[go: up one dir, main page]

DK2986635T3 - Effektiv afgivelse af store gener ved hjælp af dual-aav-vektorer - Google Patents

Effektiv afgivelse af store gener ved hjælp af dual-aav-vektorer Download PDF

Info

Publication number
DK2986635T3
DK2986635T3 DK14721802.8T DK14721802T DK2986635T3 DK 2986635 T3 DK2986635 T3 DK 2986635T3 DK 14721802 T DK14721802 T DK 14721802T DK 2986635 T3 DK2986635 T3 DK 2986635T3
Authority
DK
Denmark
Prior art keywords
aav
dual
vectors
sequence
plasmid
Prior art date
Application number
DK14721802.8T
Other languages
English (en)
Inventor
Alberto Auricchio
Pasqualina Colella
Ivana Trapani
Original Assignee
Fond Telethon
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Fond Telethon filed Critical Fond Telethon
Application granted granted Critical
Publication of DK2986635T3 publication Critical patent/DK2986635T3/da

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K48/00Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
    • A61K48/005Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
    • 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
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • C12N15/86Viral vectors
    • 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
    • C12N2750/00MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssDNA viruses
    • C12N2750/00011Details
    • C12N2750/14011Parvoviridae
    • C12N2750/14111Dependovirus, e.g. adenoassociated viruses
    • C12N2750/14141Use of virus, viral particle or viral elements as a vector
    • C12N2750/14143Use 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
    • C12N2800/00Nucleic acids vectors
    • C12N2800/40Systems of functionally co-operating vectors
    • 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
    • C12N2840/00Vectors comprising a special translation-regulating system
    • C12N2840/20Vectors comprising a special translation-regulating system translation of more than one cistron
    • 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
    • C12N2840/00Vectors comprising a special translation-regulating system
    • C12N2840/44Vectors comprising a special translation-regulating system being a specific part of the splice mechanism, e.g. donor, acceptor
    • 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
    • C12N2840/00Vectors comprising a special translation-regulating system
    • C12N2840/44Vectors comprising a special translation-regulating system being a specific part of the splice mechanism, e.g. donor, acceptor
    • C12N2840/445Vectors comprising a special translation-regulating system being a specific part of the splice mechanism, e.g. donor, acceptor for trans-splicing, e.g. polypyrimidine tract, branch point splicing

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Wood Science & Technology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Medicinal Chemistry (AREA)
  • Microbiology (AREA)
  • Plant Pathology (AREA)
  • Physics & Mathematics (AREA)
  • Virology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Toxicology (AREA)
  • Immunology (AREA)
  • Cell Biology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Claims (14)

