WO2008133206A1 - Vecteur de virus de paramyxoviridae non répliquant - Google Patents
Vecteur de virus de paramyxoviridae non répliquant Download PDFInfo
- Publication number
- WO2008133206A1 WO2008133206A1 PCT/JP2008/057609 JP2008057609W WO2008133206A1 WO 2008133206 A1 WO2008133206 A1 WO 2008133206A1 JP 2008057609 W JP2008057609 W JP 2008057609W WO 2008133206 A1 WO2008133206 A1 WO 2008133206A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- gene
- vector
- replicating
- sev
- cell
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N7/00—Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
- C12N15/86—Viral vectors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/60—Fusion polypeptide containing spectroscopic/fluorescent detection, e.g. green fluorescent protein [GFP]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/61—Fusion polypeptide containing an enzyme fusion for detection (lacZ, luciferase)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10041—Use of virus, viral particle or viral elements as a vector
- C12N2710/10043—Use of virus, viral particle or viral elements as a vector viral genome or elements thereof as genetic vector
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2760/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses negative-sense
- C12N2760/00011—Details
- C12N2760/18011—Paramyxoviridae
- C12N2760/18811—Sendai virus
- C12N2760/18851—Methods of production or purification of viral material
- C12N2760/18852—Methods of production or purification of viral material relating to complementing cells and packaging systems for producing virus or viral particles
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2800/00—Nucleic acids vectors
- C12N2800/30—Vector systems comprising sequences for excision in presence of a recombinase, e.g. loxP or FRT
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- General Health & Medical Sciences (AREA)
- Microbiology (AREA)
- Virology (AREA)
- Biochemistry (AREA)
- Plant Pathology (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Immunology (AREA)
- Medicinal Chemistry (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Un vecteur SeV non répliquant (vecteur SeV/ΔP) peut être produit avec succès, lequel présente la délétion d'un gène pour la protéine P qui est une protéine constituant un RNP à partir de l'ARN génomique ou l'inactivation du gène. Il a été trouvé qu'un vecteur SeV qui a la délétion ou l'inactivation du gène P et porte un gène marqueur tel qu'un gène pour la GFP ou la luciférase peut être utilisé pour parvenir à un rendement de transfert élevé d'un gène étranger dans une cellule ou un rendement d'expression élevé d'un gène étranger dans une cellule. Il a également été découvert que le vecteur a une cytotoxicité réduite parce que le gène P est délété ou inactivé dans le vecteur pour provoquer la réduction de la quantité d'une protéine d'origine virale, exprimée dans une cellule hôte.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007110547 | 2007-04-19 | ||
| JP2007-110547 | 2007-04-19 | ||
| JP2007-127421 | 2007-05-11 | ||
| JP2007127421 | 2007-05-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2008133206A1 true WO2008133206A1 (fr) | 2008-11-06 |
Family
ID=39925660
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2008/057609 Ceased WO2008133206A1 (fr) | 2007-04-19 | 2008-04-18 | Vecteur de virus de paramyxoviridae non répliquant |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2008133206A1 (fr) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010008054A1 (fr) * | 2008-07-16 | 2010-01-21 | ディナベック株式会社 | Procédé de fabrication d'une cellule reprogrammée utilisant un vecteur viral chromosomiquement non intégré |
| WO2016125364A1 (fr) * | 2015-02-02 | 2016-08-11 | 株式会社Idファーマ | Vecteur viral à arn de polarité négative amélioré |
| US12252700B2 (en) | 2015-11-13 | 2025-03-18 | Id Pharma Co., Ltd. | Paramyxovirus vector |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005065596A (ja) * | 2003-08-25 | 2005-03-17 | Japan Science & Technology Agency | 増殖能欠損狂犬病ウイルス |
| WO2007007921A1 (fr) * | 2005-07-13 | 2007-01-18 | Kyushu University, National University Corporation | Vecteur de mononégavirus recombinant de type génome fractionné |
-
2008
- 2008-04-18 WO PCT/JP2008/057609 patent/WO2008133206A1/fr not_active Ceased
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005065596A (ja) * | 2003-08-25 | 2005-03-17 | Japan Science & Technology Agency | 増殖能欠損狂犬病ウイルス |
| WO2007007921A1 (fr) * | 2005-07-13 | 2007-01-18 | Kyushu University, National University Corporation | Vecteur de mononégavirus recombinant de type génome fractionné |
Non-Patent Citations (4)
| Title |
|---|
| HANAZONO Y.: "Shinki Sendai Virus Vector o Mochiita Saitaiketsu Kansaibo Zofukuho no Kaihatsu", SHINKI SENDAI VIRUS VECTOR O MOCHIITA SAITAIKETSU KANSAIBO ZOFUKUHO NO KAIHATSU HEISEI 18 NENDO SOKATSU. BUNTAN KENKYU HOKOKUSHO, March 2007 (2007-03-01), pages 1 - 7 * |
| INOUE M.: "HoxB4 Idenshi o Tosao suru P Kessongata SeV Vector no Sakusei to Seino Hyoka ni Kansuru Kenkyu", SHINKI SENDAI VIRUS VECTOR O MOCHIITA SAITAIKETSU KANSAIBO ZOFUKUHO NO KAIHATSU HEISEI 18 NENDO SOKATSU. BUNTAN KENKYU HOKOKUSHO, March 2007 (2007-03-01), pages 8 - 11 * |
| MORIMOTO K.: "Virus Vector o Oyo shita Vaccine Kaihatsu Jinsokuka no Tameno Kibanteki Gijutsu Kaihatsu no Kenkyu", VIRUS VECTOR O OYO SHITA VACCINE KAIHATSU JINSOKUKA NO TAMENO KIBANTEKI GIJUTSU KAIHATSU NO KENKYU HEISEI 17 NENDO SOKATSU. BUNTAN KENKYU HOKOKUSHO, 2006, pages 1 - 15 * |
| WIEGAND M.A. ET AL.: "De novo synthesis of N and P proteins as a key step in Sendai virus gene expression", J. VIROL., vol. 81, no. 24, pages 13835 - 13844, XP002684869, DOI: doi:10.1128/JVI.00914-07 * |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010008054A1 (fr) * | 2008-07-16 | 2010-01-21 | ディナベック株式会社 | Procédé de fabrication d'une cellule reprogrammée utilisant un vecteur viral chromosomiquement non intégré |
| US9127256B2 (en) | 2008-07-16 | 2015-09-08 | Dnavec Corporation | Method for production of reprogrammed cell using chromosomally unintegrated virus vector |
| US9695445B2 (en) | 2008-07-16 | 2017-07-04 | Id Pharma Co., Ltd. | Method for production of reprogrammed cell using chromosomally unintegrated virus vector |
| US11136594B2 (en) | 2008-07-16 | 2021-10-05 | Id Pharma Co., Ltd. | Method for production of reprogrammed cell using chromosomally unintegrated virus vector |
| WO2016125364A1 (fr) * | 2015-02-02 | 2016-08-11 | 株式会社Idファーマ | Vecteur viral à arn de polarité négative amélioré |
| JPWO2016125364A1 (ja) * | 2015-02-02 | 2017-11-30 | 株式会社Idファーマ | 改良されたマイナス鎖rnaウイルスベクター |
| JP2020195381A (ja) * | 2015-02-02 | 2020-12-10 | 株式会社Idファーマ | 改良されたマイナス鎖rnaウイルスベクター |
| US12252700B2 (en) | 2015-11-13 | 2025-03-18 | Id Pharma Co., Ltd. | Paramyxovirus vector |
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