RU2010116271A - Ангиогенные клетки из плацентарного перфузата человека - Google Patents
Ангиогенные клетки из плацентарного перфузата человека Download PDFInfo
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- 230000003169 placental effect Effects 0.000 title claims abstract 28
- 230000002491 angiogenic effect Effects 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract 40
- 102100031573 Hematopoietic progenitor cell antigen CD34 Human genes 0.000 claims abstract 34
- 101000777663 Homo sapiens Hematopoietic progenitor cell antigen CD34 Proteins 0.000 claims abstract 34
- 210000004700 fetal blood Anatomy 0.000 claims abstract 8
- 230000010412 perfusion Effects 0.000 claims abstract 7
- 210000002826 placenta Anatomy 0.000 claims abstract 6
- 102100031650 C-X-C chemokine receptor type 4 Human genes 0.000 claims abstract 5
- 101000922348 Homo sapiens C-X-C chemokine receptor type 4 Proteins 0.000 claims abstract 5
- 102100024616 Platelet endothelial cell adhesion molecule Human genes 0.000 claims abstract 5
- 108091008605 VEGF receptors Proteins 0.000 claims abstract 5
- 102100033177 Vascular endothelial growth factor receptor 2 Human genes 0.000 claims abstract 5
- 210000004369 blood Anatomy 0.000 claims abstract 3
- 239000008280 blood Substances 0.000 claims abstract 3
- 210000001185 bone marrow Anatomy 0.000 claims abstract 3
- 239000011159 matrix material Substances 0.000 claims abstract 3
- 210000005259 peripheral blood Anatomy 0.000 claims abstract 3
- 239000011886 peripheral blood Substances 0.000 claims abstract 3
- 102000005741 Metalloproteases Human genes 0.000 claims abstract 2
- 108010006035 Metalloproteases Proteins 0.000 claims abstract 2
- 102000004887 Transforming Growth Factor beta Human genes 0.000 claims abstract 2
- 108090001012 Transforming Growth Factor beta Proteins 0.000 claims abstract 2
- 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 claims abstract 2
- 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 claims abstract 2
- 230000015572 biosynthetic process Effects 0.000 claims abstract 2
- 210000004204 blood vessel Anatomy 0.000 claims abstract 2
- 238000000338 in vitro Methods 0.000 claims abstract 2
- 238000001727 in vivo Methods 0.000 claims abstract 2
- ZRKFYGHZFMAOKI-QMGMOQQFSA-N tgfbeta Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CCSC)C(C)C)[C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N1[C@@H](CCC1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O)C1=CC=C(O)C=C1 ZRKFYGHZFMAOKI-QMGMOQQFSA-N 0.000 claims abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 6
- 101000738771 Homo sapiens Receptor-type tyrosine-protein phosphatase C Proteins 0.000 claims 5
- 102100037422 Receptor-type tyrosine-protein phosphatase C Human genes 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 3
- 208000035475 disorder Diseases 0.000 claims 3
- 230000001575 pathological effect Effects 0.000 claims 3
- 208000020446 Cardiac disease Diseases 0.000 claims 1
- 206010007558 Cardiac failure chronic Diseases 0.000 claims 1
- 206010007559 Cardiac failure congestive Diseases 0.000 claims 1
- 208000031229 Cardiomyopathies Diseases 0.000 claims 1
- 206010019280 Heart failures Diseases 0.000 claims 1
- 208000018262 Peripheral vascular disease Diseases 0.000 claims 1
- 208000014888 Vascular hypertensive disease Diseases 0.000 claims 1
- 230000001154 acute effect Effects 0.000 claims 1
- 210000001367 artery Anatomy 0.000 claims 1
- 230000000747 cardiac effect Effects 0.000 claims 1
- 230000001684 chronic effect Effects 0.000 claims 1
- 230000002526 effect on cardiovascular system Effects 0.000 claims 1
- 208000019622 heart disease Diseases 0.000 claims 1
- 208000028867 ischemia Diseases 0.000 claims 1
- 208000010125 myocardial infarction Diseases 0.000 claims 1
- 230000002093 peripheral effect Effects 0.000 claims 1
- 230000002685 pulmonary effect Effects 0.000 claims 1
- 208000004124 rheumatic heart disease Diseases 0.000 claims 1
- 208000019553 vascular disease Diseases 0.000 claims 1
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- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/48—Reproductive organs
- A61K35/50—Placenta; Placental stem cells; Amniotic fluid; Amnion; Amniotic stem cells
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- C12N5/06—Animal cells or tissues; Human cells or tissues
- C12N5/0602—Vertebrate cells
- C12N5/069—Vascular Endothelial cells
- C12N5/0692—Stem cells; Progenitor cells; Precursor cells
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Abstract
