Highlighted Paper selected by Editor-in-Chief : Secure Splenic Delivery of Plasmid DNA and Its Application to DNA Vaccine
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- Kurosaki Tomoaki
- Department of Hospital Pharmacy, Nagasaki University Hospital Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University
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- Kodama Yukinobu
- Department of Hospital Pharmacy, Nagasaki University Hospital
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- Muro Takahiro
- Department of Hospital Pharmacy, Nagasaki University Hospital
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- Higuchi Norihide
- Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University
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- Nakamura Tadahiro
- Department of Hospital Pharmacy, Nagasaki University Hospital
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- Kitahara Takashi
- Department of Hospital Pharmacy, Nagasaki University Hospital
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- Miyakoda Mana
- Division of Immunology, Department of Molecular Microbiology and Immunology, Graduate School of Biomedical Sciences, Nagasaki University
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- Yui Katsuyuki
- Division of Immunology, Department of Molecular Microbiology and Immunology, Graduate School of Biomedical Sciences, Nagasaki University
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- Sasaki Hitoshi
- Department of Hospital Pharmacy, Nagasaki University Hospital
書誌事項
- タイトル別名
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- Secure Splenic Delivery of Plasmid DNA and Its Application to DNA Vaccine
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抄録
In this experiment, we developed a novel safe and effective gene delivery vector coated with γ-polyglutamic acid (γ-PGA-coated complexes). The γ-PGA-coated complex was composed of chiseled spherical nano-particles with anionic charges. The plasmid DNA/polyethyleneimine complex (non-coated complex) showed high transgene efficiency in the spleen and lung after intravenous administration in mice, with high liver toxicity and lethality. On the other hand, γ-PGA-coated complex selectively showed high transgene efficiency in the spleen without such toxicity. Furthermore, the γ-PGA-coated complex highly accumulated and showed high gene expression in the marginal zone of the spleen. Those results strongly indicated that γ-PGA-coated complex was suitable as a DNA vaccine vector. We therefore applied γ-PGA-coated complex to melanoma DNA vaccine, pUb-M. The γ-PGA-coated complex containing pUb-M significantly inhibited the growth and metastasis of a melanoma cell line, B16-F10 cells. In conclusion, we developed a splenic gene vector, γ-PGA-coated complex, as a novel technology for clinical vaccination.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 36 (11), 1800-1806, 2013
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204634318976
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- NII論文ID
- 130003382044
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- NII書誌ID
- AA10885497
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- COI
- 1:STN:280:DC%2BC2c7ivFymsw%3D%3D
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- ISSN
- 13475215
- 09186158
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- HANDLE
- 10069/34047
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- NDL書誌ID
- 024957810
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- PubMed
- 24189423
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- IRDB
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可