Autologous olfactory ensheathing cell transplantation in human paraplegia: a 3-year clinical trial

Аутологичная трансплантация обонятельных оболочечных клеток при параплегии у человека: 3-летнее клиническое исследование
Alan Mackay‐Sim, François Féron, J. Cochrane, Louise Bassingthwaighte, C E Bayliss, William E. Davies, Patricia Fronek, Colin M. Gray, Graham Kerr, P. Licina, Adrian Nowitzke, Chris Perry, Peter A. Silburn, Susan Urquhart, Timothy Geraghty
2008-08-08

Phase I/IIa clinical trialautologous cell therapyhuman paraplegiaolfactory ensheathing cell transplantationspinal cord injury
Olfactory ensheathing cells show promise in preclinical animal models as a cell transplantation therapy for repair of the injured spinal cord. This is a report of a clinical trial of autologous transplantation of olfactory ensheathing cells into the spinal cord in six patients with complete, thoracic paraplegia. We previously reported on the methods of surgery and transplantation and the safety aspects of the trial 1 year after transplantation. Here we address the overall design of the trial and the safety of the procedure, assessed during a period of 3 years following the transplantation surgery. All patients were assessed at entry into the trial and regularly during the period of the trial. Clinical assessments included medical, psychosocial, radiological and neurological, as well as specialized tests of neurological and functional deficits (standard American Spinal Injury Association and Functional Independence Measure assessments). Quantitative test included neurophysiological tests of sensory and motor function below the level of injury. The trial was a Phase I/IIa design whose main aim was to test the feasibility and safety of transplantation of autologous olfactory ensheathing cells into the injured spinal cord in human paraplegia. The design included a control group who did not receive surgery, otherwise closely matched to the transplant recipient group. This group acted as a control for the assessors, who were blind to the treatment status of the patients. The control group also provided the opportunity for preliminary assessment of the efficacy of the transplantation. There were no adverse findings 3 years after autologous transplantation of olfactory ensheathing cells into spinal cords injured at least 2 years prior to transplantation. The magnetic resonance images (MRIs) at 3 years showed no change from preoperative MRIs or intervening MRIs at 1 and 2 years, with no evidence of any tumour of introduced cells and no development of post-traumatic syringomyelia or other adverse radiological findings. There were no significant functional changes in any patients and no neuropathic pain. In one transplant recipient, there was an improvement over 3 segments in light touch and pin prick sensitivity bilaterally, anteriorly and posteriorly. We conclude that transplantation of autologous olfactory ensheathing cells into the injured spinal cord is feasible and is safe up to 3 years of post-implantation, however, this conclusion should be considered preliminary because of the small number of trial patients.
1
A Phase I/IIa trial evaluated the feasibility and safety of autologous olfactory ensheathing cell transplantation in six patients with chronic, complete thoracic paraplegia.
2
A closely matched nonsurgical control group enabled blinded assessor comparisons and preliminary evaluation of transplantation efficacy.
3
No adverse findings were detected during the three years following transplantation into spinal cords injured at least two years earlier.
4
The trial used repeated medical, psychosocial, radiological, neurological, neurophysiological, and functional assessments, including standard ASIA and Functional Independence Measure evaluations.
5
Three-year MRI scans showed no changes from preoperative or earlier follow-up images, with no tumors from introduced cells or post-traumatic syrinx development.

Autologous olfactory ensheathing cell transplantation into the injured spinal cord of humans with complete thoracic paraplegia

The 3-year feasibility and safety of the transplantation procedure, with preliminary assessment of neurological and functional efficacy

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2008-08-08
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Alan Mackay‐Sim
François Féron
J. Cochrane
Louise Bassingthwaighte
C E Bayliss
William E. Davies
Patricia Fronek
Colin M. Gray
Graham Kerr
P. Licina
Adrian Nowitzke
Chris Perry
Peter A. Silburn
Susan Urquhart
Timothy Geraghty
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