Intrathecal Autologous ADRC Treatment of Autoimmune Refractory Epilepsy (EPIMSC)
Primary Purpose
Refractory Epilepsy
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
ADRC transplantation in autoimmune refractory epilepsy
Sponsored by
About this trial
This is an interventional treatment trial for Refractory Epilepsy focused on measuring autoimmune epilepsy, refractory epilepsy, ADRC, mezenchymal stem cells, anti-neuronal antibody, Rasmussen encephality, adipose derived regenerative stem cells
Eligibility Criteria
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
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Experimental group
Arm Description
Autologous ADRC transplantation in autoimmune refractory epilepsy
Outcomes
Primary Outcome Measures
Rate of epileptic seizures
recording of epileptic seizures frequency, EEG
Secondary Outcome Measures
Intelligence test
The Leiter contains 10 subtests organized into four domains: Fluid Intelligence Visualization, Memory, Attention
School progress
teacher references
Full Information
NCT ID
NCT03676569
First Posted
September 14, 2018
Last Updated
April 14, 2020
Sponsor
Mossakowski Medical Research Centre Polish Academy of Sciences
Collaborators
Institute of Mother and Child, Warsaw, Poland
1. Study Identification
Unique Protocol Identification Number
NCT03676569
Brief Title
Intrathecal Autologous ADRC Treatment of Autoimmune Refractory Epilepsy
Acronym
EPIMSC
Official Title
Intrathecal Autologous Adipose Derived Regenerative Cells Treatment of Autoimmune Determined Refractory Epilepsy - Evaluation of Safety and Efficacy
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
November 15, 2015 (Actual)
Primary Completion Date
April 14, 2019 (Actual)
Study Completion Date
April 14, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mossakowski Medical Research Centre Polish Academy of Sciences
Collaborators
Institute of Mother and Child, Warsaw, Poland
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Epilepsy
Keywords
autoimmune epilepsy, refractory epilepsy, ADRC, mezenchymal stem cells, anti-neuronal antibody, Rasmussen encephality, adipose derived regenerative stem cells
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Model Description
Experimental clinical treatment
Masking
None (Open Label)
Allocation
N/A
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Experimental group
Arm Type
Experimental
Arm Description
Autologous ADRC transplantation in autoimmune refractory epilepsy
Intervention Type
Biological
Intervention Name(s)
ADRC transplantation in autoimmune refractory epilepsy
Primary Outcome Measure Information:
Title
Rate of epileptic seizures
Description
recording of epileptic seizures frequency, EEG
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Intelligence test
Description
The Leiter contains 10 subtests organized into four domains: Fluid Intelligence Visualization, Memory, Attention
Time Frame
3 months
Title
School progress
Description
teacher references
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Radiological assesment
Description
MRI
Time Frame
12 months
Title
The level of antineural antibodies
Description
protein 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
Time Frame
3 months
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dorota Antczak-Marach, M.D.
Organizational Affiliation
Institute of Mother and Child
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ewa Sawicka, Prof.
Organizational Affiliation
Institute of Mother and Child
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32190059
Citation
Szczepanik E, Mierzewska H, Antczak-Marach D, Figiel-Dabrowska A, Terczynska I, Tryfon J, Krzesniak N, Noszczyk BH, Sawicka E, Domanska-Janik K, Sarnowska A. Intrathecal Infusion of Autologous Adipose-Derived Regenerative Cells in Autoimmune Refractory Epilepsy: Evaluation of Safety and Efficacy. Stem Cells Int. 2020 Jan 3;2020:7104243. doi: 10.1155/2020/7104243. eCollection 2020.
Results Reference
result
Learn more about this trial
Intrathecal Autologous ADRC Treatment of Autoimmune Refractory Epilepsy
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