New Therapy for Spinal Cord Injury: Autologous Genetically-Enriched Leucoconcentrate Integrated with Epidural Electrical Stimulation.
Rustem R IslamovFarid BashirovAndrei A IzmailovFilip FadeevVage MarkosyanMikhail SokolovMaksim ShmarovDenis LogunovBoris NaroditskyIgor A LavrovPublished in: Cells (2022)
The contemporary strategy for spinal cord injury (SCI) therapy aims to combine multiple approaches to control pathogenic mechanisms of neurodegeneration and stimulate neuroregeneration. In this study, a novel regenerative approach using an autologous leucoconcentrate enriched with transgenes encoding vascular endothelial growth factor (VEGF), glial cell line-derived neurotrophic factor (GDNF), and neural cell adhesion molecule (NCAM) combined with supra- and sub-lesional epidural electrical stimulation (EES) was tested on mini-pigs similar in morpho-physiological scale to humans. The complex analysis of the spinal cord recovery after a moderate contusion injury in treated mini-pigs compared to control animals revealed: better performance in behavioural and joint kinematics, restoration of electromyography characteristics, and improvement in selected immunohistology features related to cell survivability, synaptic protein expression, and glial reorganization above and below the injury. These results for the first time demonstrate the positive effect of intravenous infusion of autologous genetically-enriched leucoconcentrate producing recombinant molecules stimulating neuroregeneration combined with neuromodulation by translesional multisite EES on the restoration of the post-traumatic spinal cord in mini-pigs and suggest the high translational potential of this novel regenerative therapy for SCI patients.
Keyphrases
- spinal cord injury
- spinal cord
- cell therapy
- neuropathic pain
- vascular endothelial growth factor
- stem cells
- cell adhesion
- mesenchymal stem cells
- bone marrow
- end stage renal disease
- newly diagnosed
- endothelial cells
- chronic kidney disease
- single cell
- ejection fraction
- platelet rich plasma
- low dose
- high dose
- high intensity
- climate change
- replacement therapy
- cell free