KR920702410A - 수정된 생물학적 물질 - Google Patents
수정된 생물학적 물질Info
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- KR920702410A KR920702410A KR1019920700843A KR920700843A KR920702410A KR 920702410 A KR920702410 A KR 920702410A KR 1019920700843 A KR1019920700843 A KR 1019920700843A KR 920700843 A KR920700843 A KR 920700843A KR 920702410 A KR920702410 A KR 920702410A
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- 239000012620 biological material Substances 0.000 title 1
- 241000894007 species Species 0.000 claims 18
- 238000000034 method Methods 0.000 claims 16
- 102000005962 receptors Human genes 0.000 claims 14
- 108020003175 receptors Proteins 0.000 claims 14
- 210000001519 tissue Anatomy 0.000 claims 13
- 241001465754 Metazoa Species 0.000 claims 12
- 210000004027 cell Anatomy 0.000 claims 9
- 230000009261 transgenic effect Effects 0.000 claims 8
- 210000000056 organ Anatomy 0.000 claims 6
- 230000024203 complement activation Effects 0.000 claims 5
- 210000004102 animal cell Anatomy 0.000 claims 4
- 230000000694 effects Effects 0.000 claims 4
- 102100022002 CD59 glycoprotein Human genes 0.000 claims 3
- 102100030886 Complement receptor type 1 Human genes 0.000 claims 3
- 102100032768 Complement receptor type 2 Human genes 0.000 claims 3
- 101000897400 Homo sapiens CD59 glycoprotein Proteins 0.000 claims 3
- 101000727061 Homo sapiens Complement receptor type 1 Proteins 0.000 claims 3
- 102100039373 Membrane cofactor protein Human genes 0.000 claims 3
- 239000004074 complement inhibitor Substances 0.000 claims 3
- 230000002068 genetic effect Effects 0.000 claims 3
- 239000003112 inhibitor Substances 0.000 claims 3
- 108090000623 proteins and genes Proteins 0.000 claims 3
- 229940124073 Complement inhibitor Drugs 0.000 claims 2
- 101000941929 Homo sapiens Complement receptor type 2 Proteins 0.000 claims 2
- 210000000349 chromosome Anatomy 0.000 claims 2
- 230000000295 complement effect Effects 0.000 claims 2
- 238000010353 genetic engineering Methods 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 238000002054 transplantation Methods 0.000 claims 2
- 102000016550 Complement Factor H Human genes 0.000 claims 1
- 108010053085 Complement Factor H Proteins 0.000 claims 1
- 102000003689 Complement Factor I Human genes 0.000 claims 1
- 108090000044 Complement Factor I Proteins 0.000 claims 1
- 102100025680 Complement decay-accelerating factor Human genes 0.000 claims 1
- 102100035431 Complement factor I Human genes 0.000 claims 1
- 101000856022 Homo sapiens Complement decay-accelerating factor Proteins 0.000 claims 1
- 101000961414 Homo sapiens Membrane cofactor protein Proteins 0.000 claims 1
- 101710146216 Membrane cofactor protein Proteins 0.000 claims 1
- 102000023732 binding proteins Human genes 0.000 claims 1
- 108091008324 binding proteins Proteins 0.000 claims 1
- 239000008280 blood Substances 0.000 claims 1
- 210000000601 blood cell Anatomy 0.000 claims 1
- 210000004958 brain cell Anatomy 0.000 claims 1
- 210000000170 cell membrane Anatomy 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 210000001072 colon Anatomy 0.000 claims 1
- 230000002124 endocrine Effects 0.000 claims 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 claims 1
- 210000004907 gland Anatomy 0.000 claims 1
- 210000002216 heart Anatomy 0.000 claims 1
- 210000003958 hematopoietic stem cell Anatomy 0.000 claims 1
- 210000000987 immune system Anatomy 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 230000010354 integration Effects 0.000 claims 1
- 210000003734 kidney Anatomy 0.000 claims 1
- 210000004185 liver Anatomy 0.000 claims 1
- 210000004072 lung Anatomy 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- 102000039446 nucleic acids Human genes 0.000 claims 1
- 108020004707 nucleic acids Proteins 0.000 claims 1
- 150000007523 nucleic acids Chemical class 0.000 claims 1
- 230000037361 pathway Effects 0.000 claims 1
- 210000001685 thyroid gland Anatomy 0.000 claims 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000006037 cell lysis Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000003127 radioimmunoassay Methods 0.000 description 1
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- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
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- A01K2217/00—Genetically modified animals
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제2도는 실시예 1에서 사용된 돼지들이 항종항체(antispecies antibody)를 가지고 있지 않다는 것을 나타내는 방사면역분석(radioimmunoassay)의 결과이다 ; 제6도는 실시예 5에서 사용한 크롬 방출세포용해분석법(chromium release cell lysis assay)의 결과를 나타낸다.
