Project/Area Number |
16591901
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Pathobiological dentistry/Dental radiology
|
Research Institution | Fukuoka Dental College |
Principal Investigator |
OHNO JUN Fukuoka Dental College, Lecturer, 歯学部, 講師 (10152208)
|
Project Period (FY) |
2004 – 2006
|
Project Status |
Completed (Fiscal Year 2006)
|
Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2005: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2004: ¥1,300,000 (Direct Cost: ¥1,300,000)
|
Keywords | GVT / ICAM-1 / CTL / Melanoma / sialic acid / Dendritic cell / tumor immunology / ICAM-1 / 口腔がん / がん免疫 / GVHD / がんワクチン療法 / 悪性黒色腫 / 免疫組織化学 / マウス |
Research Abstract |
Graft-versus-tumor, GVT, is one of cellular immunotherapies for malignant tumors. In this study, we examined the effect of cytotoxic T cells (CTLs) presented melanoma antigens by dendritic cell (DC) to melanoma cell which have expressed intercellular adhesion molecule-1 (ICAM-1). Matured DCs were pulsed by a solution of B16 (melanoma cells) cells. CD8-positive T cells (CTLs) were stimulated by the co-culture of matured and pulsed DCs. After those procudures, the CTLs must be reactive with melanoma cells in vivo. As B16 cells were cultured in DMEM medium with interferon-gamma (IFN-g), those cells expressed ICAM-1 on the cell surface. The mouse melanoma model was made by the injection of B16 cell expressed ICAM-1 into the tongue. The controls were prepared as 1) the injection of DMEM insted of the B16 cell-injection, and 2) the injection of B16 cells without the expression with ICAM-1. The tongue with the injcetion of ICAM-1-B16 cells revealed remakable reduction of tumor growth, compared with the controls. These results suggested that the GVT, with combination of pulsed DCs and ICAM-1 expression on tumor cells, may be increased effects of tumor immunotherapy.
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