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

2020 Fiscal Year Final Research Report

Development of NK Cell expansion by a novel membrane-bound chimeric cytokine

Research Project

  • PDF
Project/Area Number 18K07259
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 50020:Tumor diagnostics and therapeutics-related
Research InstitutionNiigata University

Principal Investigator

Imamura Masaru  新潟大学, 医歯学総合病院, 講師 (80464006)

Co-Investigator(Kenkyū-buntansha) 今井 千速  新潟大学, 医歯学系, 准教授 (90419284)
Project Period (FY) 2018-04-01 – 2021-03-31
Keywords膜結合型サイトカイン / 細胞療法 / NK細胞
Outline of Final Research Achievements

The purpose of this study is to develop membrane-bound chimeric cytokines to increase NK cells without systemic administration of cytokines that may cause side effects and to realize safe and effective NK cell therapy. First, we generated the construct of hybrid membrane-bound interleukins 15 and 21. Next, we transduced the construct into a tumor cell line, K562 necessary for the expansion of NK cells, and the efficiency of transduction was as high as 85.5%. When we examined the expansion of NK cells transfected with the construct, we found that the expansion was 27-fold after 7 days, but not as expected.

Free Research Field

小児血液腫瘍

Academic Significance and Societal Importance of the Research Achievements

膜結合型サイトカインはサイトカイン分泌を伴わないため全身投与より安全と考えられる。サイトカインの種類及び構造の最適化によりNK細胞を効率的に増やすことができ、安全で効果的な新規NK細胞療法の実現が可能になると考えられる。今回新しく開発したIL-15とIL-21のハイブリッド膜結合型サイトカインはNK細胞を十分に増やす効果は得られず、新たな工夫が必要と考えられた。

URL: 

Published: 2022-01-27  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi