First Clinical Report on the Treatment of Parkinson's Disease with Fetal Midbrain Precursor Cells

Author:

Kim Joopyoung1,Inbo Han1,Kim Hyun Sook2,Kim WonChan2,Jang Su Jin3,Min Kyunghoon4,Kim Sang Heum5,Bae Sang‐Hun6,Jeong Yun‐Hwa6,Kim Borah7,Kim Chul6,Schwarz Sigrid C.89,Schwarz Johannes810,Cho Kyung Gi1,Chung Sang‐Sup1,Moon Jisook6ORCID

Affiliation:

1. Department of Neurosurgery, CHA Bundang Medical Center CHA University Seongnam Republic of Korea

2. Department of Neurology, CHA Bundang Medical Center CHA University Seongnam Republic of Korea

3. Department of Nuclear Medicine, CHA Bundang Medical Center CHA University Seongnam Republic of Korea

4. Department of Rehabilitation Medicine, CHA Bundang Medical Center CHA University Seongnam Republic of Korea

5. Department of Neuroradiology, CHA Bundang Medical Center CHA University Seongnam Republic of Korea

6. Department of Biotechnology CHA University Seongnam Republic of Korea

7. Department of Psychiatry, CHA Bundang Medical Center CHA University Seongnam Republic of Korea

8. Department of Neurology, Technical University of Munich Klinikum rechts der Isar Munich Germany

9. German Center for Neurodegenerative Diseases Technical University Munich Munich Germany

10. Geriatric Hospital Haag Haag Germany

Abstract

AbstractBackgroundBecause human fetal ventral mesencephalic tissue grafts provide promising results in ameliorating Parkinson's disease–implicated motor dysfunctions, human fetal midbrain‐derived dopamine neuronal precursor cells are considered good candidates for cell‐based therapy for Parkinson's disease in that large quantities of cells can be supplied through a good manufacturing practice–compliant system.ObjectiveWe conducted a prospective, phase I/IIa, dose‐escalation, open‐label “first‐in‐human” clinical trial with fetal neural precursor cells to assess their safety and therapeutic efficacy in patients with idiopathic Parkinson's disease.MethodsFifteen patients were assigned to receive three different doses of cells (4 × 106, 12 × 106, and 40 × 106 cells) and completed a 12‐month follow‐up. The primary outcome was safety, by measuring the presence of grade 3 or higher cells according to National Cancer Institute guidelines and any contaminated cells. Secondary outcomes assessed motor and neurocognitive function, as well as the level of dopamine transporters, by positron emission tomography–computed tomography.ResultsAlthough a pronation‐supination and hand/arm movement performance was remarkably enhanced in all three groups (all P < 0.05), the medium‐ and high‐dose‐treated groups exhibited significant improvement in Unified Parkinson's Disease Rating Scale Part III only up to 26.16% and 40%, respectively, at 12 months after transplantation without any serious clinical complications or graft‐induced dyskinesia in all patients. However, the motor improvements did not correlate with increase in the dopamine transporter on positron emission tomography images.ConclusionsOur results primarily demonstrate the safety and plausible dose‐dependent efficacy of human fetal midbrain‐derived dopamine neuronal precursor cells for idiopathic Parkinson's disease. © 2023 International Parkinson and Movement Disorder Society.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Fetal neural precursor cell treatment for PD;Nature Reviews Neurology;2023-02-07

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