  1. EFFEKTIV AFGIVELSE AF STORE GENER VED HJÆLP AF DUAL-AAV-VEKTORER
    1. Dualkonstruktionssystem til ekspression af den kodende sekvens for et gen af interesse i en værtscelle, idet den kodende sekvens består af en 5'-endedel og af en 3'-endedel, hvilket dualkonstruktionssystem omfatter: a) et første plasmid, der i en 5'-3'-retning omfatter: - en AAV 5'-inverteret terminal gentagelses-(5'-ITR)-sekvens; - en promotorsekvens; - 5'-endedelen af den kodende sekvens, idet 5'-endedelen er operabelt forbundet med og under styring af promotoren; - en nukleinsyresekvens for et splejsningsdonorsignal; og - en AAV 3'-inverteret terminal gentagelses-(3'-ITR)-sekvens; og b) et andet plasmid, der i en 5'-3'-retning omfatter: - en AAV 5'-inverteret terminal gentagelses-(5'-ITR)-sekvens; - en nukleinsyresekvens for et splejsningsacceptorsignal; - 3'-enden af den kodende sekvens; - en polyadenyleringssignalnukleinsyresekvens; og - en AAV 3'-inverteret terminal gentagelses-(3'-ITR)-sekvens, hvor det første plasmid endvidere omfatter en nukleinsyresekvens for en rekombinogen region i 5'-positionen i AAV 3'-ITR'en i det første plasmid og i 3'-positionen i nukleinsyresekvensen for splejsningsdonorsignalet, og hvor det andet plasmid endvidere omfatternukleinsyresekvensen forden rekombinogene region i 3'-positionen i AAV5'-ITR'en i det andet plasmid og i 5'-positionen i nukleinsyresekvensen forsplejsningsacceptorsignalet, hvor den rekombinogene region er en rekombinogen region i en F1-fag, der består af sekvensen: GGGATTTTGCCGATTTCGGCCTATTGGTTAAAAAATGAGCTGATTTAACAAAAATTTAA CGC GAATTTTAACAAAAT (SEQ ID No. 3) eller et fragment deraf, som bibeholder den rekombinogene egenskab for SEQ ID No. 3, hvor den kodende sekvens efter indføring af det første plasmid og det andet plasmid i værtscellen rekonstituerer ved hjælp af splejsningsdonor- og splejsningsacceptorsignalerne.
  2. 2. Dualkonstruktionssystem ifølge krav 1, hvor nukleotidsekvensen for ITR'erne stammer fra den samme AAV-serotype eller fra forskellige AAV-serotyper, fortrinsvis hvor 3'-ITR'en i det første plasmid og 5'-ITR'en i det andet plasmid er fra den samme AAV-serotype, fortrinsvis hvor henholdsvis 5'-ITR'en og 3'-ITR'en i det første plasmid og 5'-ITR'en og 3'-ITR'en i det andet plasmid er fra forskellige AAV-serotyper, fortrinsvis hvor 5'-ITR'en i det første plasmid og 3'-ITR'en i det andet plasmid er fra forskellige AAV-serotyper.
  3. 3. Dualkonstruktionssystem ifølge et hvilket som helst af de foregående krav, hvor nukleinsyresekvensen for splejsningsdonorsignalet består af sekvensen: GTAAGTATCAAGGTTACAAGACAGGTTTAAGGAGACCAATAGAAACTGGGCTTGTCGA GACA GAGAAGACTCTTGCGTTTCT (SEQ ID No. 1), og/eller hvor nukleinsyresekvensen for splejsningsacceptorsignalet består af sekvensen GATAGGCACCTATTGGTCTTACTGACATCCACTTTGCCTTTCTCTCCACAG (SEQ ID No. 2).
  4. 4. Dualkonstruktionssystem ifølge et hvilket som helst af de foregående krav, hvor den kodende sekvens er en nukleotidsekvens, der koder for et protein, som kan korrigere en nedarvet retinal degeneration.
