CA2296366A1 - Traitement des leucocytes, compositions leucocytaires, et leur procede d'utilisation - Google Patents
Traitement des leucocytes, compositions leucocytaires, et leur procede d'utilisation Download PDFInfo
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- CA2296366A1 CA2296366A1 CA002296366A CA2296366A CA2296366A1 CA 2296366 A1 CA2296366 A1 CA 2296366A1 CA 002296366 A CA002296366 A CA 002296366A CA 2296366 A CA2296366 A CA 2296366A CA 2296366 A1 CA2296366 A1 CA 2296366A1
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/28—Bone marrow; Haematopoietic stem cells; Mesenchymal stem cells of any origin, e.g. adipose-derived stem cells
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K40/10—Cellular immunotherapy characterised by the cell type used
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K40/20—Cellular immunotherapy characterised by the effect or the function of the cells
- A61K40/22—Immunosuppressive or immunotolerising
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- A61K40/40—Cellular immunotherapy characterised by antigens that are targeted or presented by cells of the immune system
- A61K40/41—Vertebrate antigens
- A61K40/418—Antigens related to induction of tolerance to non-self
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- A61K40/40—Cellular immunotherapy characterised by antigens that are targeted or presented by cells of the immune system
- A61K40/41—Vertebrate antigens
- A61K40/42—Cancer antigens
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues
- C12N5/0602—Vertebrate cells
- C12N5/0634—Cells from the blood or the immune system
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- A61K2239/31—Indexing codes associated with cellular immunotherapy of group A61K40/00 characterized by the route of administration
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K2239/38—Indexing codes associated with cellular immunotherapy of group A61K40/00 characterised by the dose, timing or administration schedule
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- A61K2239/00—Indexing codes associated with cellular immunotherapy of group A61K40/00
- A61K2239/46—Indexing codes associated with cellular immunotherapy of group A61K40/00 characterised by the cancer treated
- A61K2239/48—Blood cells, e.g. leukemia or lymphoma
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
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- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
L'invention concerne des méthodes et des compositions permettant de traiter des leucocytes de manière à stopper leur prolifération et à les rendre incapables de déclencher des réactions du greffon contre l'hôte, mais capables d'améliorer la greffe de cellules de donneurs allogéniques et d'accélérer la destruction de cellules malades ou d'agents pathogènes. L'invention concerne également des compositions leucocytaires et des méthodes d'utilisation de ces compositions visant à atténuer des maladies, à accélérer plusieurs types de reconstitution du système immunitaire et d'immunothérapies, et à améliorer la greffe de cellules de donneurs allogéniques.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5359997P | 1997-07-21 | 1997-07-21 | |
| US60/053,599 | 1997-07-21 | ||
| US11970798A | 1998-07-20 | 1998-07-20 | |
| US09/119,707 | 1998-07-20 | ||
| PCT/US1998/015067 WO1999003976A2 (fr) | 1997-07-21 | 1998-07-21 | Traitement des leucocytes, compositions leucocytaires, et leur procede d'utilisation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2296366A1 true CA2296366A1 (fr) | 1999-01-28 |
Family
ID=26732039
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002296366A Abandoned CA2296366A1 (fr) | 1997-07-21 | 1998-07-21 | Traitement des leucocytes, compositions leucocytaires, et leur procede d'utilisation |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1005531A2 (fr) |
| JP (1) | JP2003520563A (fr) |
| CN (1) | CN1270630A (fr) |
| AU (1) | AU748074B2 (fr) |
| CA (1) | CA2296366A1 (fr) |
| WO (1) | WO1999003976A2 (fr) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU781855B2 (en) * | 1999-10-05 | 2005-06-16 | Hopital Maisonneuve-Rosemont | Rhodamine derivatives for photodynamic diagnosis and treatment |
| US8409564B2 (en) | 1999-10-05 | 2013-04-02 | Universite De Montreal | Rhodamine derivatives for photodynamic diagnosis and treatment |
| AU2002218019A1 (en) * | 2000-11-03 | 2002-05-15 | Nexell Therapeutics Inc. | Methods for depleting and isolating alloreactive and antigen-reactive t cells from hematopoietic donor cells |
