HUE029564T2 - Herpes simplex vírus vakcinák - Google Patents
Herpes simplex vírus vakcinák Download PDFInfo
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- HUE029564T2 HUE029564T2 HUE10840033A HUE10840033A HUE029564T2 HU E029564 T2 HUE029564 T2 HU E029564T2 HU E10840033 A HUE10840033 A HU E10840033A HU E10840033 A HUE10840033 A HU E10840033A HU E029564 T2 HUE029564 T2 HU E029564T2
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- A61K39/245—Herpetoviridae, e.g. herpes simplex virus
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- C12N2710/16011—Herpesviridae
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- C12N2710/00011—Details
- C12N2710/16011—Herpesviridae
- C12N2710/16611—Simplexvirus, e.g. human herpesvirus 1, 2
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- C12N2710/00011—Details
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- C12N2710/00011—Details
- C12N2710/16011—Herpesviridae
- C12N2710/16611—Simplexvirus, e.g. human herpesvirus 1, 2
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- C12N2830/002—Vector systems having a special element relevant for transcription controllable enhancer/promoter combination inducible enhancer/promoter combination, e.g. hypoxia, iron, transcription factor
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- C12N2830/005—Vector systems having a special element relevant for transcription controllable enhancer/promoter combination repressible enhancer/promoter combination, e.g. KRAB
- C12N2830/006—Vector systems having a special element relevant for transcription controllable enhancer/promoter combination repressible enhancer/promoter combination, e.g. KRAB tet repressible
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Claims (4)
- Herpes simplex vírus vakcinák SZABADALMI IGÉNYPONTOK.1, Replikáeii'-defektiv. dommáns-negatlv Herpes simplex vims 2: (IÏSV-2) rekombiráns virus, amely a genomjâban a következőket tartalmazza: a) : egy első szekvencia, amely egy első BSY-2 glíkoprotek D~t ígD2) kódol, ahol a szóban forgó szekvencia mikddés szempontjából egy első tei-ö-tartalmn HSY-1 €P4 promoterhez van kapcsolva; b) egy második szekvencia, amely egy második BSV-2 gD2-t kódol:, ahol a szóban forgó második szekvencia mnbödés szempontjából egy második tei-GAartalmú HSV-1 €P4 pvmm-terhez, van kapcsolva* e) egy harmadik szekvencia, amely egy első ül,9 C33SC felsőjét (2. számé szekvencia) kódol, ahol a szóba® lorgó harmadik szekvencia működés szempontjából egy első iet-Ö-lartalmú feCMV közvetlen közeli prornotérhez kapcsolódik, a teljes hosszúságú: promoter -236 bázis-párjánál egy csonkítással; és á) egy negyedik szekvencia, amely egy második 111,9 CS35C lobért# (2. számó szekvencia) kódol, aboi a szóban íorgő negyedik szekvencia működés szempontjából egy második lei-Ö-lartainiű hCMV közvetlen közel promoterhez kapcsolódik», a teljes hosszúságú promoter -236 bázispártjánál egy csonkítással; is ahol a szóban lorgó genom nem tartalmaz funkcionális iCPO iebéfjét. kódoló szekvenciái 2v Az I. igénypont .szerinti rekornbináns vírus, ahol: a) a. szóban forgó első és második tet-O-tartalmn 1ISY-1 CP4 promoterek, és a szóban íórgő első és második tet-Ö-íanalmú hCMV közvetlen közeli promoterek egyaránt rendelkeznek egy TATA elemmel; b) mindegyik szóban, forgó let A3-tartalmú promofer-szekveneia tartalmaz két op2 repressxor-: koto helyet, amelyeket 2-20 összekötő mádeotid kapcsol össze, ahol a szóban forgó tét operátorban m első ntáleotid a. 6. és 24. imkleotid közön található, a szóban forgó TATA elem utolsó nukleoiidjáíól 3' irányban; c) a szóban forgó első szekvencia, «amely egy HSV-2 gD2~l kódol., és a szóban forgó második szekvencia, amely egy HSV-2 gD2~t kódok a szóban forgó első és második Tet-O-tartalmá HSV-i CF4 promoterekhez viszonyítva 3 ’ irányban: helyezkedik el; d| a szóban forgó harmadik szekvencia, amely egy UL9 C535C fehérjéi (2. számú szekvencia) kódok és a szóban forgo 4, szekvencia, amely egy IJL9 CS35C ledénél (2. számú szekvencia) kódok a szóban forgó tet-Ö-tarlaimá i€MV közvetlen közeli pomoterekhez viszonyítva 3' irányban helyezkedik el...