1. Способ формирования сосудов из популяции клеток плацентарного перфузата, включающий приведение в контакт указанной популяции клеток в условиях, которые способствуют формированию сосудов. ! 2. Способ по п.1, где указанная популяция клеток плацентарного перфузата представляет собой все нуклеарные клетки плацентарного перфузата. ! 3. Способ по п.1, где указанное приведение в контакт включает приведение в контакт указанных клеток с VEGF (50-200 нг/мл), TGF-β (1-5 нг/мл), FGF (10-50 нг/мл), а также одной или нескольких матриксных металлопротеаз (1-3 единицы/мл каждая). ! 4. Способ по п.1, где указанное приведение в контакт осуществляют in vitro. ! 5. Способ по п.1, где указанное приведение в контакт осуществляют in vivo. ! 6. Способ по п.1, где указанная популяция клеток плацентарного перфузата включает клетки плацентарного перфузата, выделенные при перфузии одной плаценты. ! 7. Способ по п.6, где указанные клетки плацентарного перфузата представляют собой клетки CD34+. ! 8. Способ по п.7, где указанные клетки CD34+ представляют собой клетки CD34+CD45-. ! 9. Способ по п.6 или 7, где указанные клетки CD34+ или клетки CD34+CD45- экспрессируют более высокий уровень по меньшей мере одного из CD31, CXCR4 или VEGFR по сравнению с эквивалентным числом клеток CD34+ пуповинной крови. ! 10. Способ по п.1, где указанная популяция клеток плацентарного перфузата включает выделенные клетки CD34+, выделенные не из указанного перфузата. ! 11. Способ по п.10, где указанные клетки CD34+ выделяют из плаценты. ! 12. Способ по п.10, где указанные клетки CD34+ выделяют из пуповинной крови, плацентарной крови, периферической крови или костного мозга. ! 13. Способ по п.10, где указанные клетки CD34+ экспрессируют более высокий ур�
Claims (27)
1. Способ формирования сосудов из популяции клеток плацентарного перфузата, включающий приведение в контакт указанной популяции клеток в условиях, которые способствуют формированию сосудов.
2. Способ по п.1, где указанная популяция клеток плацентарного перфузата представляет собой все нуклеарные клетки плацентарного перфузата.
3. Способ по п.1, где указанное приведение в контакт включает приведение в контакт указанных клеток с VEGF (50-200 нг/мл), TGF-β (1-5 нг/мл), FGF (10-50 нг/мл), а также одной или нескольких матриксных металлопротеаз (1-3 единицы/мл каждая).
4. Способ по п.1, где указанное приведение в контакт осуществляют in vitro.
5. Способ по п.1, где указанное приведение в контакт осуществляют in vivo.
6. Способ по п.1, где указанная популяция клеток плацентарного перфузата включает клетки плацентарного перфузата, выделенные при перфузии одной плаценты.
7. Способ по п.6, где указанные клетки плацентарного перфузата представляют собой клетки CD34+.
8. Способ по п.7, где указанные клетки CD34+ представляют собой клетки CD34+CD45-.
9. Способ по п.6 или 7, где указанные клетки CD34+ или клетки CD34+CD45- экспрессируют более высокий уровень по меньшей мере одного из CD31, CXCR4 или VEGFR по сравнению с эквивалентным числом клеток CD34+ пуповинной крови.
10. Способ по п.1, где указанная популяция клеток плацентарного перфузата включает выделенные клетки CD34+, выделенные не из указанного перфузата.
11. Способ по п.10, где указанные клетки CD34+ выделяют из плаценты.
12. Способ по п.10, где указанные клетки CD34+ выделяют из пуповинной крови, плацентарной крови, периферической крови или костного мозга.
13. Способ по п.10, где указанные клетки CD34+ экспрессируют более высокий уровень CD31, CXCR4 или VEGFR по сравнению с эквивалентным числом клеток CD34+ пуповинной крови.
14. Способ по п.10, где указанные клетки CD34+ представляют собой клетки CD34+CD45-.
15. Способ лечения индивидуума, страдающего сердечным или сосудистым заболеванием, нарушением, патологическим состоянием или недостаточностью, включающий введение плацентарного перфузата человека или клеток плацентарного перфузата человека указанному индивидууму в количестве, достаточном для лечения указанного заболевания, нарушения, патологического состояния или недостаточности.
16. Способ по п.15, где указанное заболевание, нарушение, патологическое состояние или недостаточность представляет собой заболевание периферических сосудов, острый или хронический инфаркт миокарда, кардиомиопатию, застойную или хроническую сердечную недостаточность, сердечно-сосудистую ишемию, легочное сосудистое гипертензивное заболевание, заболевание периферических артерий или ревматический порок сердца.
17. Способ по п.15, где указанные клетки плацентарного перфузата представляют собой все нуклеарные клетки плацентарного перфузата.
18. Способ по п.15, где указанная популяция клеток плацентарного перфузата включает клетки плацентарного перфузата, выделенные при перфузии одной плаценты.
19. Способ по п.18, где указанные клетки плацентарного перфузата представляют собой клетки CD34+.
20. Способ по п.19, где указанные клетки CD34+ представляют собой клетки CD34+CD45-.
21. Способ по п.19 или 20, где указанные клетки CD34+ или клетки CD34+CD45- экспрессируют более высокий уровень по меньшей мере одного из CD31, CXCR4 или VEGFR по сравнению с эквивалентным числом клеток CD34+ пуповинной крови.