| DE10112851C1 (de) | 2001-03-16 | 2002-10-10 | Gsf Forschungszentrum Umwelt | Semi-allogene Antitumor-Vakzine mit HLA-haplo-identischen Antigen-präsentierenden Zellen |
| KR101192652B1 (ko) | 2003-02-06 | 2012-10-19 | 앤저 테라퓨틱스 인코퍼레이티드 | 비포식 세포로의 침투가 약화된 리스테리아, 리스테리아를 포함하는 백신, 및 그것의 사용방법 |
| US7695725B2 (en) | 2003-02-06 | 2010-04-13 | Aduro Biotech | Modified free-living microbes, vaccine compositions and methods of use thereof |
| KR101173871B1 (ko) | 2003-02-06 | 2012-08-16 | 앤저 테라퓨틱스 인코퍼레이티드 | 변형된 독립생존 미생물, 백신 조성물 및 그것의 사용방법 |
| DK2352756T3 (da) | 2008-11-24 | 2012-12-03 | Helmholtz Zentrum Muenchen | Højaffin T-cellereceptor og anvendelse af denne |
| DE102011085695A1 (de) * | 2011-11-03 | 2013-05-08 | Jörg Pohl | Einmalig dosierte Oxazaphosphorine zur Therapie von Krankheiten |
| US20130252227A1 (en) * | 2012-03-20 | 2013-09-26 | Fenwal, Inc. | Apparatus and Method for Providing Cryopreserved ECP-Treated Mononuclear Cells |
| US20190224494A1 (en) * | 2012-03-20 | 2019-07-25 | Fenwal, Inc. | Apparatus and method for batch photoactivation of mononuclear cells with cryopreservation |
| WO2016073381A1 (fr) * | 2014-11-03 | 2016-05-12 | Cerus Corporation | Compositions et procédés pour thérapies par cellules car-t améliorées |
| EP3058957A1 (fr) * | 2015-02-19 | 2016-08-24 | Kiadis Pharma Intellectual Property BV | Traitement photodynamique amélioré et produit ainsi obtenu |
| CN104788373A (zh) * | 2015-05-06 | 2015-07-22 | 武汉大学 | 化合物s-303盐酸盐的合成方法 |
| EP3313418B1 (fr) | 2015-06-26 | 2024-03-13 | Cerus Corporation | Compositions de cryoprécipités et leurs procédés de préparation |
| US10898522B2 (en) | 2015-08-19 | 2021-01-26 | Children's Research Institute, Children's National Medical Center | Compositions and methods for treating graft versus host disease |
| CA3003097A1 (fr) | 2015-10-23 | 2017-04-27 | Cerus Corporation | Compositions de plasma et leurs procedes d'utilisation |
| US20190369087A1 (en) | 2016-12-23 | 2019-12-05 | Cerus Corporation | Systems and methods for testing and screening using compound bound substrates |
| CA3055203A1 (fr) | 2017-03-03 | 2018-09-07 | Cerus Corporation | Kits et methodes de preparation de compositions de plaquettes inactivees par des agents pathogenes |
| US11679193B2 (en) | 2017-12-20 | 2023-06-20 | Fenwal, Inc. | System and method of collecting and infusing an apoptotic white blood cell component and a transplant component |
| AU2018395525B2 (en) | 2017-12-29 | 2023-09-14 | Cerus Corporation | Systems and methods for treating biological fluids |
| FR3082730B1 (fr) | 2018-06-21 | 2022-04-22 | Med Inn Pharma | Methode de resolution de l'inflammation pro-tumorale a l'aide d'une preparation pharmaceutique |
| CN109337758A (zh) * | 2018-11-30 | 2019-02-15 | 广西科技大学 | 一种基于紫外线强化dna与黄曲霉毒素嵌合作用的油脂黄曲霉毒素俘获消除方法 |
| JP7571063B2 (ja) | 2019-06-22 | 2024-10-22 | シーラス コーポレイション | 生物学的流体の処理を実施するシステム及び方法 |
| US12011510B2 (en) | 2019-06-22 | 2024-06-18 | Cerus Corporation | Biological fluid treatment systems |
| CN114269394A (zh) | 2019-06-28 | 2022-04-01 | 塞鲁斯公司 | 用于实现生物流体处理装置的系统和方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4838852A (en) * | 1987-03-27 | 1989-06-13 | Therakos, Inc. | Active specific immune suppression |
| US5651993A (en) * | 1992-11-18 | 1997-07-29 | Yale University | Specific immune system modulation |
| WO1996039820A1 (fr) * | 1995-06-07 | 1996-12-19 | Cerus Corporation | Procedes d'inactivation de leucocytes et d'inhibition de la production de cytokines dans des produits sanguins |
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- 1998-07-21 EP EP98936943A patent/EP1005531A2/fr not_active Withdrawn
- 1998-07-21 JP JP2000503182A patent/JP2003520563A/ja not_active Withdrawn
- 1998-07-21 CA CA002296366A patent/CA2296366A1/fr not_active Abandoned
- 1998-07-21 CN CN98809097A patent/CN1270630A/zh active Pending
- 1998-07-21 WO PCT/US1998/015067 patent/WO1999003976A2/fr not_active Ceased
- 1998-07-21 AU AU85776/98A patent/AU748074B2/en not_active Ceased
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| Publication number | Publication date |
|---|---|
| JP2003520563A (ja) | 2003-07-08 |
| CN1270630A (zh) | 2000-10-18 |
| WO1999003976A2 (fr) | 1999-01-28 |
| WO1999003976A3 (fr) | 1999-05-27 |
| EP1005531A2 (fr) | 2000-06-07 |
| AU8577698A (en) | 1999-02-10 |
| AU748074B2 (en) | 2002-05-30 |
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