- 3. Az 1. vagy 2. igénypont szerinti rekömbiafe 'vírus,, amely egy vagy több rekonfoinfeis Immun® odolále gént is enpresszáL példán! ILI 2-t vagy IL-IS-ot HSY-2 gB-í a letö-hordozó BSV vagy h€MY közvetlen-közeli promoter vezérlése alatt; és/vagy HSV-2 gC-t a tetO-lmrdozó BSV vagy hCMV közvetlen-közeli promoter vezérlése alatt 4:. Az 1. vagy 2. igénypont bármelyike szerinti rekomblnáps viras, amely a HSV-2 gB-i a tető-hordozó BSV vagy k€MV közvetlen-közeli promoter vezérlése alatt ezptesszáija.
- 5. Az 14. igénypontok bármelyike szerinti rekombináns vírus ahol a szóban lorgo harmadik, az UL9 €535C fehérjéi (2. szántó szekvencia) kódoló szekvencia transzkrípciqja. és a szóban forgó első. a HSV-2 gD2-t kódoló szekveneia. transzkripebija ellentétes orientációjú, és ahol a szóban .forgó negyedik, az ÜL9 C535C fehérjét (2, számú szekvencia) kódoló szekvencia transzkripciója és a sfobmvforgó második, a H SV-2 gD2-t kódoló szekveneia transzkripciója ellentétes orientációjú. 6. .½ 1-4, igénypontok bármelyike szerinti rekombináns vires, ahol az ICF4 ptonroierek-bői hiányzik egy 1CP4 DNS-kötő szekveneia.
- 7. Vakcina, amel}· az l-δ. igénypontok bármelyike szerinti rekombináns vírust tartalmazza, egységdózis formájába® 8. A 7, igénypont szerintii vakcina, amelyben a rekombináns vírus minimum IvlCk tarfbltképzo egység per egységdözis mennyiségben van jelen, példád 1 *.10"' - 1 ^ 1.0* per egységdózis mennyiségben, 9. A ?.. vagy 8, igénypont szerinti vakcina, egy beteg BSV-I vagy HSV-2 fertőzés elleni tmni nnízálásábaxí történő aik aim ázást® 10. A 7. vagy S. igénypont szerinti vakcina 9. igénypont szerinti alkalmazása, aboi a beteg: szeropozhiv a HSV-1, szeropozitiv a HSV-2, szcrogoziiív mind a HSV-L mind a HSV-2 fertőzésre, \agy szeronegativ a HSY-1 és HSV-2 fertőzésre.