22. Способ по п.15, где указанная популяция клеток плацентарного перфузата включает выделенные клетки CD34+, выделенные не из указанного перфузата.
23. Способ по п.22, где указанные клетки CD34+ выделяют из плаценты.
24. Способ по п.22, где указанные клетки CD34+ выделяют из пуповинной крови, плацентарной крови, периферической крови или костного мозга.
25. Способ по п.22, где указанные клетки CD34+ экспрессируют более высокий уровень CD31, CXCR4 или VEGFR по сравнению с эквивалентным числом клеток CD34+ пуповинной крови.
26. Способ по п.15, где указанные клетки плацентарного перфузата вводят на клеточном каркасе или матрице.
27. Способ по п.15, где указанные клетки плацентарного перфузата вводят внутривенно.
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US99567907P | 2007-09-26 | 2007-09-26 | |
US60/995,679 | 2007-09-26 |
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US (1) | US20090104164A1 (ru) |
EP (1) | EP2205719A1 (ru) |
JP (6) | JP5703493B2 (ru) |
KR (9) | KR20190050867A (ru) |
CN (1) | CN101978045A (ru) |
AU (1) | AU2008305516A1 (ru) |
BR (1) | BRPI0818191A8 (ru) |
CA (1) | CA2700613C (ru) |
IL (4) | IL204762A0 (ru) |
MX (1) | MX2010003217A (ru) |
RU (1) | RU2010116271A (ru) |
WO (1) | WO2009042201A1 (ru) |
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US20080152629A1 (en) * | 2000-12-06 | 2008-06-26 | James Edinger | Placental stem cell populations |
CA2678490A1 (en) | 2000-12-06 | 2002-06-13 | Robert J. Hariri | Isolated placental perfusate and placental cells isolated therefrom |
US7311905B2 (en) * | 2002-02-13 | 2007-12-25 | Anthrogenesis Corporation | Embryonic-like stem cells derived from post-partum mammalian placenta, and uses and methods of treatment using said cells |
KR101132545B1 (ko) | 2001-02-14 | 2012-04-02 | 안트로제네시스 코포레이션 | 산후 포유류의 태반, 이의 용도 및 태반 줄기세포 |
US7498171B2 (en) * | 2002-04-12 | 2009-03-03 | Anthrogenesis Corporation | Modulation of stem and progenitor cell differentiation, assays, and uses thereof |
BR0316695A (pt) * | 2002-11-26 | 2005-10-18 | Anthrogenesis Corp | Unidade citoterapêutica, kit para tratamento, método de tratamento de uma enfermidade, biblioteca de unidades citoterapêuticas e método de tratamento de um paciente |
GB0321337D0 (en) * | 2003-09-11 | 2003-10-15 | Massone Mobile Advertising Sys | Method and system for distributing advertisements |
BRPI0509141A (pt) * | 2004-03-26 | 2007-09-04 | Celgene Corp | método para manter um registro de células-tronco, produto de programa de computação para uso junto com um sistema de computador, sistema de computador, e, meio legìvel por computador |
PE20070771A1 (es) * | 2005-10-13 | 2007-08-11 | Anthrogenesis Corp | Inmunomodulacion mediante el uso de celulas madres de la placenta |
ZA200803929B (en) * | 2005-10-13 | 2009-08-26 | Anthrogenesis Corp | Production of oligodendrocytes from placenta-derived stem cells |
ZA200804717B (en) | 2005-12-29 | 2010-02-24 | Anthrogenesis Corp | Improved composition for collecting and preserving a placental stem cells and methods of using the composition |
CN101389754A (zh) * | 2005-12-29 | 2009-03-18 | 人类起源公司 | 胎盘干细胞和第二来源干细胞的联合培养 |
ES2708933T3 (es) | 2005-12-29 | 2019-04-12 | Celularity Inc | Poblaciones de células madre placentarias |
US7993918B2 (en) | 2006-08-04 | 2011-08-09 | Anthrogenesis Corporation | Tumor suppression using placental stem cells |
PT2084268T (pt) * | 2006-10-23 | 2019-01-28 | Celularity Inc | Métodos e composições para o tratamento de defeitos ósseos com populações de células placentárias |
RS52921B (en) | 2007-02-12 | 2014-02-28 | Anthrogenesis Corporation | TREATMENT OF INFLAMMATORY DISEASES USING PLACENTAL CELL CELLS |
EP2129775A1 (en) * | 2007-02-12 | 2009-12-09 | Anthrogenesis Corporation | Hepatocytes and chondrocytes from adherent placental stem cells; and cd34+, cd45- placental stem cell-enriched cell populations |
US9200253B1 (en) | 2007-08-06 | 2015-12-01 | Anthrogenesis Corporation | Method of producing erythrocytes |