Claims (27)
- 수용체와 다른 종으로서, 수용체와 불일치하는(discordant)종인 공여체로부터 얻어진 동물조직을 수용체에 이식하고, 보체의 완전활성을 방지하기 위해 수용체종에 한개이상의 동종보체억제인자(HCRFS)를 이식장기와 연관하여 제공하는 것으로 구성된 동물조직을 수용체에 장기이식하는 방법.
- 제1항에 있어서, 조직(tissue)이 장기(organ)인 방법.
- 제2항에 있어서, 장기(organ)가 심장, 폐, 간장, 신장, 취장및 갑상샘인 방법.
- 제1항에 있어서, 조직이 혈액 및 조혈세포, 랑겔한스샘, 뇌세포 및 내분비기관 (endocrime organ)의 세포인 방법.
- 제1항 내지 제4항중 어느 한 항에 있어서, HCRF가 고전적 보체활성화경로 및 부보체 활성화경로 모두에 공통적인 보체활성화 케스캐이드 중 어느 단계를 방해하는 방법.
- 제1항내지 제5항중 어느 한 항에 있어서, HCRF가 자연상의 HCRF인 방법.
- 제5항에 있어서, HCRF가 C3단계에서의 보체활성화를 조절하는 방법.
- 제7항에 있어서, HCRF가 I인자 (이미 C3b 불활성화제 또는 KAF로 알려져있음); H인자;C4 결합 단백질; DAF(CD55로서 알려져 있음);막보조인자 단백질(MCP;또한 CD46으로써 알려져 있으며 처음에는 gp45-70으로서 설명되었고 gp66/56으로서 더 많이 알려져 있음) CR1(C3b/C4b 리셉터 또는 CD35로서 알려져 있음); 및/ 또한 CR2(CD21, C3,dg 리셉터, 3d/EBV 리셉터 및 P140)이거나 이들의 활성을 가지는 방법.
- 제1항 내지 제8항중 어느 한항에 있어서 HCRF가 염색체 1의 q32위치에 염색체 지도작성되는 RCA(보체활성조절인자)부위에 유전자가 위치한 자연상의 HCRF인 방법.
- 제5항에 있어서 HCRF가 C3단계 및/또는 C9단계에서 보체활성을 조절하는 방법.
- 제10항에 있어서 HCRF가 C3bp (또한 HRF 또는 MIP로서 알려져 있음);P-18(또한 HRF -20, CD59 또는 MIRL로서 알려져 있음)또는 SP40.40이거나 이들의 활성을 가지고 있는 방법.
- 제1항 내지 제1항중 어느 한항에 있어서 HCRF가 막에 결합되어져 있는 방법.
- 제1항 내지 제12항중 어느 한 항에 있어서 HCRF가 공여체조직의 세포막에 걸합되어진 상태로 제공되는 방법.
- 제13항에 있어서, 수용체에 이식되었을때 수용체 종에서 활성을 띠는 한개 이상의 HCRFS를 코딩하는 핵산을 가지고 있으며 이들을 발현하는 공여조직이 트란스제닉한(transgenic)방법.
- 제1항 내지 제14항중 어느 한항에 있어서, 수용체 종이 사람인 방법.
- 제1항 내지 제15항중 어느 한항에 있어서 공여종이 돼지인 방법.
- 세포 또는 조직은 보체의 완전활성을 방지하기위해 수용체 종에서 활성을 띠는 한개이상의 동종 보체억제인자를 가지고 있고 공여체종은 수용체에 대하여 디스코던트한 종인 공여체종의 이식될 수 있는 동물세포 또는 조직.
- 적어도 한가지 디스코던트한 종의 면역계에 노출되거나 또는 장기이식을 하였을 때 이종이식편 거부반응을 일으키지 않는 이식될 수 있는 조직을 가지고 있는 트란스제제닉한 동물(transgenic animal).
