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临床试验/NCT03676569
NCT03676569已完成1 期

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

Mossakowski Medical Research Centre Polish Academy of Sciences0 个研究点目标入组 6 人开始时间: 2015年11月15日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
6
主要终点
Rate of epileptic seizures

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • 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)

排除标准

  • 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

结局指标

主要结局

Rate of epileptic seizures

时间窗: 3 months

recording of epileptic seizures frequency, EEG

次要结局

  • School progress(3 months)
  • Intelligence test(3 months)

研究者

发起方
Mossakowski Medical Research Centre Polish Academy of Sciences
申办方类型
Other
责任方
Principal Investigator
主要研究者

Anna Sarnowska

M.D., Ph.D.; Head of Translative Platform for Regenerative Medicine MRC Mossakowski PAS

Mossakowski Medical Research Centre Polish Academy of Sciences

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