『徳島大学 教育・研究者情報データベース (EDB)』---[学外] /
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種別 (必須): 学術論文 (審査論文) [継承]
言語 (必須): 英語 [継承]
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著者 (必須): 1. (英) Hasegawa K (日) (読)
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2. (英) Tagawa M (日) (読)
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3. (英) Takagi K (日) (読)
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4. (英) Tsukamoto H (日) (読)
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5. (英) Tomioka Y (日) (読)
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6. (英) Suzuki T (日) (読)
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7.西岡 安彦 ([徳島大学.大学院医歯薬学研究部.医学域.医科学部門.内科系.呼吸器・膠原病内科学])
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8. (英) Ohrui T (日) (読)
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9. (英) Numasaki M (日) (読)
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題名 (必須): (英) Anti-tumor immunity elicited by direct intratumoral administration of a recombinant adenovirus expressing either IL-28A/IFN-λ2 or IL-29/IFN-λ1.  (日)    [継承]
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要約 (任意): (英) Interleukin (IL)-28A/interferon (IFN)-λ2 and IL-29/IFN-λ1 have been demonstrated to elicit direct and indirect anti-tumor actions. In this study, we constructed an adenovirus vector expressing either IL-28A/IFN-λ2 (AdIL-28A) or IL-29/IFN-λ1 (AdIL-29) to evaluate the therapeutic properties of intratumoral injection of recombinant adenovirus to apply for the clinical implementation of cancer gene therapy. Despite the lack of an anti-proliferative effect on MCA205 and B16-F10 cells, a retarded growth of established subcutaneous tumors was observed following multiple injections of either AdIL-28A or AdIL-29 when compared with AdNull. In vivo cell depletion experiments displayed that both NK cells and CD8(+) T cells have a major role in AdIL-28A-mediated tumor growth suppression. A significant increase in the number of infiltrating CD8(+) T cells into the tumors treated with either AdIL-28A or AdIL-29 was observed. Moreover, specific anti-tumor cytotoxic T lymphocyte reactivity was detected in spleen cells from animals treated with either AdIL-28A or AdIL-29. In IFN-γ-deficient mice, anti-tumor activities of AdIL-28A were completely impaired, indicating that IFN-γ is critically involved in the tumor growth inhibition triggered by AdIL-28A. IL-12 provided a synergistic anti-tumor effect when combined with AdIL-28A. These results indicate that AdIL-28A and AdIL-29 could be successfully utilized as an alternative cancer immunogene therapy.  (日)    [継承]
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誌名 (必須): Cancer Gene Therapy ([Nature Publishing Group])
(pISSN: 0929-1903, eISSN: 1476-5500)

ISSN (任意): 1476-5500
ISSN: 0929-1903 (pISSN: 0929-1903, eISSN: 1476-5500)
Title: Cancer gene therapy
Title(ISO): Cancer Gene Ther
Publisher: Springer Nature
 (NLM Catalog  (Scopus  (CrossRef (Scopus information is found. [need login])
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年月日 (必須): 西暦 2016年 8月 19日 (平成 28年 8月 19日) [継承]
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DOI (任意): 10.1038/cgt.2016.29    (→Scopusで検索) [継承]
PMID (任意): 27561689    (→Scopusで検索) [継承]
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備考 (任意): 1.(英) Article.ELocationID: 10.1038/cgt.2016.29  (日)    [継承]
2.(英) Article.PublicationTypeList.PublicationType: Journal Article  (日)    [継承]

標準的な表示

和文冊子 ● K Hasegawa, M Tagawa, K Takagi, H Tsukamoto, Y Tomioka, T Suzuki, Yasuhiko Nishioka, T Ohrui and M Numasaki : Anti-tumor immunity elicited by direct intratumoral administration of a recombinant adenovirus expressing either IL-28A/IFN-λ2 or IL-29/IFN-λ1., Cancer Gene Therapy, 23, 8, 266-277, 2016.
欧文冊子 ● K Hasegawa, M Tagawa, K Takagi, H Tsukamoto, Y Tomioka, T Suzuki, Yasuhiko Nishioka, T Ohrui and M Numasaki : Anti-tumor immunity elicited by direct intratumoral administration of a recombinant adenovirus expressing either IL-28A/IFN-λ2 or IL-29/IFN-λ1., Cancer Gene Therapy, 23, 8, 266-277, 2016.

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