» Articles » PMID: 33490319

IPS Cell-based Therapy for Parkinson's Disease: A Kyoto Trial

Overview
Journal Regen Ther
Date 2021 Jan 25
PMID 33490319
Citations 72
Authors
Affiliations
Soon will be listed here.
Abstract

Following intensive efforts since their discovery little more than 10 years ago, cell replacement therapy using induced pluripotent stem (iPS) cells is now becoming reality. However, there remain several obstacles in the translation of basic research to clinical application, obstacles known as the "Valley of Death". With regards to regenerative medicine using iPS cells for Parkinson's disease, we have developed a method for the 1) efficient induction of dopaminergic neurons from human iPS cells and 2) sorting dopaminergic progenitor cells using a floor plate marker, CORIN. The grafted CORIN cells survived well and functioned as midbrain dopaminergic neurons in the Parkinson's disease model rats and monkeys, and showed minimal risk of tumor formation. Based on these results, we performed a pre-clinical study using a clinical-grade iPS cell line and finally started a clinical trial to treat Parkinson's disease patients in August 2018. Here, I discuss the key issues to crossing the Valley of Death: scientific rationale, pre-clinical study, and clinical trial.

Citing Articles

Relationship Between Location of Cell Transplantation and Recovery for Intracerebral Stem Cell Transplantation for Chronic Traumatic Brain Injury: Analysis of STEMTRA Trial.

Kawabori M, Karasawa Y, Suenaga J, Nakamura H, Imai H, Yasuhara T Neurotrauma Rep. 2025; 6(1):106-114.

PMID: 39990703 PMC: 11839542. DOI: 10.1089/neur.2024.0130.


Mapping the global clinical landscape of stem cell therapies for neurological diseases from 1998 to 2023: an analysis based on the Trialtrove database.

Jiang S, Bao X, Zhong C, Wang R Stem Cell Res Ther. 2025; 16(1):41.

PMID: 39901212 PMC: 11792730. DOI: 10.1186/s13287-024-04096-2.


Research of reprogramming toward clinical applications in regenerative medicine: A concise review.

Nakatsukasa Y, Yamada Y, Yamada Y Regen Ther. 2024; 28:12-19.

PMID: 39678397 PMC: 11638634. DOI: 10.1016/j.reth.2024.11.008.


The Abnormal Proliferation of Midbrain Dopamine Cells From Human Pluripotent Stem Cells Is Induced by Exposure to the Tumor Microenvironment.

Xue J, Wu D, Bao Y, Wu Y, Zhang X, Chen L CNS Neurosci Ther. 2024; 30(11):e70117.

PMID: 39563017 PMC: 11576488. DOI: 10.1111/cns.70117.


Human iPSC-derived neural stem cells displaying radial glia signature exhibit long-term safety in mice.

Luciani M, Garsia C, Beretta S, Cifola I, Peano C, Merelli I Nat Commun. 2024; 15(1):9433.

PMID: 39487141 PMC: 11530573. DOI: 10.1038/s41467-024-53613-7.


References
1.
Chambers S, Fasano C, Papapetrou E, Tomishima M, Sadelain M, Studer L . Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling. Nat Biotechnol. 2009; 27(3):275-80. PMC: 2756723. DOI: 10.1038/nbt.1529. View

2.
Doi D, Morizane A, Kikuchi T, Onoe H, Hayashi T, Kawasaki T . Prolonged maturation culture favors a reduction in the tumorigenicity and the dopaminergic function of human ESC-derived neural cells in a primate model of Parkinson's disease. Stem Cells. 2012; 30(5):935-45. DOI: 10.1002/stem.1060. View

3.
Doi D, Magotani H, Kikuchi T, Ikeda M, Hiramatsu S, Yoshida K . Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson's disease. Nat Commun. 2020; 11(1):3369. PMC: 7338530. DOI: 10.1038/s41467-020-17165-w. View

4.
Katsukawa M, Nakajima Y, Fukumoto A, Doi D, Takahashi J . Fail-Safe Therapy by Gamma-Ray Irradiation Against Tumor Formation by Human-Induced Pluripotent Stem Cell-Derived Neural Progenitors. Stem Cells Dev. 2016; 25(11):815-25. DOI: 10.1089/scd.2015.0394. View

5.
Xi J, Liu Y, Liu H, Chen H, Emborg M, Zhang S . Specification of midbrain dopamine neurons from primate pluripotent stem cells. Stem Cells. 2012; 30(8):1655-63. PMC: 3405174. DOI: 10.1002/stem.1152. View