Intrathecal Infusion of Autologous Adipose-Derived Regenerative Cells in Autoimmune Refractory Epilepsy: Evaluation of Safety and Efficacy

Author:

Szczepanik Elzbieta1,Mierzewska Hanna1,Antczak-Marach Dorota1,Figiel-Dabrowska Anna2,Terczynska Iwona1,Tryfon Jolanta1,Krzesniak Natalia3,Noszczyk Bartlomiej Henryk3,Sawicka Ewa4,Domanska-Janik Krystyna2ORCID,Sarnowska Anna2ORCID

Affiliation:

1. Clinic of Child and Adolescent Neurology, Institute of Mother and Child, Poland

2. Mossakowski Medical Research Centre, Polish Academy of Sciences, Poland

3. Department of Plastic Surgery Centre of Postgraduate Medical Education, Poland

4. Clinic of Child and Adolescent Surgery, Institute of Mother and Child, Poland

Abstract

Objective/Purpose. Evaluation of efficacy and safety of autologous adipose-derived regenerative cells (ADRCs) treatment in autoimmune refractory epilepsy. Patients. Six patients with proven or probable autoimmune refractory epilepsy (2 with Rasmussen encephalitis, 2 with antineuronal autoantibodies in serum, and 2 with possible FIRES) were included in the project with approval of the Bioethics Committee. Method. Intrathecal injection of autologous ADRC acquired through liposuction followed by enzymatic isolation was performed. The procedure was repeated 3 times every 3 months with each patient. Neurological status, brain MRI, cognitive function, and antiepileptic effect were monitored during 12 months. Results. Immediately after the procedure, all patients were in good condition. In some cases, transient mildly elevated body temperature, pain in regions of liposuction, and slight increasing number of seizures during 24 hours were observed. During the next months, some improvements in school, social functioning, and manual performance were observed in all patients. One patient has been seizure free up to the end of trial. In other patients, frequency of seizures was different: from reduced number to the lack of improvement (3-year follow-up). Conclusion. Autologous ADRC therapy may emerge as a promising option for some patients with autoimmune refractory epilepsy. Based on our trial and other clinical data, the therapy appears to be safe and feasible. Antiepileptic efficacy proved to be various; however, some abilities improved in all children. No signs of psychomotor regression were observed during the first year following the treatment.

Funder

Narodowe Centrum Badań i Rozwoju

Publisher

Hindawi Limited

Subject

Cell Biology,Molecular Biology

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