Development of a novel antileukemia adoptive immunotherapy using leukemia-reactive gene-modified memory T cells.
Project/Area Number |
24591426
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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 |
Hematology
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Research Institution | Ehime University |
Principal Investigator |
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Project Period (FY) |
2012-04-01 – 2015-03-31
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Project Status |
Completed (Fiscal Year 2014)
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Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2012: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
|
Keywords | 遺伝子細胞免疫療法 / T細胞受容体(TCR)遺伝子 / 遺伝子改変Tリンパ球 / 免疫記憶細胞 / 白血病幹細胞 / 細胞傷害性Tリンパ球(CTL) / T細胞受容体遺伝子(TCR)遺伝子 / 抗白血病効果 / 白血病性幹細胞 / 細胞免疫療法 |
Outline of Final Research Achievements |
The clinical efficacy mediated by gene-modified CD8+ T-lymphocytes using leukemia antigen-specific T-cell receptor (TCR) gene transfer (artificial cytotoxic T lymphocytes: artificial CTL) depends on the in vivo persistence of those artificial CTL after recognition of leukemia cells. In this study, to this end, we assessed the helper function mediated by newly gene-modified CD4+ T-lymphocytes (artificial helper T cells) using the identical HLA class I-restricted TCR gene which was employed for artificial CTLs. In results, those artificial helper T cells successfully stimulated artificial CTLs to survive longer after recognition of leukemia cells in vivo through the facilitation of memory T-cell formation mediated by artificial CTL.
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Report
(4 results)
Research Products
(91 results)
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[Journal Article] Antileukemia multifunctionality of CD4+ T cells genetically engineered by HLA class I-restricted and WT1-specific T-cell receptor gene transfer.2015
Author(s)
Fujiwara H*, Ochi T, Ochi F, Miyazaki Y, Asai H, Narita M, Okamoto S, Mineno J, Kuzushima K, Shiku H, Yasukawa M.
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Journal Title
Related Report
Peer Reviewed
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[Journal Article] Dose-intensified chemotherapy alone or in combination with mogamulizumab in newly diagnosed aggressive adult T-cell leukaemia-lymphoma: a randomized phase II study.2015
Author(s)
Ishida T, Jo T, Takemoto S, Suzushima H, Uozumi K, Yamamoto K, Uike N, Saburi Y, Nosaka K, Utsunomiya A, Tobinai K, Fujiwara H, Ishitsuka K, Yoshida S, Taira N, Moriuchi Y, Imada K, Miyamoto T, Akinaga S, Tomonaga M, Ueda R
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Journal Title
Br J Haematol
Volume: 未定
Issue: 5
Pages: 672-682
DOI
Related Report
Peer Reviewed
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[Journal Article] Adoptive transfer of genetically engineered WT1-specific cytotoxic T lymphocytes does not induce renal injury2014
Author(s)
Asai H, Fujiwara H, Kitazawa S, Kobayashi N, Ochi T, Miyazaki Y, Ochi F, Akatsuka Y, Okamoto S, Mineno J, Kuzushima K, Ikeda H, Shiku H, Yasukawa M
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Journal Title
J Hematol Oncol.
Volume: 7
Issue: 1
Pages: 3-3
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Adoptive transfer of genetically modified Wilms' tumor 1-specific T cells in a novel malignant skull base meningioma model.2013
Author(s)
Iwami K, Natsume A, Ohno M, Ikeda H, Mineno J, Nukaya I, Okamoto S, Fujiwara H, Yasukawa M, Shiku H, Wakabayashi T.
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Journal Title
Neuro Oncol.
Volume: 15
Issue: 6
Pages: 747-758
DOI
Related Report
Peer Reviewed
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[Presentation] 移植と抗腫瘍免疫療法2015
Author(s)
藤原 弘*
Organizer
第37回 日本造血細胞移植学会総会 教育講演3
Place of Presentation
神戸市
Year and Date
2015-03-05 – 2015-03-07
Related Report
Invited
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[Presentation] Concomitant administration of gene-modified T cells expressing a chimeric CD16-CD3zeta receptor with Mogamulizmab synergistically suppresses adult T cell leukemia cells in vivo.2014
Author(s)
Tanimoto K, Fujiwara H*, Tanaka H, Ochi F, Asai H, Okamoto S, Mineno J, Kuzushima K, Shiku H, Barrett AJ, Yasukawa M.
Organizer
56th American Society of Hematology, Annual meeting and Exposition
Place of Presentation
San Francisco, CA
Year and Date
2014-12-06 – 2014-12-09
Related Report
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