DK2350268T3 - Fremgangsmåde til produktion af adenovirusvektorer - Google Patents

Fremgangsmåde til produktion af adenovirusvektorer Download PDF

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Publication number
DK2350268T3
DK2350268T3 DK09744140.6T DK09744140T DK2350268T3 DK 2350268 T3 DK2350268 T3 DK 2350268T3 DK 09744140 T DK09744140 T DK 09744140T DK 2350268 T3 DK2350268 T3 DK 2350268T3
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cells
cell
rad35
bioreactor
adenovirus
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DK09744140.6T
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Alfred Luitjens
John Alfred Lewis
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Crucell Holland Bv
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/02Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N7/00Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M3/00Tissue, human, animal or plant cell, or virus culture apparatus
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2710/00MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
    • C12N2710/00011Details
    • C12N2710/10011Adenoviridae
    • C12N2710/10311Mastadenovirus, e.g. human or simian adenoviruses
    • C12N2710/10341Use of virus, viral particle or viral elements as a vector
    • C12N2710/10343Use of virus, viral particle or viral elements as a vector viral genome or elements thereof as genetic vector
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2710/00MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
    • C12N2710/00011Details
    • C12N2710/10011Adenoviridae
    • C12N2710/10311Mastadenovirus, e.g. human or simian adenoviruses
    • C12N2710/10351Methods of production or purification of viral material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
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  • Organic Chemistry (AREA)
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  • Genetics & Genomics (AREA)
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  • Microbiology (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Virology (AREA)
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  • Proteomics, Peptides & Aminoacids (AREA)
  • Physics & Mathematics (AREA)
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  • Molecular Biology (AREA)
  • Cell Biology (AREA)
  • Sustainable Development (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)

Claims (7)

1. Fremgangsmåde til produktion af rekombinant adenovirus serotype 35 (rAd35) i en bioreaktor, hvilken fremgangsmåde omfatter: a) dyrkning af PER.C6-celler i suspension i en bioreaktor med et perfusionssystem; b) inficering af cellerne i en bioreaktor ved en densitet på mellem 10 x 106 levedygtige celler/ml og 16 x 106 levedygtige celler/ml med rAd35; c) yderligere dyrkning af de inficerede celler i en bioreaktor med et perfusionssystem til opformering af rAd35; og d) høst af rAd35.
2. Fremgangsmåde ifølge krav 1, hvor cellerne in trin b) inficeres med rAd35 ved en densitet på mellem ca. 10 x 106 og 14 x 106 levedygtige celler/ml.
3. Fremgangsmåde ifølge et hvilket som helst af ovennævnte krav, hvor perfusionssystemet i trin c) er et perfusionssystem med alternerende tangentialt flow (ATF).
4. Fremgangsmåde ifølge et hvilket som helst af ovennævnte krav, der yderligere omfatter: e) oprensning af rAd35 og eventuelt f) fremstilling af et farmaceutisk præparat, der indeholder det oprensede rAd35.
5. Fremgangsmåde ifølge et hvilket som helst af ovennævnte krav, hvor det rekombinante adenovirus mangler mindst en del af El-området og omfatter heterolog nukleinsyre.
6. Fremgangsmåde ifølge et hvilket som helst af ovennævnte krav, hvor perfusionssystemet i trin a) er et perfusionssystem med alternerende tangentialt flow (ATF).
7. Fremgangsmåde ifølge et hvilket som helst af ovennævnte krav, hvor trin a) udføres i en første bioreaktor, og trin b) og c) udføres i en anden bioreaktor.
DK09744140.6T 2008-11-03 2009-10-29 Fremgangsmåde til produktion af adenovirusvektorer DK2350268T3 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US19812208P 2008-11-03 2008-11-03
EP08168181 2008-11-03
PCT/EP2009/064265 WO2010060719A1 (en) 2008-11-03 2009-10-29 Method for the production of adenoviral vectors

Publications (1)

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DK2350268T3 true DK2350268T3 (da) 2015-03-23

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DK09744140.6T DK2350268T3 (da) 2008-11-03 2009-10-29 Fremgangsmåde til produktion af adenovirusvektorer

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US (1) US10041049B2 (da)
EP (1) EP2350268B1 (da)
JP (1) JP5770633B2 (da)
KR (1) KR101504392B1 (da)
CN (1) CN102203242B (da)
AU (1) AU2009319254B2 (da)
BR (1) BRPI0921651A2 (da)
CA (1) CA2742474C (da)
DK (1) DK2350268T3 (da)
EA (1) EA019928B1 (da)
ES (1) ES2532015T3 (da)
HK (1) HK1160664A1 (da)
MX (1) MX2011004292A (da)
NZ (1) NZ593235A (da)
PL (1) PL2350268T3 (da)
WO (1) WO2010060719A1 (da)

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US20110207202A1 (en) 2011-08-25
MX2011004292A (es) 2011-05-31
AU2009319254B2 (en) 2015-04-30
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CN102203242A (zh) 2011-09-28
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