KR20190050867A (ko) * | 2007-09-26 | 2019-05-13 | 안트로제네시스 코포레이션 | 인간 태반 관류액으로부터의 혈관형성 세포 |
ES2530995T3 (es) | 2007-09-28 | 2015-03-09 | Anthrogenesis Corp | Supresión de tumor usando perfusato placentario humano y células asesinas naturales intermediarias que provienen de placenta humana |
EP2329012B1 (en) * | 2008-08-20 | 2020-05-20 | Celularity, Inc. | Treatment of stroke using isolated placental cells |
NZ591292A (en) | 2008-08-20 | 2012-10-26 | Anthrogenesis Corp | Improved cell composition and methods of making the same |
CA2734446C (en) | 2008-08-22 | 2017-06-20 | Anthrogenesis Corporation | Methods and compositions for treatment of bone defects with placental cell populations |
JP5869342B2 (ja) | 2008-11-19 | 2016-02-24 | アンスロジェネシス コーポレーション | 羊膜由来接着細胞 |
NZ597436A (en) * | 2009-07-02 | 2014-08-29 | Anthrogenesis Corp | Method of producing erythrocytes without feeder cells |
US9163212B2 (en) * | 2010-01-25 | 2015-10-20 | Warsaw Orthopedic, Inc. | Osteogenic cell delivery matrix |
EP3284818B1 (en) | 2010-01-26 | 2022-03-09 | Celularity Inc. | Treatment of bone-related cancers using placental stem cells |
EP3345998A1 (en) | 2010-02-18 | 2018-07-11 | Osiris Therapeutics, Inc. | Immunocompatible chorionic membrane products |
TW202011974A (zh) | 2010-04-07 | 2020-04-01 | 美商安瑟吉納西斯公司 | 利用胎盤幹細胞之血管新生 |
TW201138792A (en) | 2010-04-08 | 2011-11-16 | Anthrogenesis Corp | Treatment of sarcoidosis using placental stem cells |
US9352003B1 (en) | 2010-05-14 | 2016-05-31 | Musculoskeletal Transplant Foundation | Tissue-derived tissuegenic implants, and methods of fabricating and using same |
US10130736B1 (en) | 2010-05-14 | 2018-11-20 | Musculoskeletal Transplant Foundation | Tissue-derived tissuegenic implants, and methods of fabricating and using same |
US8883210B1 (en) | 2010-05-14 | 2014-11-11 | Musculoskeletal Transplant Foundation | Tissue-derived tissuegenic implants, and methods of fabricating and using same |
WO2012009422A1 (en) | 2010-07-13 | 2012-01-19 | Anthrogenesis Corporation | Methods of generating natural killer cells |
AR093183A1 (es) | 2010-12-31 | 2015-05-27 | Anthrogenesis Corp | Aumento de la potencia de celulas madre de placenta usando moleculas de arn moduladoras |
TWI602570B (zh) | 2011-06-01 | 2017-10-21 | 安瑟吉納西斯公司 | 使用胎盤幹細胞之疼痛治療 |
WO2013055476A1 (en) | 2011-09-09 | 2013-04-18 | Anthrogenesis Corporation | Treatment of amyotrophic lateral sclerosis using placental stem cells |
AU2013204922B2 (en) | 2012-12-20 | 2015-05-14 | Celgene Corporation | Chimeric antigen receptors |
WO2014123879A1 (en) | 2013-02-05 | 2014-08-14 | Anthrogenesis Corporation | Natural killer cells from placenta |
JP6571537B2 (ja) * | 2013-03-13 | 2019-09-04 | ザ ユニバーシティー オブ クイーンズランド | 療法および予防のための細胞を単離する方法 |
US10238690B2 (en) | 2013-03-15 | 2019-03-26 | Celgene Corporation | Modified T lymphocytes comprising an inducible caspase and methods of apoptosis |
JP2016516091A (ja) | 2013-04-02 | 2016-06-02 | ユニバーシティ オブ フロリダ リサーチ ファンデーション インコーポレーティッド | 血管新生の誘導および調節のための組成物および方法、ならびに血管新生調節因子を同定する方法およびアッセイ |
EP3068432A4 (en) * | 2013-11-15 | 2017-04-19 | Anthrogenesis Corporation | Compositions comprising human placental perfusate cells, subpopulations thereof, and their uses |
CN103756965B (zh) * | 2014-01-27 | 2016-04-06 | 山东省齐鲁干细胞工程有限公司 | 一种从胎盘中灌洗造血干细胞的方法 |
CN104152405B (zh) * | 2014-08-15 | 2016-06-29 | 博雅干细胞科技有限公司 | 从胎盘中分离提取造血干细胞的方法 |
CA3177726A1 (en) | 2015-05-21 | 2016-11-24 | Musculoskeletal Transplant Foundation | Modified demineralized cortical bone fibers |
US20180216065A1 (en) * | 2015-07-20 | 2018-08-02 | The Catholic University Of Korea Industry-Academic Cooperation Foundation | Method for Inducing Differentiation of Myeloid-Derived Suppressor Cells from Cord - Blood CD34 Positive Cells and Proliferating Same, and use of Myeloid-Derived |
ES2914692T3 (es) * | 2015-08-12 | 2022-06-15 | Cha Biotech Co Ltd | Células madre adhesivas derivadas de cordón umbilical mejoradas, método de preparación para las mismas, y uso de las mismas |