  5. 5. Dualkonstruktionssystem ifølge krav 4, hvor den kodende sekvens er valgt fra gruppen bestående af: ABCA4, MY07A, CEP290, CDH23, EYS, USH2a, GPR98 eller ALMS1.
  6. 6. Viralt dual-adeno-associeret virus-(AAV)-vektorsystem, der omfatter: a) en første viral AAV-vektor, der indeholder det første plasmid som defineret i et hvilket som helst af kravene 1 til 5, og b) en anden viral AAV-vektor, der indeholder det andet plasmid som defineret i et hvilket som helst af kravene 1 til 5.
  7. 7. Viralt dual-AAV-vektorsystem ifølge krav 6, hvor adeno-associeret virus-(AAV)-vektorerne er valgt fra den samme eller forskellige AAV-serotyper, fortrinsvis hvor det adeno-associerede virus er valgt fra serotypen 2, serotypen 8, serotypen 5, serotypen 7 eller serotypen 9.
  8. 8. Værtscelle, der omfatter det virale dualvektorsystem ifølge et hvilket som helst af kravene 6 til 7.
  9. 9. Dualkonstruktionssystem ifølge et hvilket som helst af kravene 1 til 5, viralt dualvektorsystem ifølge et hvilket som helst af kravene 6 til 7 eller værtscelle ifølge krav 8 til medicinsk anvendelse, fortrinsvis til anvendelse ved genterapi.
  10. 10. Dualkonstruktionssystem, viralt dual vektorsystem, værtscelle ifølge krav 9 til anvendelse ved behandling og/eller forebyggelse af en patologi eller sygdom, der er kendetegnet ved en retinal degeneration, fortrinsvis hvor den retinale degeneration er nedarvet, fortrinsvis hvor patologien eller sygdommen er valgt fra gruppen bestående af: retinitis pigmentosa, Lebers kongenitale amaurose (LCA), Stargardt-sygdom, Usher-sygdom, Alstrom-syndrom, en sygdom forårsaget af en mutation i ABCA4-ger\et.
  11. 11. Farmaceutisk sammensætning, der omfatter dualkonstruktionssystemet ifølge et hvilket som helst af kravene 1 til 5, det virale dualvektorsystem ifølge et hvilket som helst af kravene 6 til 7 eller værtscellen ifølge krav 8 og et farmaceutisk acceptabelt vehikel.
  12. 12. Nukleinsyre bestående af SEQ ID No. 3 eller et fragment deraf, som bibeholder den rekombinogene egenskab for SEQ ID No. 3, til anvendelse som en rekombinogen region.
  13. 13. In v/'fro-fremgangsmåde til induktion af genetisk rekombination, hvilken fremgangsmåde omfatter anvendelse af sekvensen bestående af SEQ ID No. 3 eller et fragment deraf, som bibeholder den rekombinogene egenskab for SEQ ID No. 3.
  14. 14. Sekvens bestående af SEQ ID No. 3 eller et fragment deraf, som bibeholder den rekombinogene egenskab for SEQ ID No. 3, til anvendelse ved en behandlingsfremgangsmåde, fortrinsvis ved hjælp af genterapi, hvor fremgangsmåden inducerer genetisk rekombination.
DK14721802.8T 2013-04-18 2014-04-18 Effektiv afgivelse af store gener ved hjælp af dual-aav-vektorer DK2986635T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361813342P 2013-04-18 2013-04-18
PCT/EP2014/058000 WO2014170480A1 (en) 2013-04-18 2014-04-18 Effective delivery of large genes by dual aav vectors

Publications (1)

Publication Number Publication Date
DK2986635T3 true DK2986635T3 (da) 2019-01-28

Family

ID=50678160

Family Applications (1)

Application Number Title Priority Date Filing Date
DK14721802.8T DK2986635T3 (da) 2013-04-18 2014-04-18 Effektiv afgivelse af store gener ved hjælp af dual-aav-vektorer

Country Status (11)

Country Link
US (2) USRE50283E1 (da)
EP (1) EP2986635B1 (da)
JP (1) JP6453307B2 (da)
CN (1) CN105408352B (da)
AU (1) AU2014255665B2 (da)
CA (1) CA2909733C (da)
DK (1) DK2986635T3 (da)
EA (1) EA034575B1 (da)
ES (1) ES2704677T3 (da)
MX (1) MX365711B (da)
WO (1) WO2014170480A1 (da)

Families Citing this family (98)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9217155B2 (en) 2008-05-28 2015-12-22 University Of Massachusetts Isolation of novel AAV'S and uses thereof
US8734809B2 (en) 2009-05-28 2014-05-27 University Of Massachusetts AAV's and uses thereof
CA3050894C (en) 2010-04-23 2022-10-18 University Of Massachusetts Multicistronic expression constructs
CA2833908C (en) 2010-04-23 2021-02-09 University Of Massachusetts Cns targeting aav vectors and methods of use thereof
WO2013075008A1 (en) 2011-11-16 2013-05-23 University Of Florida Research Foundation Inc. Aav dual vector systems for gene therapy
EA034575B1 (ru) 2013-04-18 2020-02-21 Фондацьоне Телетон Эффективная доставка больших генов посредством двойных aav векторов
WO2015127128A2 (en) 2014-02-19 2015-08-27 University Of Massachusetts Recombinant aavs having useful transcytosis properties
ES2856403T3 (es) 2014-03-18 2021-09-27 Univ Massachusetts Composiciones a base de rAAV y procedimientos para el tratamiento de la esclerosis lateral amiotrofica
US10689653B2 (en) 2014-06-03 2020-06-23 University Of Massachusetts Compositions and methods for modulating dysferlin expression
WO2015191508A1 (en) 2014-06-09 2015-12-17 Voyager Therapeutics, Inc. Chimeric capsids
WO2016054554A1 (en) 2014-10-03 2016-04-07 University Of Massachusetts Heterologous targeting peptide grafted aavs
WO2016065001A1 (en) 2014-10-21 2016-04-28 University Of Massachusetts Recombinant aav variants and uses thereof
JP6401871B2 (ja) 2014-11-05 2018-10-10 ボイジャー セラピューティクス インコーポレイテッドVoyager Therapeutics,Inc. パーキンソン病の治療のためのaadcポリヌクレオチド
HK1244299A1 (zh) 2014-11-14 2018-08-03 Voyager Therapeutics, Inc. 治療肌萎縮側索硬化(als)的組合物和方法
SG11201703419UA (en) 2014-11-14 2017-05-30 Voyager Therapeutics Inc Modulatory polynucleotides
US10584321B2 (en) 2015-02-13 2020-03-10 University Of Massachusetts Compositions and methods for transient delivery of nucleases
HRP20220776T1 (hr) * 2015-03-03 2022-09-16 Fondazione Telethon Sustav višestrukih vektora i njegova upotreba
WO2016172008A1 (en) 2015-04-24 2016-10-27 University Of Massachusetts Modified aav constructions and uses thereof
WO2016193434A1 (en) 2015-06-04 2016-12-08 INSERM (Institut National de la Santé et de la Recherche Médicale) Improved methods for treating ocular diseases by gene therapy
WO2017070525A1 (en) 2015-10-22 2017-04-27 University Of Massachusetts Methods and compositions for treating metabolic imbalance in neurodegenerative disease
EP3364996B1 (en) 2015-10-22 2021-08-25 University of Massachusetts Prostate-targeting adeno-associated virus serotype vectors
AU2016355343C1 (en) 2015-11-19 2024-10-03 Lloyd G. Mitchell Compositions and methods for correction of heritable ocular disease
US11090392B2 (en) * 2015-12-14 2021-08-17 The Trustees Of The University Of Pennsylvania Gene therapy for ocular disorders
EP3393522B1 (en) * 2015-12-22 2021-07-07 INSERM (Institut National de la Santé et de la Recherche Médicale) Improved hybrid dual recombinant aav vector systems for gene therapy
US11826433B2 (en) 2016-02-02 2023-11-28 University Of Massachusetts Method to enhance the efficiency of systemic AAV gene delivery to the central nervous system
US11060088B2 (en) 2016-02-12 2021-07-13 University Of Massachusetts Anti-angiogenic miRNA therapeutics for inhibiting corneal neovascularization
WO2017176929A1 (en) 2016-04-05 2017-10-12 University Of Massachusetts Compositions and methods for selective inhibition of grainyhead-like protein expression
WO2017181105A1 (en) 2016-04-15 2017-10-19 University Of Massachusetts Methods and compositions for treating metabolic imbalance
EP3448987A4 (en) 2016-04-29 2020-05-27 Voyager Therapeutics, Inc. COMPOSITIONS FOR THE TREATMENT OF DISEASES
KR102427379B1 (ko) 2016-05-18 2022-08-02 보이저 테라퓨틱스, 인크. 헌팅톤 질환을 치료하기 위한 조성물 및 방법
JP7066635B2 (ja) 2016-05-18 2022-05-13 ボイジャー セラピューティクス インコーポレイテッド 調節性ポリヌクレオチド
WO2017218852A1 (en) 2016-06-15 2017-12-21 University Of Massachusetts Recombinant adeno-associated viruses for delivering gene editing molecules to embryonic cells
JP2019523648A (ja) * 2016-06-15 2019-08-29 オックスフォード ユニバーシティ イノベーション リミテッドOxford University Innovation Limited Abc4aを発現させるためのデュアル重複アデノ随伴ウイルスベクターシステム
US20190185864A1 (en) * 2016-08-23 2019-06-20 Akouos, Inc. Compositions and methods for treating non-age-associated hearing impairment in a human subject
JP2019531787A (ja) 2016-08-30 2019-11-07 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア 生物医学的ターゲティング及びデリバリーの方法並びにそれを実行するための装置及びシステム
US10457940B2 (en) 2016-09-22 2019-10-29 University Of Massachusetts AAV treatment of Huntington's disease
KR20190075964A (ko) 2016-10-13 2019-07-01 유니버시티 오브 매사추세츠 Aav 캡시드 설계
CN110914419A (zh) * 2017-03-10 2020-03-24 吉尼松公司 糖原贮积病iii的治疗
JP7307480B2 (ja) * 2017-04-05 2023-07-12 ユニバーシティ オブ マサチューセッツ ミニ遺伝子療法
US11773409B2 (en) 2017-04-21 2023-10-03 The Board Of Trustees Of The Leland Stanford Junior University CRISPR/Cas 9-mediated integration of polynucleotides by sequential homologous recombination of AAV donor vectors
EP3618839A4 (en) 2017-05-05 2021-06-09 Voyager Therapeutics, Inc. Compositions and methods of treating amyotrophic lateral sclerosis (als)
SG11201909868YA (en) 2017-05-05 2019-11-28 Voyager Therapeutics Inc Compositions and methods of treating huntington's disease
AU2018261769B2 (en) * 2017-05-05 2024-03-14 The Regents Of The University Of California Compositions and methods for expressing Otoferlin
WO2018208972A1 (en) 2017-05-09 2018-11-15 University Of Massachusetts Methods of treating amyotrophic lateral sclerosis (als)
JP2020527335A (ja) 2017-06-14 2020-09-10 ザ・トラステイーズ・オブ・ザ・ユニバーシテイ・オブ・ペンシルベニア 眼疾患のための遺伝子療法
JOP20190269A1 (ar) 2017-06-15 2019-11-20 Voyager Therapeutics Inc بولي نوكليوتيدات aadc لعلاج مرض باركنسون
CN111132626B (zh) 2017-07-17 2024-01-30 沃雅戈治疗公司 轨迹阵列引导系统
EP3808849A1 (en) 2017-08-03 2021-04-21 Voyager Therapeutics, Inc. Compositions and methods for delivery of aav
JP7397488B2 (ja) 2017-09-22 2023-12-13 ユニバーシティ オブ マサチューセッツ Sod1二重発現ベクターおよびその使用
MX2020003042A (es) 2017-09-29 2020-11-18 Voyager Therapeutics Inc Rescate del fenotipo neurológico central y periférico de la ataxia de friedreich mediante administración intravenosa.
KR102735096B1 (ko) * 2017-10-11 2024-11-28 (주)셀트리온 고발현 및 고기능성 목적 단백질의 생산을 위한 발현 카세트 및 이의 이용
US20200237799A1 (en) 2017-10-16 2020-07-30 Voyager Therapeutics, Inc. Treatment of amyotrophic lateral sclerosis (als)
US11434502B2 (en) 2017-10-16 2022-09-06 Voyager Therapeutics, Inc. Treatment of amyotrophic lateral sclerosis (ALS)
WO2019118516A1 (en) * 2017-12-11 2019-06-20 Editas Medicine, Inc. Cpf1-related methods and compositions for gene editing
MA51918A (fr) * 2018-02-22 2020-12-30 Akouos Inc Compositions et méthodes de traitement d'une hypoacousie non associée à l'âge chez un sujet humain
US20210147870A1 (en) 2018-04-05 2021-05-20 Nightstarx Limited Compositions and methods for the treatment of stargardt disease
CA3097004A1 (en) * 2018-04-17 2019-10-24 The Trustees Of The University Of Pennsylvania Trans-splicing molecules
US11660353B2 (en) * 2018-04-27 2023-05-30 Decibel Therapeutics, Inc. Compositions and methods for treating sensorineural hearing loss using otoferlin dual vector systems
US12233136B2 (en) 2018-04-27 2025-02-25 Decibel Therapeutics, Inc. Myosin 15 promoters and uses thereof
AU2019268330A1 (en) 2018-05-15 2020-11-26 Voyager Therapeutics, Inc. Compositions and methods for the treatment of Parkinson's disease
EP3802829A4 (en) 2018-06-08 2022-10-19 University of Massachusetts ANTISENSE OLIGONUCLEOTIDES TO RESTORE DYSFERLIN PROTEIN EXPRESSION IN CELLS FROM PATIENTS WITH DYSFERLINOPATHY
BR112020026606A2 (pt) * 2018-06-25 2021-04-06 Akouos, Inc. Métodos de tratamento de perda auditiva e/ou perda de visão associada à clrn1
EP3821019A4 (en) * 2018-07-13 2022-10-05 Akouos, Inc. METHODS OF TREATMENT OF NONSYNDROMIC INNER EAR DEAF
CN109136266B (zh) * 2018-08-10 2022-02-18 深圳泓熙生物科技发展有限公司 用于治疗或预防结晶样视网膜色素变性的基因载体及其用途
SG11202103151RA (en) 2018-09-28 2021-04-29 Voyager Therapeutics Inc Frataxin expression constructs having engineered promoters and methods of use thereof
CN113365603B (zh) * 2018-10-11 2025-04-11 分贝治疗公司 Aav1载体及其用于治疗耳部适应症的用途
WO2020079034A2 (en) 2018-10-15 2020-04-23 Fondazione Telethon Intein proteins and uses thereof
US12188041B2 (en) * 2018-11-01 2025-01-07 University Of Florida Research Foundation, Incorporated Codon optimized otoferlin AAV dual vector gene therapy
CA3119059A1 (en) * 2018-11-07 2020-05-14 Akouos, Inc. Compositions and methods of inducing differentiation of a hair cell
US20230056182A1 (en) * 2018-11-07 2023-02-23 Akouos, Inc. Use of adeno-associated viral vectors to correct gene defects/ express proteins in hair cells and supporting cells in the inner ear
SG11202106356QA (en) * 2018-12-20 2021-07-29 Vigeneron Gmbh An optimized acceptor splice site module for biological and biotechnological applications
AU2020218547A1 (en) 2019-02-08 2021-08-26 Decibel Therapeutics, Inc. Myosin 15 promoters and uses thereof
AU2020260154A1 (en) * 2019-04-17 2021-11-11 The Trustees Of The University Of Pennsylvania Triple helix terminator for efficient RNA trans-splicing
WO2020214990A1 (en) * 2019-04-17 2020-10-22 Ascidian Therapeutics, Inc. Abca4 cell line and methods of use
US20220202959A1 (en) * 2019-04-19 2022-06-30 University Of Massachusetts Gene therapies for usher syndrome (ush2a)
WO2020214797A1 (en) * 2019-04-19 2020-10-22 University Of Massachusetts Gene therapies for usher syndrome (ush1b)
WO2020236815A1 (en) * 2019-05-20 2020-11-26 University Of Massachusetts Minigene therapy
US20220348953A1 (en) * 2019-06-25 2022-11-03 Migal Galilee Research Institute Ltd. SYSTEMS AND USES THEREOF FOR CREATING SYNTHETIC TRANSCRIPTIONAL LOGIC 'AND' GATES BASED ON PRE-mRNA TRANS-SPLICING
US20220267802A1 (en) * 2019-07-15 2022-08-25 President And Fellows Of Harvard College Methods and compositions for gene delivery
JP7665609B2 (ja) * 2019-10-30 2025-04-21 デシベル セラピューティクス インコーポレイテッド オトフェリン二重ベクター系及びそれを含む感音難聴を治療するための組成物
EP4073257A1 (en) * 2019-12-09 2022-10-19 UCL Business Ltd Gene therapy composition and treatment for myh7-linked cardiomyopathy
CN113122657B (zh) * 2019-12-31 2022-07-29 上海吉凯基因医学科技股份有限公司 一种多重aav病毒滴度的检测方法
CA3168055A1 (en) 2020-02-21 2021-08-26 Emmanuel John Simons Compositions and methods for treating non-age-associated hearing impairment in a human subject
WO2021202817A1 (en) * 2020-04-01 2021-10-07 University Of Florida Research Foundation, Incorporated Dual aav-myo7a vectors with improved safety for the treatment of ush1b
IL297718A (en) * 2020-04-29 2022-12-01 Saliogen Therapeutics Inc Preparations and methods for the treatment of hereditary macular degeneration
CA3184489A1 (en) * 2020-07-14 2022-01-20 Abeona Therapeutics Inc. Recombinant adeno-associated viral vectors for multipartite gene delivery
CN111926085B (zh) * 2020-08-21 2022-05-31 云南农业大学 一种影响鸡肌肉亮度的分子标记及其应用
IL303269A (en) 2020-12-03 2023-07-01 Century Therapeutics Inc Genetically engineered cells and uses thereof
US11661459B2 (en) 2020-12-03 2023-05-30 Century Therapeutics, Inc. Artificial cell death polypeptide for chimeric antigen receptor and uses thereof
AU2021401052A1 (en) 2020-12-18 2023-06-22 Century Therapeutics, Inc. Chimeric antigen receptor systems with adaptable receptor specificity
US20240102048A1 (en) * 2021-02-12 2024-03-28 Greffex, Inc. Gene therapy for retinal diseases
US11603541B2 (en) 2021-05-06 2023-03-14 Kinase Pharma Inc. Compositions and method of making a complex able to increase production of a cetuximab-like protein (CLP) in a target cell
US20220389450A1 (en) * 2021-05-12 2022-12-08 Fondazione Telethon Vector system
CN115074369B (zh) * 2022-06-24 2023-10-20 成都金唯科生物科技有限公司 表达全长abca4基因的腺相关病毒载体及应用
CN118345117A (zh) * 2023-01-16 2024-07-16 苏州吉恒基因科技有限公司 重组腺相关病毒大基因包装表达载体的构建生产和用途
WO2024229049A1 (en) * 2023-05-01 2024-11-07 University Of Florida Research Foundation, Incorporated Dual aav vectors for treating stargardt disease
US20240376494A1 (en) * 2023-05-08 2024-11-14 Wisconsin Alumni Research Foundation Recombinant aav constructs for increased transgene expression
WO2025029171A1 (ru) * 2023-07-29 2025-02-06 Общество с ограниченной ответственностью "Генетические технологии" (ООО "Генетические технологии") Векторы экспрессии на основе аденоассоциированного вируса

Family Cites Families (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5166331A (en) 1983-10-10 1992-11-24 Fidia, S.P.A. Hyaluronics acid fractions, methods for the preparation thereof, and pharmaceutical compositions containing same
EP0356130A3 (en) 1988-08-22 1991-09-11 Genencor International, Inc. A mobile fl phage single-strand dna origin of replication
US6255071B1 (en) * 1996-09-20 2001-07-03 Cold Spring Harbor Laboratory Mammalian viral vectors and their uses
FR2763959A1 (fr) 1997-06-02 1998-12-04 Transgene Sa Nouveaux vecteurs adenoviraux recombinants comprenant une sequence d'epissage
GB9720465D0 (en) 1997-09-25 1997-11-26 Oxford Biomedica Ltd Dual-virus vectors
GB9803351D0 (en) 1998-02-17 1998-04-15 Oxford Biomedica Ltd Anti-viral vectors
US6846970B1 (en) * 1999-07-19 2005-01-25 Plant Bioscience Limited Transformation method and transgenic plants produced thereby
US6544786B1 (en) 1999-10-15 2003-04-08 University Of Pittsburgh Of The Commonwealth Of Higher Education Method and vector for producing and transferring trans-spliced peptides
GB0009760D0 (en) 2000-04-19 2000-06-07 Oxford Biomedica Ltd Method
EP1496980A4 (en) 2002-04-19 2005-06-22 Georgia Tech Res Inst COMPOSITIONS AND METHODS FOR ACCELERATING PROTEIN SECRETION DYNAMICS
JP4528623B2 (ja) 2002-09-16 2010-08-18 プロメガ コーポレイション 迅速分解性レポーター融合タンパク質
US20050101582A1 (en) 2003-11-12 2005-05-12 Allergan, Inc. Compositions and methods for treating a posterior segment of an eye
US20120283232A9 (en) 2003-11-12 2012-11-08 Zhengjun Wang Process for making a pharmaceutical composition
US20070224278A1 (en) 2003-11-12 2007-09-27 Lyons Robert T Low immunogenicity corticosteroid compositions
US20060141049A1 (en) 2003-11-12 2006-06-29 Allergan, Inc. Triamcinolone compositions for intravitreal administration to treat ocular conditions
AU2005209201B2 (en) 2004-01-20 2010-06-03 Allergan, Inc. Compositions for localized therapy of the eye, comprising preferably triamcinolone acetonide and hyaluronic acid
US20050244472A1 (en) 2004-04-30 2005-11-03 Allergan, Inc. Intraocular drug delivery systems containing excipients with reduced toxicity and related methods
US20070059336A1 (en) 2004-04-30 2007-03-15 Allergan, Inc. Anti-angiogenic sustained release intraocular implants and related methods
US20060182783A1 (en) 2004-04-30 2006-08-17 Allergan, Inc. Sustained release intraocular drug delivery systems
WO2006043965A1 (en) 2004-10-14 2006-04-27 Allergan, Inc. Therapeutic ophthalmic compositions containing retinal friendly excipients and related methods
US7410765B2 (en) 2004-11-17 2008-08-12 The Regents Of The University Of California System for protease mediated protein expression
US20090082321A1 (en) 2007-09-21 2009-03-26 Allergan, Inc. Steroid containing drug delivery systems
JP4948845B2 (ja) 2006-02-08 2012-06-06 財団法人 東京都医学総合研究所 神経変性疾患治療用物質のスクリーニング方法
US8470965B2 (en) * 2006-03-01 2013-06-25 University Of Utah Research Foundation Methods and compositions related to cyclic peptide synthesis
CA2644952A1 (en) 2006-03-01 2007-09-13 The University Of Utah Research Foundation Methods and compositions related to cyclic peptide synthesis
JP5332064B2 (ja) * 2007-03-01 2013-11-06 ウェルスタット イムノセラピューティクス, エルエルシー 炎症により特徴付けられる疾患の治療
US8642067B2 (en) 2007-04-02 2014-02-04 Allergen, Inc. Methods and compositions for intraocular administration to treat ocular conditions
US20090214478A1 (en) * 2008-02-21 2009-08-27 Alberto Auricchio Method of treating ocular diseases by gene therapy
WO2009132455A1 (en) 2008-04-30 2009-11-05 Paul Xiang-Qin Liu Protein splicing using short terminal split inteins
US8236557B2 (en) * 2008-05-28 2012-08-07 University Of Missouri-Columbia Hybrid-AAV vectors to deliver large gene expression cassette
US20100098772A1 (en) 2008-10-21 2010-04-22 Allergan, Inc. Drug delivery systems and methods for treating neovascularization
CA2744153C (en) 2008-11-19 2020-07-07 Amyris, Inc. Compositions and methods for the assembly of polynucleotides
MX352265B (es) 2009-07-02 2017-11-16 Merz Pharma Gmbh & Co Kgaa Neurotoxinas que exhiben actividad biologica acortada.
DK2761006T3 (da) 2011-09-28 2017-03-27 Zera Intein Protein Solutions S L Spaltede inteiner og anvendelser deraf
WO2013075008A1 (en) * 2011-11-16 2013-05-23 University Of Florida Research Foundation Inc. Aav dual vector systems for gene therapy
EA034575B1 (ru) 2013-04-18 2020-02-21 Фондацьоне Телетон Эффективная доставка больших генов посредством двойных aav векторов
NZ758021A (en) 2013-10-11 2021-12-24 Massachusetts Eye & Ear Infirmary Methods of predicting ancestral virus sequences and uses thereof
GB201403684D0 (en) 2014-03-03 2014-04-16 King S College London Vector
HRP20220776T1 (hr) 2015-03-03 2022-09-16 Fondazione Telethon Sustav višestrukih vektora i njegova upotreba
US11007280B2 (en) 2015-03-17 2021-05-18 Vrije Universiteit Brussel Optimized liver-specific expression systems for FVIII and FIX
CN108603235A (zh) 2015-07-30 2018-09-28 马萨诸塞眼科耳科诊所 祖先病毒序列及其用途
US11142550B2 (en) 2016-01-29 2021-10-12 The Trustees Of Princeton University Split inteins with exceptional splicing activity
JP2019523648A (ja) 2016-06-15 2019-08-29 オックスフォード ユニバーシティ イノベーション リミテッドOxford University Innovation Limited Abc4aを発現させるためのデュアル重複アデノ随伴ウイルスベクターシステム
AU2017342543B2 (en) 2016-10-14 2024-06-27 President And Fellows Of Harvard College AAV delivery of nucleobase editors
AU2018227440B2 (en) 2017-02-28 2024-06-06 The Trustees Of The University Of Pennsylvania Adeno-associated virus (AAV) clade f vector and uses therefor
WO2020079034A2 (en) 2018-10-15 2020-04-23 Fondazione Telethon Intein proteins and uses thereof
US20220389450A1 (en) 2021-05-12 2022-12-08 Fondazione Telethon Vector system

