AU2011344652B2 - HLA-binding peptides derived from prostate-associated antigenic molecules and methods of use thereof - Google Patents
HLA-binding peptides derived from prostate-associated antigenic molecules and methods of use thereof Download PDFInfo
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- AU2011344652B2 AU2011344652B2 AU2011344652A AU2011344652A AU2011344652B2 AU 2011344652 B2 AU2011344652 B2 AU 2011344652B2 AU 2011344652 A AU2011344652 A AU 2011344652A AU 2011344652 A AU2011344652 A AU 2011344652A AU 2011344652 B2 AU2011344652 B2 AU 2011344652B2
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- A61K40/10—Cellular immunotherapy characterised by the cell type used
- A61K40/19—Dendritic cells
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- A61K40/41—Vertebrate antigens
- A61K40/42—Cancer antigens
- A61K40/4274—Prostate associated antigens e.g. Prostate stem cell antigen [PSCA]; Prostate carcinoma tumor antigen [PCTA]; Prostatic acid phosphatase [PAP]; Prostate-specific G-protein-coupled receptor [PSGR]
- A61K40/4276—Prostate specific membrane antigen [PSMA]
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4748—Tumour specific antigens; Tumour rejection antigen precursors [TRAP], e.g. MAGE
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- A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
- A61K2039/55511—Organic adjuvants
- A61K2039/55566—Emulsions, e.g. Freund's adjuvant, MF59
Landscapes
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Applications Claiming Priority (3)
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AUPCT/EP2010/069675 | 2010-12-14 | ||
PCT/EP2010/069675 WO2011073215A2 (en) | 2009-12-14 | 2010-12-14 | Hla-binding peptides derived from prostate-associated antigenic molecules and methods of use thereof |
PCT/EP2011/070024 WO2012079878A2 (en) | 2010-12-14 | 2011-11-14 | Hla-binding peptides derived from prostate-associated antigenic molecules and methods of use thereof |
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AU2011344652A1 AU2011344652A1 (en) | 2013-05-23 |
AU2011344652B2 true AU2011344652B2 (en) | 2015-11-19 |
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DE102013012432A1 (de) * | 2013-07-29 | 2015-01-29 | Eberhard Karls Universität Tübingen Medizinische Fakultät | Immuntherapie von Prostatakrebs |
MX384635B (es) * | 2014-04-16 | 2025-03-14 | Biosimilars Newco Ltd | Formulaciones de proteína estables que comprenden un exceso molar de sorbitol. |
EP3845557B1 (en) * | 2015-06-12 | 2023-08-02 | Lentigen Technology, Inc. | Method to treat cancer with engineered t-cells |
GB201513921D0 (en) | 2015-08-05 | 2015-09-23 | Immatics Biotechnologies Gmbh | Novel peptides and combination of peptides for use in immunotherapy against prostate cancer and other cancers |
GB201521746D0 (en) * | 2015-12-10 | 2016-01-27 | Immatics Biotechnologies Gmbh | Novel peptides and combination of peptides for use in immunotherapy against CLL and other cancers |
GB201602918D0 (en) * | 2016-02-19 | 2016-04-06 | Immatics Biotechnologies Gmbh | Novel peptides and combination of peptides for use in immunotherapy against NHL and other cancers |
GB201603987D0 (en) | 2016-03-08 | 2016-04-20 | Immatics Biotechnologies Gmbh | Uterine cancer treatments |
EP4317432A3 (en) | 2016-12-08 | 2024-04-17 | Immatics Biotechnologies GmbH | T cell receptors with improved pairing |
DE102016123893A1 (de) | 2016-12-08 | 2018-06-14 | Immatics Biotechnologies Gmbh | T-Zellrezeptoren mit verbesserter Bindung |
CN116693695A (zh) * | 2017-02-12 | 2023-09-05 | 百欧恩泰美国公司 | 基于hla的方法和组合物及其用途 |
KR102215578B1 (ko) * | 2019-03-28 | 2021-02-15 | 한국과학기술연구원 | 인간 백혈구 항원에 특이적으로 결합하는 펩타이드 및 이의 용도 |
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CA725596A (en) | 1960-08-26 | 1966-01-11 | J. Wretlind Arvid | Method of preparing intravenously injectable fat emulsions free from side reactions or complications |
US4897445A (en) | 1986-06-27 | 1990-01-30 | The Administrators Of The Tulane Educational Fund | Method for synthesizing a peptide containing a non-peptide bond |