MX2019006514A (es) * | 2016-12-05 | 2019-10-30 | Celularity Inc | Tratamiento de linfedema y afecciones relacionadas a través del uso de las células adherentes placentarias. |
CN107058224B (zh) * | 2017-02-10 | 2020-08-21 | 广东唯泰生物科技有限公司 | 一种以胎盘为来源的造血干细胞提取及冻存方法 |
KR20210111762A (ko) | 2018-11-30 | 2021-09-13 | 셀룰래리티 인코포레이티드 | 신규 방향족 화합물을 사용한 자연 살해 세포 및 ilc3 세포의 증식 |
CN109652372A (zh) * | 2019-01-09 | 2019-04-19 | 陕西九州细胞基因工程有限公司 | 一种人胎盘组织源造血干细胞的快速分离、制备方法 |
JP6977969B2 (ja) * | 2019-03-22 | 2021-12-08 | 株式会社ガイアバイオメディシン | 免疫細胞提供システム |
WO2020252464A1 (en) | 2019-06-14 | 2020-12-17 | Celularity Inc. | Populations of natural killer cells for treating cancers |
US20220273716A1 (en) | 2019-07-25 | 2022-09-01 | Celularity Inc. | Populations of natural killer cells comprising a cd38 chimeric antigen receptor |
WO2021022229A1 (en) | 2019-07-31 | 2021-02-04 | Celularity Inc. | Populations of natural killer cells comprising a cleavage resistant cd16 |
WO2021113849A1 (en) | 2019-12-05 | 2021-06-10 | Celularity Inc. | Her2+ cancer treatment with populations of natural killer cells comprising a cleavage resistant cd16 |
US20220000919A1 (en) | 2020-01-29 | 2022-01-06 | Celularity Inc. | Placental derived natural killer cells for treatment of coronavirus infections |
WO2023278628A1 (en) | 2021-06-29 | 2023-01-05 | Celularity Inc. | Human placental hematopoietic stem cell derived natural killer cells in acute myeloid leukemia (aml) remission with minimal residual disease (mrd) or relapsed/refractory aml |
WO2023010123A1 (en) | 2021-07-29 | 2023-02-02 | Celularity Inc. | Placenta-dervied nk cells as a senolytic for therapeutic and other uses |
WO2023137344A1 (en) | 2022-01-11 | 2023-07-20 | Celularity Inc. | Cleavage resistant cd16 constructs and uses thereof |
Family Cites Families (99)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3862002A (en) * | 1962-05-08 | 1975-01-21 | Sanfar Lab Inc | Production of physiologically active placental substances |
US5863531A (en) * | 1986-04-18 | 1999-01-26 | Advanced Tissue Sciences, Inc. | In vitro preparation of tubular tissue structures by stromal cell culture on a three-dimensional framework |
US5192553A (en) * | 1987-11-12 | 1993-03-09 | Biocyte Corporation | Isolation and preservation of fetal and neonatal hematopoietic stem and progenitor cells of the blood and methods of therapeutic use |
US5004681B1 (en) * | 1987-11-12 | 2000-04-11 | Biocyte Corp | Preservation of fetal and neonatal hematopoietic stem and progenitor cells of the blood |
US5605822A (en) * | 1989-06-15 | 1997-02-25 | The Regents Of The University Of Michigan | Methods, compositions and devices for growing human hematopoietic cells |
US5464764A (en) * | 1989-08-22 | 1995-11-07 | University Of Utah Research Foundation | Positive-negative selection methods and vectors |
US5061620A (en) * | 1990-03-30 | 1991-10-29 | Systemix, Inc. | Human hematopoietic stem cell |
US5733542A (en) * | 1990-11-16 | 1998-03-31 | Haynesworth; Stephen E. | Enhancing bone marrow engraftment using MSCS |
US6010696A (en) * | 1990-11-16 | 2000-01-04 | Osiris Therapeutics, Inc. | Enhancing hematopoietic progenitor cell engraftment using mesenchymal stem cells |
US5197985A (en) * | 1990-11-16 | 1993-03-30 | Caplan Arnold I | Method for enhancing the implantation and differentiation of marrow-derived mesenchymal cells |
US5486359A (en) * | 1990-11-16 | 1996-01-23 | Osiris Therapeutics, Inc. | Human mesenchymal stem cells |
RU2155066C2 (ru) * | 1993-03-31 | 2000-08-27 | Про-Ньюрон, Инк. | Ингибитор пролиферации стволовых клеток и его использование |
US5709854A (en) * | 1993-04-30 | 1998-01-20 | Massachusetts Institute Of Technology | Tissue formation by injecting a cell-polymeric solution that gels in vivo |
US5591625A (en) * | 1993-11-24 | 1997-01-07 | Case Western Reserve University | Transduced mesenchymal stem cells |
US6288030B1 (en) * | 1993-12-22 | 2001-09-11 | Amgen Inc. | Stem cell factor formulations and methods |
DE69531638T2 (de) * | 1994-06-06 | 2004-06-17 | Osiris Therapeutics, Inc. | Biomatrix für geweberegenaration |
