arteritic optic neuropathy (NA-AION) treated with an intravitreal injection of allogeneic bone marrow-derived mesenchymal stem cells (BM-MSCs) (MSV®). METHODS: We conducted a prospective, non-randomized, clinical phase-II study (Eudra CT number 2016-003029-40; ClinicalTrials.gov Registry NCT03173638) that included 5 patients with acute unilateral NA-AION diagnosed within 2 weeks after symptom onset and who received an intravitreal injection of allogeneic BM-MSCs (0.05 ml; cell concentration: 1.5 × 106cells/mL). The patients underwent regular ophthalmological examinations and were followed for one year. RESULTS: In this trial, allogeneic BM-MSCs appeared to be safe as no patients developed signs of acute nor chronic intraocular inflammation or a significant change in intraocular pressure, although an epiretinal membrane was developed in one patient. A retrolental aggregate formed shortly after the injection spontaneously disappeared within a few weeks in another phakic patient, leaving a subcapsular cataract. Visual improvement was noted in 4 patients, and amplitudes of P100 on the visually evoked potentials recordings increased in three patients. The retinal nerve fiber layer and macular ganglion cell layer thicknesses significantly decreased during the follow-up. CONCLUSIONS Besides the development of an epiretinal membrane in one patient, the intravitreal application of allogeneic BM-MSCs appeared to be intraocularly well tolerated. Consequently, not only NA-AION but also BM-MSCs deserve more clinical investigational resources and a larger randomized multicenter trial that would provide stronger evidence both about safety and the potential therapeutic efficacy of intravitreally injected allogeneic BM-MSCsin acute NA-AION. TRIAL REGISTRATION: Safety Assessment of Intravitreal Mesenchymal Stem Cells for Acute Non-Arteritic Anterior Ischemic Optic Neuropathy (NEUROSTEM). NCT03173638. Registered June 02, 2017 https:// clini caltr ials. gov/ ct2/ show/ NCT03173638.
    Materias Unesco
    3201.09 Oftalmología
    Palabras Clave
    NA-AION
    Acute anterior ischemic optic neuropathy
    MSV®
    Allogeneic bone marrow-derived mesenchymal stem cells
    BM-MSCs
    Bone marrow mesenchymal stem cells
    ISSN
    1757-6512
    Revisión por pares
    SI
    DOI
    10.1186/s13287-023-03500-7
    Patrocinador
    Strategic Action in Health of the Institute of Health Carlos III,PIC18/00018, Jose C. Pastor, Department of Regional Health of the Castilla y Léon Government, GRS 1928/A/19, Jose C. Pastor, Consejería de Educación, Junta de Castilla y León, Grant VA077P17, Jose C. Pastor
    Version del Editor
    https://stemcellres.biomedcentral.com/articles/10.1186/s13287-023-03500-7
    Propietario de los Derechos
    © The Author(s) 2023
    Idioma
    eng
    URI
    https://uvadoc.uva.es/handle/10324/68991
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    openAccess
    Aparece en las colecciones
    • Retina - Artículos de Revista [13]
    • IOBA - Artículos de revista [80]
    • DEP11 - Artículos de revista [242]
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