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Application Number | Priority Date | Filing Date | Title |
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US28883609P | 2009-12-21 | 2009-12-21 |
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HUE029564T2 true HUE029564T2 (hu) | 2017-03-28 |
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HUE10840033A HUE029564T2 (hu) | 2009-12-21 | 2010-12-20 | Herpes simplex vírus vakcinák |
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US (3) | US8809047B2 (hu) |
EP (1) | EP2516629B1 (hu) |
JP (2) | JP5845191B2 (hu) |
KR (1) | KR101747987B1 (hu) |
CN (1) | CN102666843B (hu) |
AU (1) | AU2010333749B2 (hu) |
BR (1) | BR112012015172A2 (hu) |
CA (1) | CA2783330A1 (hu) |
DK (1) | DK2516629T3 (hu) |
HK (1) | HK1175807A1 (hu) |
HR (1) | HRP20160573T1 (hu) |
HU (1) | HUE029564T2 (hu) |
PL (1) | PL2516629T3 (hu) |
PT (1) | PT2516629T (hu) |
RS (1) | RS54933B1 (hu) |
SI (1) | SI2516629T1 (hu) |
SM (1) | SMT201600187B (hu) |
WO (1) | WO2011079073A2 (hu) |
ZA (1) | ZA201204192B (hu) |
Families Citing this family (9)
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US9273326B2 (en) | 2004-04-30 | 2016-03-01 | The Brigham And Women's Hospital, Inc. | Tetracycline-regulated gene expression in HSV-1 vectors |
US20080008686A1 (en) | 2006-07-10 | 2008-01-10 | The Brigham And Women's Hospital, Inc. | Tetracycline repressor regulated oncolytic viruses |
US8796440B2 (en) | 2009-08-31 | 2014-08-05 | The Brigham And Women's Hospital, Inc. | Promote system for regulatable gene expression in mammalian cells |
CN102666843B (zh) | 2009-12-21 | 2014-10-22 | 布里格海姆妇女医院公司 | 单纯疱疹病毒疫苗 |
ES2914081T3 (es) * | 2014-08-26 | 2022-06-07 | Hsf Pharmaceuticals | Agentes de inmunización y métodos de uso novedosos |
KR102227180B1 (ko) * | 2017-03-09 | 2021-03-12 | 시아먼 유니버시티 | 재조합 헤르페스 심플렉스 바이러스 및 이의 용도 |
US20200172928A1 (en) * | 2017-06-05 | 2020-06-04 | The Brigham And Women's Hospital, Inc. | Vero cell lines stably expressing hsv icp0 protein |
WO2019152821A1 (en) * | 2018-02-05 | 2019-08-08 | The Brigham And Women's Hospital, Inc. | Recombinant herpes simplex virus-2 expressing glycoprotein b and d antigens |
US20210324483A1 (en) | 2018-10-15 | 2021-10-21 | Regenxbio Inc. | Method for measuring the infectivity of replication defective viral vectors and viruses |
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GB9105992D0 (en) | 1991-03-21 | 1991-05-08 | Smithkline Beecham Biolog | Vaccine |
DE69328514T2 (de) * | 1992-03-13 | 2001-01-11 | Monsanto Co | Herstellung rekombinanter Proteine unter Verwendung von Herpes-Virus-Promotoren und VP16-Transaktivatoren |
US6183753B1 (en) * | 1994-08-09 | 2001-02-06 | Schering-Plough Veterinary Corp. | Recombinant chimeric virus and uses thereof |
US7223411B1 (en) | 1992-07-31 | 2007-05-29 | Dana-Farber Cancer Institute | Herpesvirus replication defective mutants |
CA2143326A1 (en) | 1992-08-26 | 1994-03-03 | Guerard Byrne | Tetracycline repressor-mediated binary regulation system for control of gene expression in transgenic animals |
US5589362A (en) | 1993-06-14 | 1996-12-31 | Basf Aktiengesellschaft | Tetracycline regulated transcriptional modulators with altered DNA binding specificities |
US5464758A (en) | 1993-06-14 | 1995-11-07 | Gossen; Manfred | Tight control of gene expression in eucaryotic cells by tetracycline-responsive promoters |
US5763217A (en) * | 1993-11-10 | 1998-06-09 | University Of British Columbia | Method of using, process of preparing and composition comprising recombinant herpesvirus vectors |
US5965440A (en) | 1995-12-07 | 1999-10-12 | The General Hospital Corporation | Controlled gene product delivery from a regulatable retroviral vector |