US6174333B1 (en) * | 1994-06-06 | 2001-01-16 | Osiris Therapeutics, Inc. | Biomatrix for soft tissue regeneration using mesenchymal stem cells |
US6103522A (en) * | 1994-07-20 | 2000-08-15 | Fred Hutchinson Cancer Research Center | Human marrow stromal cell lines which sustain hematopoiesis |
US5874301A (en) * | 1994-11-21 | 1999-02-23 | National Jewish Center For Immunology And Respiratory Medicine | Embryonic cell populations and methods to isolate such populations |
US5736396A (en) * | 1995-01-24 | 1998-04-07 | Case Western Reserve University | Lineage-directed induction of human mesenchymal stem cell differentiation |
US5695998A (en) * | 1995-02-10 | 1997-12-09 | Purdue Research Foundation | Submucosa as a growth substrate for islet cells |
US6011000A (en) * | 1995-03-03 | 2000-01-04 | Perrine; Susan P. | Compositions for the treatment of blood disorders |
US5716616A (en) * | 1995-03-28 | 1998-02-10 | Thomas Jefferson University | Isolated stromal cells for treating diseases, disorders or conditions characterized by bone defects |
US5733541A (en) * | 1995-04-21 | 1998-03-31 | The Regent Of The University Of Michigan | Hematopoietic cells: compositions and methods |
US5925567A (en) * | 1995-05-19 | 1999-07-20 | T. Breeders, Inc. | Selective expansion of target cell populations |
US5877299A (en) * | 1995-06-16 | 1999-03-02 | Stemcell Technologies Inc. | Methods for preparing enriched human hematopoietic cell preparations |
US5858782A (en) * | 1995-11-13 | 1999-01-12 | Regents Of The University Of Michigan | Functional human hematopoietic cells |
WO1997019172A1 (fr) * | 1995-11-17 | 1997-05-29 | Asahi Kasei Kogyo Kabushiki Kaisha | Polypeptide suppresseur et de differenciation |
US5716794A (en) * | 1996-03-29 | 1998-02-10 | Xybernaut Corporation | Celiac antigen |
CA2251983C (en) * | 1996-04-19 | 2003-12-16 | Sudhakar Kadiyala | Regeneration and augmentation of bone using mesenchymal stem cells |
US5919176A (en) * | 1996-05-14 | 1999-07-06 | Children's Hospital Medical Center Of Northern California | Apparatus and method for collecting blood from an umbilical cord |
US5827740A (en) * | 1996-07-30 | 1998-10-27 | Osiris Therapeutics, Inc. | Adipogenic differentiation of human mesenchymal stem cells |
US5916202A (en) * | 1996-08-30 | 1999-06-29 | Haswell; John N. | Umbilical cord blood collection |
US6335195B1 (en) * | 1997-01-28 | 2002-01-01 | Maret Corporation | Method for promoting hematopoietic and mesenchymal cell proliferation and differentiation |
US5879318A (en) * | 1997-08-18 | 1999-03-09 | Npbi International B.V. | Method of and closed system for collecting and processing umbilical cord blood |
WO1999011287A1 (en) * | 1997-09-04 | 1999-03-11 | Osiris Therapeutics, Inc. | Ligands that modulate differentiation of mesenchymal stem cells |
WO1999046366A1 (en) * | 1998-03-13 | 1999-09-16 | Osiris Therapeutics, Inc. | Uses for humane non-autologous mesenchymal stem cells |
JP4526186B2 (ja) * | 1998-06-08 | 2010-08-18 | オシリス セラピューティクス,インコーポレイテッド | 造血幹細胞を試験管内で維持する方法と組成物 |
US6184035B1 (en) * | 1998-11-18 | 2001-02-06 | California Institute Of Technology | Methods for isolation and activation of, and control of differentiation from, skeletal muscle stem or progenitor cells |
JP3089299B2 (ja) * | 1998-12-14 | 2000-09-18 | 京都大学長 | 生体内に毛細血管が豊富な組織を作成するのに用いる新生血管床形成用用具 |
RU2249039C2 (ru) * | 1999-02-04 | 2005-03-27 | Текнион Рисерч Энд Дивелопмент Фаундейшн Лтд. | Способ размножения/поддержания недифференцированных гемопоэтических стволовых клеток или клеток-предшественников (варианты), способ приготовления кондиционированной среды стромальных клеток, способ трансплантации недифференцированных гемопоэтических стволовых клеток или клеток-предшественников (варианты) |
FR2792202B1 (fr) * | 1999-04-19 | 2003-06-13 | Pharmascience Lab | Extrait peptidique de lupin et composition pharmaceutique ou cosmetique ou nutraceutique comprenant un tel extrait |
