Development of effective immunotherapy by combining methods to restore immunocompetence of cancer patients
Project/Area Number |
19390355
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Digestive surgery
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Research Institution | Keio University |
Principal Investigator |
KAWAKAMI Yutaka Keio University, 医学部, 教授 (50161287)
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Co-Investigator(Kenkyū-buntansha) |
KITAGAWA Yuukou 慶應義塾大学, 医学部, 教授 (20204878)
FUJITA Tomonobu 慶應義塾大学, 医学部, 助教 (20199334)
SAKURAI Toshiharu 慶應義塾大学, 医学部, 助教 (20101933)
TSUKAMOTO Nobuo 慶應義塾大学, 医学部, 助教 (20407117)
KUDO Chie 慶應義塾大学, 医学部, 助教 (90424126)
SUMIMOTO Hidetoshi 慶應義塾大学, 医学部, 助教 (00306838)
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Project Period (FY) |
2007 – 2008
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Project Status |
Completed (Fiscal Year 2008)
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Budget Amount *help |
¥18,980,000 (Direct Cost: ¥14,600,000、Indirect Cost: ¥4,380,000)
Fiscal Year 2008: ¥7,150,000 (Direct Cost: ¥5,500,000、Indirect Cost: ¥1,650,000)
Fiscal Year 2007: ¥11,830,000 (Direct Cost: ¥9,100,000、Indirect Cost: ¥2,730,000)
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Keywords | 大腸癌 / 免疫療法 / 免疫抑制 / 樹状細胞 / シグナル伝達阻害 / 上皮間葉転換 / 消化器癌 / 膵癌 / 腫瘍抗原 / 癌遺伝子 / RNA干渉 |
Research Abstract |
本研究では、効果的な免疫療法の開発のために、消化器癌による免疫抑制の分子機構の解明と克服法の開発、および免疫療法の標的となるヒト消化器癌抗原の同定を試みた。その結果、発現と良好な予後との相関がみられ、免疫原性の高い腫瘍抗原が同定され、さらに、大腸癌シグナル異常による免疫抑制機構が明らかになり、in vitroおよび大腸癌マウスモデルで、シグナル阻害による免疫抑制の解除と免疫療法の効果増強の可能性が示された。
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Report
(3 results)
Research Products
(98 results)
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[Journal Article] A Pilot Study of Human Interferon β Gene Therapy for Patients with Advanced Melanoma by in vivo Transduction Using Cationic Liposomes2008
Author(s)
Matsumoto K, Kubo H, Murata H, Uhara H, Takata M, Shinichi Shibata S, Yasue S, Sakakibara A, Yasushi TomitaY, Toshiro Kageshita T, Kawakami Y, Mizuno M, Yoshida J and Saida T.
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Journal Title
Jpn J Clin Oncol 38
Pages: 849-856
Related Report
Peer Reviewed
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[Journal Article] Identification of a WT1 protein-derived peptide, WT1, as a HLA-A 0206-restricted, WT1-specific CTL epitope2008
Author(s)
Li Z, Oka Y, Tsuboi A, Fujiki F, Harada Y, Nakajima H, Masuda T, Fukuda Y, Kawakatsu M, Morimoto S, Katagiri T, Tatsumi N, Hosenn N, Shirakata T, Nishida S, Kawakami Y, Udaka K, Kawase I, Oji Y, Sugiyama H.
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Journal Title
Microbiol Immunol 52
Pages: 551-558
Related Report
Peer Reviewed
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[Journal Article] Isolation and characterization of dendritic cells from common marmosets for preclinical studies on cell therapy2008
Author(s)
Ohta S, Ueda Y, Yaguchi M, Matsuzaki Y, Nakamura M, Toyama Y, Tanioka Y, Tamaoki N, Nomura T, Okano H, Kawakami Y, Toda M.
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Journal Title
Immunol 123
Pages: 566-574
Related Report
Peer Reviewed
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[Journal Article] Dendritic cell based personalized immunotherapy based on cancer antigen research2008
Author(s)
Kawakami Y, Fujita T, Kudo C, Sakurai T, Udagawa M, Yaguchi T, Hasegawa G, Hayashi E, Ueda Y, Iwata T, Wang Q, Okada S, Tsukamoto N, Matsuzaki Y, Sumimoto H.
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Journal Title
Frontier in Bioscience 13
Pages: 1952-1958
Related Report
Peer Reviewed
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[Journal Article] Development of individualized immunotherapy based on the analysis on anti-tumor immune responses to the human tumor antigens identified using immunological and genetic methods2007
Author(s)
Kawakami Y, Fujita T, Kudo C, Sakurai T, Udagawa M, Hasegawa G, Ishida A, Kitagawa Y, Tanabe M, Saito M, Izumi Y, Kawamura M, Yaguchi T, Ueda Y, Hayashi E, Wang Q, Tsukamoto N, Matsuzaki Y, Sumimoto H, Takeuchi H, Tanikawa A, Handa M, Amagai M, Kobayashi K, Ikeda Y, Azuma I, and Kitajima M.
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Journal Title
Gene Therapy
Pages: 240-248
Related Report
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[Presentation] 癌細胞におけるMAPKシグナル亢進による腫瘍免疫逃避機構の解明2008
Author(s)
谷口智憲, 木藤健治, 塚本信夫, 桜井敏晴, 藤田知信, 持丸博史, 丸山正太郎, 里見良輔, 井田陽介, 住本秀敏, 河上裕
Organizer
第38回日本免疫学会
Place of Presentation
国立京都国際会館
Year and Date
2008-12-02
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[Presentation] 培養樹状細胞を用いた免疫療法2008
Author(s)
河上裕, 住本秀敏, 工藤千恵, 塚本信夫, 藤田知信, 桜井敏晴, 谷口智憲, 岩田知子, 川村直
Organizer
第67回日本癌学会学術総会
Place of Presentation
名古屋国際会議場
Year and Date
2008-10-28
Related Report
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[Presentation] 胃癌細胞株の幹細胞におけるMyeloid cell Leukemia-l(Mcl-l)蛋白阻害によるアポトーシス増強作用の検討2008
Author(s)
飯塚秀子, 樋口肇, 住本秀敏, 樺島彩乃, 酒井元, 泉谷幹子, 山岸由幸, 高石官均, 河上裕, 水口裕之, 日比紀之
Organizer
第67回日本癌学会学術総会
Place of Presentation
名古屋国際会議場
Year and Date
2008-10-28
Related Report
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