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Intrathecal Autologous ADRC Treatment of Autoimmune Refractory Epilepsy

Intrathecal Autologous Adipose Derived Regenerative Cells Treatment of Autoimmune Determined Refractory Epilepsy - Evaluation of Safety and Efficacy

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03676569
Acronym
EPIMSC
Enrollment
6
Registered
2018-09-18
Start date
2015-11-15
Completion date
2019-04-14
Last updated
2020-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Refractory Epilepsy

Keywords

autoimmune epilepsy, refractory epilepsy, ADRC, mezenchymal stem cells, anti-neuronal antibody, Rasmussen encephality, adipose derived regenerative stem cells

Brief summary

Refractory epilepsies caused by an autoimmune mechanisms lead in children to progressive neurodegeneration. Immunomodulation therapy is effective only in a half of such cases. New approaches are undertaken. It was found that ADRC (adipose derived regenerative cells) isolated from adipose tissue consist mesenchymal stem cells that act as tissue repair cells. The purpose of this experimental study is to evaluate the possibility and safety of the use of multipotent mesenchymal adipose derived regenerative cells (ADRC) in patients diagnosed with an autoimmune determined refractory epilepsy. Study protocol: Intrathecal infusions of autologous ADRC obtained after liposuction followed by isolation by Cytori system will be performed. Procedure will be repeated 3 times every 3 months in each patient. Neurological status, brain MRI, cognitive function and antiepileptic effect will be supervised during 24 months.

Detailed description

Epilepsy is a chronic neurological disorder diagnosed in about 1% of the population, or c. 400,000 patients in Poland. Autoimmune refractory epilepsy is rare but most disabled epilepsy leading to developmental regression. The belief in a positive effect of ADRCs in drug-resistant epilepsy comes from test results showing the ability of mesenchymal cells to concentrate in damaged tissues, as well as their strong immunomodulating, especially anti-inflammatory, properties. Patients with drug resistant epilepsy show decreased numbers of neurons within the epilepsy zone, with most of these being hyperactive and malfunctioning. Additionally, an inflammatory active reaction in affected brain tissue is visible. ADRC-induced activation of endogenous neurogenesis may increase chances that the epilepsy zone will be reduced, and give a positive impact as regards the neuropsychiatric disorders commonly present in patients with epilepsy. Another common process accompanying recurring epilepsy attacks is active inflammation. Per the literature, ADRCs show strong neuroprotective, immunomodulating and antiapoptotic qualities and they may potentially reduce the frequency of epilepsy attacks. Thus, a clinical trial with ADRCs, addressed to drug-resistant epilepsy sufferers would be promising in controlling the epileptic seizures and coexisting behavioral / psychiatric symptoms. The goal is to improve the quality of life of the patients and their caregivers. In patients who were diagnosed with autoimmune drug-resistant epilepsy and have met the set criteria and qualified to take part in the examination, after a formal written consent of their parents at the Clinic of Child Neurology IMC neurological examination, routine laboratory tests, EEG and neuropsychological assessment will be performed. ADRC will be obtained after liposuction and isolation with Cytori system. Before intrathecal transplantation of ADRC suspension ( 5 ml), cerebrospinal fluid will be collected for evaluation of origin protein level, oligoclonal bands, the IgG index as well as GluR3, VGKC complex/LGI1, GM1, NT-3, GAD, and NMDAR antibodies. At the same time there will be an intake of 5ml of serum to evaluate levels of immunoglobulins IgA, IgM and IgG. Procedure will be repeated 3 times every 3 months in each patient. Neurological status, brain MRI, cognitive function and antiepileptic effect will be supervised during 24 months.

Interventions

BIOLOGICALADRC transplantation in autoimmune refractory epilepsy

Sponsors

Institute of Mother and Child, Warsaw, Poland
CollaboratorOTHER
Mossakowski Medical Research Centre Polish Academy of Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Experimental clinical treatment

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Drug-resistant epilepsy confirmed in anamnesis and diagnostic tests (EEG, MR) * Children between 3 and 18 years old * Presence of antineuronal antibody in serum or CSF * Rasmussen encephalitis (proven cellular immunity pathogenesis) * Probable autoimmune pathogenesis (autoimmune diseases in family, febrile infection associated refractory epilepsy) * Willing and able to provide written informed consent (patient or legal guardian)

Exclusion criteria

* Refractory epilepsy with proven genetic or metabolic ethiology * Neoplastic disease * Active inflammatory process at the time of recruitment * Coagulation disorder * Status epilepticus * Participation in another clinical trial * Lack of willingness and ability to provide written informed consent

Design outcomes

Primary

MeasureTime frameDescription
Rate of epileptic seizures3 monthsrecording of epileptic seizures frequency, EEG

Secondary

MeasureTime frameDescription
Intelligence test3 monthsThe Leiter contains 10 subtests organized into four domains: Fluid Intelligence Visualization, Memory, Attention
School progress3 monthsteacher references

Other

MeasureTime frameDescription
Radiological assesment12 monthsMRI
The level of antineural antibodies3 monthsprotein level, oligoclonal bands, IgG index as well as GluR3, VGKC complex/LGI1, GM1, NT-3, GAD, NMDAR antibodies from cerebrospinal fluid for evaluation the origin

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026