| Project/Area Number |
21790387
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Experimental pathology
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| Research Institution | Kyushu University |
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Principal Investigator |
INOUE Hiroyuki Kyushu University, 生体防御医学研究所, 助教 (80529967)
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| Project Period (FY) |
2009 – 2010
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| Project Status |
Completed (Fiscal Year 2010)
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| Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2010: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2009: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
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| Keywords | 腫瘍免疫 / メモリーT細胞 / BLT1 / LTB4 / GM-CSF / GVAX |
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| Research Abstract |
In this study, we successfully identified CD4+T cells as a pivotal determinant responsible for developing long-term antitumor effect during re-rejection of rechallenge of WEHI3B cells, a mouse monocytic leukemia cell line, after observation of marked rejection of in vivo s.c. administration of GM-CSF gene transduced WEHI3B (WGM) cells. In addition, ratios of various memory CD4+T cells including stem central memory CD4+T and CD8+ T cells in lymph nodes (LNs) collected at day 46 were increased in BLT1 mice inoculated with WGM cells. As a prospective mechanism, our immunological findings suggest that absence of LTB4/BLT1 signaling facilitates effective and sustained generation of potent tumor associated antigens (TAAs) specific memory CD4+T cells by promoting activation of mature DCs in LNs and migration of TAAs phagocytosed DCs into LNs, subsequently leading to augmented adaptive immunities (Th1 and Th2 cells) and repressing a wide range of regulatory CD4+ T cells known to hinder antitumor immunity.
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