AUPM322393A0 (en) | 1993-12-24 | 1994-01-27 | Austin Research Institute, The | Mucin carbohydrate compounds and their use in immunotherapy |
US5849589A (en) | 1996-03-11 | 1998-12-15 | Duke University | Culturing monocytes with IL-4, TNF-α and GM-CSF TO induce differentiation to dendric cells |
US6406705B1 (en) | 1997-03-10 | 2002-06-18 | University Of Iowa Research Foundation | Use of nucleic acids containing unmethylated CpG dinucleotide as an adjuvant |
JP2003521245A (ja) * | 1999-12-21 | 2003-07-15 | エピミューン, インコーポレイテッド | ペプチドおよび核酸組成物を使用する、前立腺癌抗原に対する細胞性免疫応答の誘導 |
US6436703B1 (en) * | 2000-03-31 | 2002-08-20 | Hyseq, Inc. | Nucleic acids and polypeptides |
US20020081680A1 (en) * | 2000-04-17 | 2002-06-27 | Jiangchun Xu | Compositions and methods for the therapy and diagnosis of prostate cancer |
US7892559B2 (en) | 2002-01-30 | 2011-02-22 | Survac Aps | Survivin-derived peptides and use thereof |
AU2003217421A1 (en) * | 2002-02-19 | 2003-09-09 | Idec Pharmaceuticals Corporation | Prostate specific genes and the use thereof in design or therapeutics |
US7906620B2 (en) * | 2002-08-16 | 2011-03-15 | Yeda Research And Development Co. Ltd. | Tumor associated antigen, peptides thereof, and use of same as anti-tumor vaccines |
US20060205934A1 (en) * | 2002-12-05 | 2006-09-14 | Macina Roberto A | Compositions, splice variants and methods relating to breast specific genes and proteins |
WO2005033265A2 (en) * | 2003-04-25 | 2005-04-14 | Epimmune Inc. | Optimized multi-epitope constructs and uses thereof |
WO2006023598A2 (en) * | 2004-08-19 | 2006-03-02 | University Of Maryland, Baltimore | Prostate-specific antigen-derived mhc class ii-restricted peptides and their use in vaccines to treat or prevent prostate cancer |
DE602004019215D1 (de) | 2004-10-02 | 2009-03-12 | Immatics Biotechnologies Gmbh | Immunogene T-Helfer Epitope von menschlichen Tumorantigenen und deren Verwendung in immunotherapeutischen Methoden |
EP1806358B1 (en) | 2005-09-05 | 2010-03-17 | Immatics Biotechnologies GmbH | Tumor-associated peptides binding promiscuously to human leukocyte antigen (HLA) class II molecules |
PT2113253E (pt) * | 2008-04-30 | 2010-06-15 | Immatics Biotechnologies Gmbh | Formulações novas de peptídeos associados a tumores que se ligam a moléculas de classe i ou ii do antígeno leucocitário humano (hla) para vacinas |
EP2119726B2 (en) * | 2008-05-14 | 2017-11-29 | Immatics Biotechnologies GmbH | Novel and powerful MHC-class II peptides derived from survivin and neurocan |
DK2172211T3 (en) * | 2008-10-01 | 2015-02-16 | Immatics Biotechnologies Gmbh | Composition of tumor-associated peptides and related anti-cancer vaccine for the treatment of glioblastoma (GBM) and other cancers |
-
2011
- 2011-11-14 CN CN201180059274.2A patent/CN103547283A/zh active Pending
- 2011-11-14 MX MX2013006758A patent/MX2013006758A/es unknown
- 2011-11-14 WO PCT/EP2011/070024 patent/WO2012079878A2/en active Application Filing
- 2011-11-14 JP JP2013543601A patent/JP6032853B2/ja not_active Expired - Fee Related
- 2011-11-14 CA CA2821582A patent/CA2821582A1/en not_active Abandoned
- 2011-11-14 NZ NZ60991611A patent/NZ609916A/en not_active IP Right Cessation
- 2011-11-14 KR KR1020137018147A patent/KR20130126671A/ko not_active Withdrawn
- 2011-11-14 AU AU2011344652A patent/AU2011344652B2/en not_active Ceased
- 2011-11-14 SG SG2013045737A patent/SG191154A1/en unknown
Non-Patent Citations (1)
Title |
---|
KIESSLING ET AL: "Advances in Specific Immunotherapy for Prostate Cancer" , EUROPEAN UROLOGY, ELSEVIER BV, NL, vol. 53, no. 4, 26 November 2007 (2007-11-26). pages 694-708, * |
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CA2821582A1 (en) | 2012-06-21 |
SG191154A1 (en) | 2013-07-31 |
NZ609916A (en) | 2015-03-27 |
AU2011344652A1 (en) | 2013-05-23 |
CN103547283A (zh) | 2014-01-29 |
JP2014502961A (ja) | 2014-02-06 |
JP6032853B2 (ja) | 2016-11-30 |
WO2012079878A2 (en) | 2012-06-21 |
MX2013006758A (es) | 2013-08-01 |
WO2012079878A3 (en) | 2012-08-09 |
KR20130126671A (ko) | 2013-11-20 |
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