US8075881B2 (en) * | 1999-08-05 | 2011-12-13 | Regents Of The University Of Minnesota | Use of multipotent adult stem cells in treatment of myocardial infarction and congestive heart failure |
US6685936B2 (en) * | 1999-10-12 | 2004-02-03 | Osiris Therapeutics, Inc. | Suppressor cells induced by culture with mesenchymal stem cells for treatment of immune responses in transplantation |
US20050009876A1 (en) * | 2000-07-31 | 2005-01-13 | Bhagwat Shripad S. | Indazole compounds, compositions thereof and methods of treatment therewith |
CA2678490A1 (en) * | 2000-12-06 | 2002-06-13 | Robert J. Hariri | Isolated placental perfusate and placental cells isolated therefrom |
US7311905B2 (en) * | 2002-02-13 | 2007-12-25 | Anthrogenesis Corporation | Embryonic-like stem cells derived from post-partum mammalian placenta, and uses and methods of treatment using said cells |
US20030045552A1 (en) * | 2000-12-27 | 2003-03-06 | Robarge Michael J. | Isoindole-imide compounds, compositions, and uses thereof |
KR101132545B1 (ko) * | 2001-02-14 | 2012-04-02 | 안트로제네시스 코포레이션 | 산후 포유류의 태반, 이의 용도 및 태반 줄기세포 |
JP2004528021A (ja) * | 2001-02-14 | 2004-09-16 | アンスロジェネシス コーポレーション | 分娩後の哺乳動物の胎盤、その使用およびそれに由来する胎盤幹細胞 |
US20030044977A1 (en) * | 2001-08-10 | 2003-03-06 | Norio Sakuragawa | Human stem cells originated from human amniotic mesenchymal cell layer |
AU2003205266A1 (en) * | 2002-01-22 | 2003-09-02 | Advanced Cell Technology, Inc. | Stem cell-derived endothelial cells modified to disrupt tumor angiogenesis |
NZ534643A (en) * | 2002-02-13 | 2010-06-25 | Anthrogenesis Corp | Embryonic-like stem cells derived from post-partum mammalian placenta and uses and methods of treatment using said cells |
GB0205867D0 (en) * | 2002-03-13 | 2002-04-24 | Univ Nottingham | Polymer composite loaded with functioning matter |
US20030187515A1 (en) * | 2002-03-26 | 2003-10-02 | Hariri Robert J. | Collagen biofabric and methods of preparing and using the collagen biofabric |
US7498171B2 (en) * | 2002-04-12 | 2009-03-03 | Anthrogenesis Corporation | Modulation of stem and progenitor cell differentiation, assays, and uses thereof |
JP2005528105A (ja) * | 2002-05-30 | 2005-09-22 | セルジーン・コーポレーション | 細胞分化をモジュレートするため、並びに骨髄増殖性疾患及び骨髄異形成症候群を治療するためのjnk又はmkk阻害剤の使用方法 |
US7422736B2 (en) * | 2002-07-26 | 2008-09-09 | Food Industry Research And Development Institute | Somatic pluripotent cells |
JP4480128B2 (ja) * | 2002-11-20 | 2010-06-16 | 独立行政法人科学技術振興機構 | マトリックスメタロプロテアーゼ−9の産生を阻害するための薬剤 |
BRPI0407427A (pt) * | 2003-02-13 | 2006-01-24 | Anthrogenesis Corp | Método para tratar um paciente e para tratar a mielodisplasia |
PL1649013T3 (pl) * | 2003-06-27 | 2016-07-29 | Depuy Synthes Products Inc | Regeneracja i naprawa chrząstki i kości z wykorzystaniem komórek poporodowych |
US7569385B2 (en) * | 2003-08-14 | 2009-08-04 | The Regents Of The University Of California | Multipotent amniotic fetal stem cells |
US20080044392A1 (en) * | 2003-10-17 | 2008-02-21 | Innovative Dairy Products Pty Ltd As Trustee For The Participants Of The Coooperative Research Ctr | Isolation of Stem Cell-Like Cells and Use Thereof |
WO2005063807A2 (en) * | 2003-12-29 | 2005-07-14 | Centelion | Treatment of coronary or peripheral ischemia |
BRPI0510271A (pt) * | 2004-06-15 | 2007-10-30 | Baxter Int | aplicações ex-vivo agentes terapêuticos microparticulados |
US7909806B2 (en) * | 2004-09-23 | 2011-03-22 | Anthrogenesis Corporation | Cord blood and placenta collection kit |
US7147626B2 (en) * | 2004-09-23 | 2006-12-12 | Celgene Corporation | Cord blood and placenta collection kit |
US8017395B2 (en) * | 2004-12-17 | 2011-09-13 | Lifescan, Inc. | Seeding cells on porous supports |
US9056093B2 (en) * | 2005-01-07 | 2015-06-16 | Wake Forest University Health Sciences | Regeneration of pancreatic islets by amniotic fluid stem cell therapy |
WO2006091766A2 (en) * | 2005-02-24 | 2006-08-31 | Jau-Nan Lee | Human trophoblast stem cells and use thereof |
US20060222634A1 (en) * | 2005-03-31 | 2006-10-05 | Clarke Diana L | Amnion-derived cell compositions, methods of making and uses thereof |
