| Project/Area Number |
16591255
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
General surgery
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| Research Institution | Okayama University |
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Principal Investigator |
YAGI Takahito Okayama University Medical and Dental Hospital, Lecturer, 医学部・歯学部附属病院, 助手 (00304353)
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| Co-Investigator(Kenkyū-buntansha) |
SADAMORI Hiroshi Okayama University Medical and Dental Hospital, Assistant Professor, 医学部・歯学部附属病院, 助手 (30362974)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2005: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2004: ¥2,300,000 (Direct Cost: ¥2,300,000)
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| Keywords | Small bowel transplantation / donor specific hyporesponsiveness / bone marrow transplantation / portal injection / dendritic cell / 拒絶反応 / 骨髄細胞 / グラフト潤滑リンパ球 / サイトカインバランス / 骨髄由来樹状細胞 |
|---|
| Research Abstract |
We have been reported that bone marrow cells were stronger effector cells than peripheral mononuclear cells in induction of donor specific hyporesponsiveness. And portal injection as administration route of donor antibody was more efficient than peripheral vessels with a small bowel transplantation (SBT) model. Even bone marrow transplantation (BMT) was given at the same time with the transplant surgery of SBT in the portal vein, induction efficiency didn't decrease, and the presensitization which obstructed transplantation was not caused. In order to increase the efficiency of the peculiar immune suppression acquisition by BMT with a rat SBT model, we planned bone marrow dendritic cell isolation, cultivation, maturation control and transplant experiments. It was confirmed that the main population of the induction of donor specific hyporesponsiveness was immature dendritic cell in the DAYO transportal BMT in SBT. And, though treatment by the immature dendritic cell significantly prolonged the graft survival of the rat SBT, it was found out that fatal GVHD was made to occur in BMT with the mature cell, and further examination could be necessary to the maintenance of a differentiation of cultured dendritic cell in the safer clinical application.
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