Elucidation of the pathogenesis of inflammatory bowel disease based on selective IL-17F regulation via Dectin-1.
Project/Area Number |
26460966
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Gastroenterology
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Research Institution | Shiga University of Medical Science |
Principal Investigator |
Ban Hiromitsu 滋賀医科大学, 医学部, 特任助教 (30598363)
|
Co-Investigator(Kenkyū-buntansha) |
馬場 重樹 滋賀医科大学, 医学部, 助教 (40422901)
|
Project Period (FY) |
2014-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2016: ¥520,000 (Direct Cost: ¥400,000、Indirect Cost: ¥120,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
|
Keywords | 炎症性腸疾患 / サイトカイン / アンチセンスオリゴ / Interleukin-17 / DSS腸炎マウス / インターロイキン / 炎症性サイトカイン / 腸炎モデルマウス / 抗炎症作用 |
Outline of Final Research Achievements |
IL-17β is highly expressed from Dectin-1 positive cells with IL-1β. In addition, we have studied the introduction of antisense DNA nucleotide sequences into cells using β-1,3-D-gulcan, Schizophyllan as a carrier, in a Dectin-1 dependent manner. Based on these two studies, IL-17F highly expressed from Dectin-1 positive cells in intestinal inflammation model mice was suppressed by intracellular introduction of antisense DNA by using SPG-mediated Drug delivery system We will elucidate the role of IL-17F expressed from Dectin-1 positive cells and aim to develop new therapeutic agents for inflammatory bowel disease.
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Report
(4 results)
Research Products
(5 results)
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[Journal Article] Prognostic factors affecting early colectomy in patients with moderate to severe ulcerative colitis treated with calcineurin inhibitors.2016
Author(s)
Ban H, Bamba S, Nishida A, Inatomi O, Shioya M, Takahashi KI, Imaeda H, Murata M, Sasaki M, Tsujikawa T, Andoh A.
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Journal Title
Exp Ther Med.
Volume: 12
Pages: 829-834
Related Report
Peer Reviewed / Acknowledgement Compliant