• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

2022 Fiscal Year Final Research Report

Development of control method of immune response after multiple islet transplantation in anticipation of ES/iPS cell transplantation

Research Project

  • PDF
Project/Area Number 20K08999
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 55010:General surgery and pediatric surgery-related
Research InstitutionAichi Medical University

Principal Investigator

Ishiyama Kohei  愛知医科大学, 医学部, 准教授 (50437589)

Project Period (FY) 2020-04-01 – 2023-03-31
Keywords膵島移植 / 免疫制御 / 間葉系幹細胞
Outline of Final Research Achievements

To improve islet transplantation outcomes, we have begun developing immunoregulatory protocols using Stem cells from human exfoliated deciduous teeth (SHED), which have higher functional characteristics among Mesenchymal stem cells (MSC).
Unlike MSCs, which are easily affected by the cell culture environment, we have confirmed that SHEDs are a stable cell population. The ability to produce inhibitory factors was also significantly enhanced in SHED. Furthermore, we confirmed that SHED strongly suppressed human PBMC activation and cytotoxic activity to pancreatic islets. We confirmed that the PD1-PDL1 pathway is involved in this effect and that the immunosuppressive effect of MSC/SHD is not only mediated by humoral factors but also by cell-cell contact mechanisms.

Free Research Field

移植免疫

Academic Significance and Societal Importance of the Research Achievements

1型糖尿病に対する根治的治療法として死体ドナーからの同種膵島移植だけでなく、異種膵島やES/iPS細胞を用いた膵島移植にも期待がかかっている。しかしながら、移植医療普及のためには細胞移植治療効率を上げるための工夫が必要不可欠となる。免疫抑制効果を有するMSC/SHEDを用いることで膵島グラフト傷害が回避できる可能性について研究した。
本研究の結果、限られたグラフト提供を有効に活用するための治療戦略を開発することで、移植成績の向上、患者のQuality of life の改善、2型糖尿病への応用など臨床面だけでなく、医療費削減など経済面においても貢献ができると考える。

URL: 

Published: 2024-01-30  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi