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 PDFInfo
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- 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
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Claims (14)
- EFFEKTIV AFGIVELSE AF STORE GENER VED HJÆLP AF DUAL-AAV-VEKTORER1. 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. 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. 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. 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. Dualkonstruktionssystem ifølge krav 4, hvor den kodende sekvens er valgt fra gruppen bestående af: ABCA4, MY07A, CEP290, CDH23, EYS, USH2a, GPR98 eller ALMS1.
- 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. 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. Værtscelle, der omfatter det virale dualvektorsystem ifølge et hvilket som helst af kravene 6 til 7.
- 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. 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. 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. 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. 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. 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.
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Families Citing this family (98)
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)
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 |
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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 |
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