Preclinical Safety Evaluation of Intranasally Delivered Human Mesenchymal Stem Cells in Juvenile Mice.
Yolanda AguileraNuria Mellado-DamasLaura Olmedo-MorenoVíctor LópezConcepción Panadero-MorónMarina BenitoHugo Guerrero-CázaresCatalina Márquez-VegaAlejandro Martín-MontalvoVivian Capilla-GonzálezPublished in: Cancers (2021)
Mesenchymal stem cell (MSC)-based therapy is a promising therapeutic approach in the management of several pathologies, including central nervous system diseases. Previously, we demonstrated the therapeutic potential of human adipose-derived MSCs for neurological sequelae of oncological radiotherapy using the intranasal route as a non-invasive delivery method. However, a comprehensive investigation of the safety of intranasal MSC treatment should be performed before clinical applications. Here, we cultured human MSCs in compliance with quality control standards and administrated repeated doses of cells into the nostrils of juvenile immunodeficient mice, mimicking the design of a subsequent clinical trial. Short- and long-term effects of cell administration were evaluated by in vivo and ex vivo studies. No serious adverse events were reported on mouse welfare, behavioral performances, and blood plasma analysis. Magnetic resonance study and histological analysis did not reveal tumor formation or other abnormalities in the examined organs of mice receiving MSCs. Biodistribution study reveals a progressive disappearance of transplanted cells that was further supported by an absent expression of human GAPDH gene in the major organs of transplanted mice. Our data indicate that the intranasal application of MSCs is a safe, simple and non-invasive strategy and encourage its use in future clinical trials.
Keyphrases
- mesenchymal stem cells
- endothelial cells
- clinical trial
- umbilical cord
- magnetic resonance
- induced apoptosis
- pluripotent stem cells
- cell therapy
- induced pluripotent stem cells
- quality control
- high fat diet induced
- bone marrow
- poor prognosis
- multiple sclerosis
- magnetic resonance imaging
- single cell
- genome wide
- computed tomography
- metabolic syndrome
- radiation therapy
- signaling pathway
- oxidative stress
- early stage
- type diabetes
- cell cycle arrest
- cell proliferation
- blood brain barrier
- current status
- locally advanced
- copy number
- data analysis
- brain injury
- binding protein
- combination therapy