EP1869165B1 (en) * | 2005-04-12 | 2015-10-21 | Mesoblast, Inc. | Isolation of adult multipotential cells by tissue non-specific alkaline phosphatase |
NZ564563A (en) * | 2005-06-10 | 2011-03-31 | Celgene Corp | Human placental collagen compositions, processes for their preparation, methods of their use and kits comprising the compositions |
MX2007016268A (es) * | 2005-06-30 | 2009-02-23 | Anthrogenesis Corp | Reparacion de membrana timpanica utilizando biotela de colageno derivado de placenta. |
WO2007009062A2 (en) * | 2005-07-13 | 2007-01-18 | Anthrogenesis Corporation | Treatment of leg ulcers using placenta derived collagen biofabric |
EP1919365A2 (en) * | 2005-07-13 | 2008-05-14 | Anthrogenesis Corporation | Ocular plug formed from placenta derived collagen biofabric |
WO2007011693A2 (en) * | 2005-07-14 | 2007-01-25 | Medistem Laboratories, Inc. | Compositions of placentally-derived stem cells for the treatment of cancer |
PE20070771A1 (es) * | 2005-10-13 | 2007-08-11 | Anthrogenesis Corp | Inmunomodulacion mediante el uso de celulas madres de la placenta |
ES2628129T3 (es) * | 2005-12-28 | 2017-08-01 | DePuy Synthes Products, Inc. | Tratamiento de la enfermedad vascular periférica utilizando células derivadas del posparto |
ES2708933T3 (es) * | 2005-12-29 | 2019-04-12 | Celularity Inc | Poblaciones de células madre placentarias |
US20080050814A1 (en) * | 2006-06-05 | 2008-02-28 | Cryo-Cell International, Inc. | Procurement, isolation and cryopreservation of fetal placental cells |
WO2007146105A2 (en) * | 2006-06-05 | 2007-12-21 | Cryo-Cell International, Inc. | Procurement, isolation and cryopreservation of fetal placental cells |
AU2007258514A1 (en) * | 2006-06-09 | 2007-12-21 | Anthrogenesis Corporation | Placental niche and use thereof to culture stem cells |
US20090081171A1 (en) * | 2006-08-11 | 2009-03-26 | Yu-Show Fu | Cell system for alleviating syndromes of Parkinson's disease in a mammal |
US8105634B2 (en) * | 2006-08-15 | 2012-01-31 | Anthrogenesis Corporation | Umbilical cord biomaterial for medical use |
US20080050347A1 (en) * | 2006-08-23 | 2008-02-28 | Ichim Thomas E | Stem cell therapy for cardiac valvular dysfunction |
PT2084268T (pt) * | 2006-10-23 | 2019-01-28 | Celularity Inc | Métodos e composições para o tratamento de defeitos ósseos com populações de células placentárias |
EP2129775A1 (en) * | 2007-02-12 | 2009-12-09 | Anthrogenesis Corporation | Hepatocytes and chondrocytes from adherent placental stem cells; and cd34+, cd45- placental stem cell-enriched cell populations |
WO2008148105A1 (en) * | 2007-05-25 | 2008-12-04 | Medistem Laboratories, Inc. | Endometrial stem cells and methods of making and using same |
US20090016999A1 (en) * | 2007-07-13 | 2009-01-15 | Michael Cohen | Embryonic cell compositions for wound treatment |
CA2630708C (en) * | 2007-09-13 | 2017-08-01 | Clifford L. Librach | Method of isolation and use of cells derived from first trimester umbilical cord tissue |
PL2200622T5 (pl) * | 2007-09-19 | 2016-08-31 | Pluristem Ltd | Adherentne komórki z tkanki tłuszczowej i łożyska i ich zastosowanie w terapii |
KR20190050867A (ko) * | 2007-09-26 | 2019-05-13 | 안트로제네시스 코포레이션 | 인간 태반 관류액으로부터의 혈관형성 세포 |
EP2329012B1 (en) * | 2008-08-20 | 2020-05-20 | Celularity, Inc. | Treatment of stroke using isolated placental cells |
NZ591292A (en) * | 2008-08-20 | 2012-10-26 | Anthrogenesis Corp | Improved cell composition and methods of making the same |
CA2734446C (en) * | 2008-08-22 | 2017-06-20 | Anthrogenesis Corporation | Methods and compositions for treatment of bone defects with placental cell populations |
CN201299504Y (zh) * | 2008-11-11 | 2009-09-02 | 薛华 | 一种方便搭挂的毛巾 |
NZ597436A (en) * | 2009-07-02 | 2014-08-29 | Anthrogenesis Corp | Method of producing erythrocytes without feeder cells |
TWI395125B (zh) * | 2009-07-14 | 2013-05-01 | Sonix Technology Co Ltd | 電容式觸控感應電路 |
-
2008
- 2008-09-26 KR KR1020197012717A patent/KR20190050867A/ko not_active Application Discontinuation
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