Also Published As

Publication number Publication date
MX365711B (es) 2019-06-11
EP2986635A1 (en) 2016-02-24
MX2015014423A (es) 2016-07-28
US10494645B2 (en) 2019-12-03
AU2014255665A1 (en) 2015-11-12
US20160076054A1 (en) 2016-03-17
JP2016516424A (ja) 2016-06-09
USRE50283E1 (en) 2025-01-28
WO2014170480A1 (en) 2014-10-23
ES2704677T3 (es) 2019-03-19
CA2909733C (en) 2023-10-17
CN105408352A (zh) 2016-03-16
CA2909733A1 (en) 2014-10-23
EA034575B1 (ru) 2020-02-21
EP2986635B1 (en) 2018-10-03
BR112015026422A2 (pt) 2017-11-14
AU2014255665B2 (en) 2018-08-02
JP6453307B2 (ja) 2019-01-16
CN105408352B (zh) 2020-01-14
EA201591992A1 (ru) 2016-04-29

Similar Documents

Publication Publication Date Title
DK2986635T3 (da) Effektiv afgivelse af store gener ved hjælp af dual-aav-vektorer
KR102240180B1 (ko) 다중 벡터 시스템 및 이의 용도
KR20200051011A (ko) 변형된 폐쇄-종결된 dna(cedna)
AU2025200031A1 (en) Cellular models of and therapies for ocular diseases
KR20200057766A (ko) 페닐케톤뇨증을 치료하기 위한 프로모터 및 인핸서 조합을 포함하는 벡터
KR20200107949A (ko) 조작된 dna 결합 단백질
KR20190136048A (ko) 페닐케톤뇨증을 치료하기 위한 조성물 및 방법
CN116194154A (zh) 使用aav载体的plakophilin-2(pkp2)基因疗法
KR20210119416A (ko) 폐쇄-말단 dna (cedna), 및 유전자 또는 핵산 치료 관련 면역 반응을 감소시키는 방법에서의 이의 용도
CN114126665B (zh) 眼底黄色斑点症(abca4)的基因疗法
CN116685329B (zh) 核酸构建体及其用于治疗脊髓性肌肉萎缩症的用途
KR20220140537A (ko) Cdkl5 결핍 장애를 치료하기 위한 유전자 요법
RU2761879C1 (ru) Вакцина на основе AAV5 для индукции специфического иммунитета к вирусу SARS-CoV-2 и/или профилактики коронавирусной инфекции, вызванной SARS-CoV-2
KR20230042468A (ko) Csrp3 (시스테인 및 글리신 풍부 단백질 3) 유전자 요법
CN112639107B (zh) 治疗clrn1相关的听力损失和/或视力损失的方法
KR20240005950A (ko) 벡터 시스템
TW202229321A (zh) 核酸構築體、病毒載體及病毒顆粒
CN115244181A (zh) 阿司匹林化合物在增加核酸表达中的新型用途
RU2800026C2 (ru) МОДИФИЦИРОВАННАЯ ДНК С ЗАМКНУТЫМИ КОНЦАМИ (зкДНК)
RU2816963C2 (ru) МОДИФИЦИРОВАННАЯ ДНК С ЗАМКНУТЫМИ КОНЦАМИ (зкДНК), СОДЕРЖАЩАЯ СИММЕТРИЧНЫЕ МОДИФИЦИРОВАННЫЕ ИНВЕРТИРОВАННЫЕ КОНЦЕВЫЕ ПОВТОРЫ
RU2829367C2 (ru) ДНК С ЗАМКНУТЫМИ КОНЦАМИ (зкДНК) И ПРИМЕНЕНИЕ В СПОСОБАХ УМЕНЬШЕНИЯ ИММУННОГО ОТВЕТА, СВЯЗАННОГО С ГЕННОЙ ТЕРАПИЕЙ ИЛИ ТЕРАПИЕЙ НУКЛЕИНОВОЙ КИСЛОТОЙ
RU2817770C2 (ru) Интеграция конструкций нуклеиновой кислоты в эукариотические клетки с транспозазой из oryzias
CN117836420A (zh) 重组tert编码病毒基因组和运载体
EA047326B1 (ru) СИНЕРГЕТИЧЕСКОЕ ДЕЙСТВИЕ SMN1 И miR-23a ПРИ ЛЕЧЕНИИ СПИНАЛЬНОЙ МЫШЕЧНОЙ АТРОФИИ
BR112015026422B1 (pt) Sistema de construto duplo para expressar a sequência de codificação de um gene de interesse em uma célula hospedeira, sistema de vetor viral vírus adenoassociado (aav) duplo, célula hospedeira microbiana, composição farmacêutica e método in vitro para induzir a recombinação genética