US5770414A (en) | 1996-02-20 | 1998-06-23 | The Regents Of The University Of California | Regulatable retrovirus system for genetic modification of cells |
US6261552B1 (en) | 1997-05-22 | 2001-07-17 | University Of Pittsburgh Of The Commonwealth System Of Higher Education | Herpes simplex virus vectors |
US5972650A (en) * | 1997-06-26 | 1999-10-26 | Brigham And Women's Hospital | Tetracycline repressor regulated mammalian cell transcription and viral replication switch |
US20040063094A1 (en) | 1998-05-20 | 2004-04-01 | Biovex Limited | Mutant herpes simplex viruses and uses thereof |
WO2001053505A2 (en) | 2000-01-21 | 2001-07-26 | Biovex Limited | Herpes virus strains for gene therapy |
EP1178111A1 (en) | 2000-08-03 | 2002-02-06 | Lohmann Animal Health GmbH & Co. KG | Vaccination against host cell-associated herpesviruses |
US6846670B2 (en) * | 2000-11-28 | 2005-01-25 | The University Of Chicago | Genetically engineered herpes virus for the treatment of cardiovascular disease |
US20040029229A1 (en) | 2002-05-20 | 2004-02-12 | Reeves Philip J. | High level protein expression system |
US20080299140A1 (en) * | 2002-05-24 | 2008-12-04 | The Regents Of The University Of California, | Immunogenic Composition and Peptide Sequences for Prevention and Treatment of an Hsv Condition |
CA2500270A1 (en) * | 2002-09-27 | 2004-04-08 | Powderject Research Limited | Nucleic acid constructs for gene expression |
US7335763B2 (en) | 2003-03-25 | 2008-02-26 | University Of Florida Research Foundation, Inc. | Herpesvirus ribozymes and vectors |
US20040229362A1 (en) * | 2003-05-15 | 2004-11-18 | Alberto Epstein | Method for producing non-pathogenic helper virus-free preparations of herpes virus amplicon vectors, the helper virus & the cells used in this method, the corresponding genetic tools, as well as the applications of these non-pathogenic amplicon vectors |
US9273326B2 (en) * | 2004-04-30 | 2016-03-01 | The Brigham And Women's Hospital, Inc. | Tetracycline-regulated gene expression in HSV-1 vectors |
US20080008686A1 (en) * | 2006-07-10 | 2008-01-10 | The Brigham And Women's Hospital, Inc. | Tetracycline repressor regulated oncolytic viruses |
US8796440B2 (en) * | 2009-08-31 | 2014-08-05 | The Brigham And Women's Hospital, Inc. | Promote system for regulatable gene expression in mammalian cells |
CN102666843B (zh) | 2009-12-21 | 2014-10-22 | 布里格海姆妇女医院公司 | 单纯疱疹病毒疫苗 |
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- 2010-12-20 EP EP10840033.4A patent/EP2516629B1/en active Active
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KR101747987B1 (ko) | 2017-06-15 |
HK1175807A1 (zh) | 2013-07-12 |
BR112012015172A2 (pt) | 2017-03-07 |
ZA201204192B (en) | 2013-02-27 |
CN102666843A (zh) | 2012-09-12 |
SI2516629T1 (sl) | 2016-10-28 |
PT2516629T (pt) | 2016-07-07 |
HRP20160573T1 (hr) | 2016-09-23 |
JP5845191B2 (ja) | 2016-01-20 |
US9408905B2 (en) | 2016-08-09 |
WO2011079073A2 (en) | 2011-06-30 |
US20120263752A1 (en) | 2012-10-18 |
RS54933B1 (sr) | 2016-10-31 |
WO2011079073A3 (en) | 2012-02-02 |
SMT201600187B (it) | 2016-11-10 |
US8809047B2 (en) | 2014-08-19 |
EP2516629A4 (en) | 2013-09-04 |
AU2010333749B2 (en) | 2015-07-30 |
DK2516629T3 (en) | 2016-07-04 |
EP2516629B1 (en) | 2016-04-13 |
PL2516629T3 (pl) | 2016-11-30 |
CN102666843B (zh) | 2014-10-22 |
RU2012131167A (ru) | 2014-01-27 |
AU2010333749A1 (en) | 2012-06-14 |
JP2013514784A (ja) | 2013-05-02 |
US20140314811A1 (en) | 2014-10-23 |
JP2015144619A (ja) | 2015-08-13 |
EP2516629A2 (en) | 2012-10-31 |
CA2783330A1 (en) | 2011-06-30 |
US20170028058A1 (en) | 2017-02-02 |
KR20120095450A (ko) | 2012-08-28 |
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