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dc.contributor.authorMorizane, Asukaen
dc.contributor.alternative森實, 飛鳥ja
dc.date.accessioned2023-05-15T08:44:16Z-
dc.date.available2023-05-15T08:44:16Z-
dc.date.issued2023-02-27-
dc.identifier.urihttp://hdl.handle.net/2433/282095-
dc.description.abstractParkinson’s disease (PD) is the second most common neurodegenerative disease and a prime target of cell therapies. In fact, aborted fetal tissue has been used as donor material for such therapies since the 1980s. These cell therapies, however, suffer from several problems, such as a short supply of donor materials, quality instability of the tissues, and ethical restrictions. The advancement of stem cell technologies has enabled the production of donor cells from pluripotent stem cells with unlimited scale, stable quality, and less ethical problems. Several research groups have established protocols to induce dopamine neural progenitors from pluripotent stem cells in a clinically compatible manner and confirmed efficacy and safety in non-clinical studies. Based on the results from these non-clinical studies, several clinical trials of pluripotent stem cell-based therapies for PD have begun. In the context of immune rejection, there are several modes of stem cell-based therapies: autologous transplantation, allogeneic transplantation without human leukocyte antigen-matching, and allogeneic transplantation with matching. In this mini-review, several practical points of stem cell-based therapies for PD are discussed.en
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.publisherBMCen
dc.rights© The Author(s) 2023.en
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectPluripotent stem cellsen
dc.subjectParkinson's diseaseen
dc.subjectTransplantationen
dc.subjectCell therapyen
dc.subjectCentral nervous systemen
dc.titleCell therapy for Parkinson's disease with induced pluripotent stem cellsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleInflammation and Regenerationen
dc.identifier.volume43-
dc.relation.doi10.1186/s41232-023-00269-3-
dc.textversionpublisher-
dc.identifier.artnum16-
dc.identifier.pmid36843101-
dcterms.accessRightsopen access-
dc.identifier.eissn1880-8190-
出現コレクション:学術雑誌掲載論文等

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