- 수용체종으로 이식될 수 있는 조직을 제조함에 있어서 공여체종이 수용체종에 대하여 디스코던트한 종인 공여체종으로 부터 얻어진 동물조직 및 수용체 종에서 활성을 띄는 하나이상의 동종보체 억제인자의 사용.
- 다른종의 동종보체억제인자를 발현할 수 있는 세포를 가지는 트란스제닉한 동물.
- 동물세포에 대해 디스코던트한 종에서 활성화되는 한개이상의 동종보체억제인자를 발현할 수 있는 비형질전환 동물세포 (non-transformed animal cell).
- 적어도 한개의 동종보체억제인자를 코팅하는 DNA와 이들 코딩 DNA가 비형질전화세포에 의해 발현되어지도록 할 수 있는 한개 이상의 염기서열로 구성된 제조합 DNA.
- 제22항에 있어서 동물세포가 유전조작물을 유전적으로 통합된 트란스제닉한 동물의 세포인 DNA.
- 제22항에 있어서, 세포가 랑겔한스샘과 같은 배양된 기관 또는 다른 조직으로된 DNA.
- 적어도 한개의 동종 보체억제인자를 코딩하는 DNA와 유전조작물이 유전적으로 통합된 트란스제닉한 동물의 적어도 어떤 세포에서 그 코딩 DNA가 발현될 수 있도록 하는 한개 이상의 염기서열로 구성된 유전조작물로서의 트란스제닉한 동물을 만들기위해 동물의 유전물질로 통합되기에 적합한 유전조작물.
- 제25항에 있어서, YAC의 형태를 가지는 유전 조작물.
- 적어도 한개의 동종보체억제인자를 코딩하는 DNA와 코딩 DNA가 트란스제닉한 동물의 적어도 어떤 세포에서 발혈될수 있도록 하는 한개 이상의 염기서열을 가지는 DNA를 동물의 유전물질로 통합시키는 것으로 구성된 트란스제닉한 동물의 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (5)
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---|---|---|---|
GB898922987A GB8922987D0 (en) | 1989-10-12 | 1989-10-12 | Modified biological material |
GB89229878 | 1989-10-12 | ||
GB909017198A GB9017198D0 (en) | 1990-08-06 | 1990-08-06 | Modified biological material |
GB90171984 | 1990-08-06 | ||
PCT/GB1990/001575 WO1991005855A1 (en) | 1989-10-12 | 1990-10-12 | Modified biological material |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019997005897A Division KR100317106B1 (ko) | 1989-10-12 | 1990-10-12 | 수정된 생물학적 물질 |
Publications (1)
Publication Number | Publication Date |
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KR920702410A true KR920702410A (ko) | 1992-09-04 |
Family
ID=26296038
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019920700843A KR920702410A (ko) | 1989-10-12 | 1990-10-12 | 수정된 생물학적 물질 |
KR1019997005897A KR100317106B1 (ko) | 1989-10-12 | 1990-10-12 | 수정된 생물학적 물질 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019997005897A KR100317106B1 (ko) | 1989-10-12 | 1990-10-12 | 수정된 생물학적 물질 |
Country Status (27)
Country | Link |
---|---|
US (1) | US6495735B1 (ko) |
EP (2) | EP0709459A3 (ko) |
JP (1) | JP3302358B2 (ko) |
KR (2) | KR920702410A (ko) |
CN (2) | CN1122719C (ko) |
AT (1) | ATE139562T1 (ko) |
AU (1) | AU654116B2 (ko) |
BG (1) | BG61080B1 (ko) |
CA (1) | CA2067235A1 (ko) |
CY (1) | CY1996A (ko) |
DE (2) | DE69027535T2 (ko) |
DK (1) | DK0495852T3 (ko) |
ES (1) | ES2060561T3 (ko) |
FI (1) | FI921618A0 (ko) |
GR (2) | GR940300004T1 (ko) |
HK (1) | HK48497A (ko) |
HU (1) | HUT64584A (ko) |
IE (1) | IE75345B1 (ko) |
IL (2) | IL95970A0 (ko) |
IN (1) | IN171948B (ko) |
MY (1) | MY107433A (ko) |
NO (2) | NO303502B1 (ko) |
NZ (2) | NZ235657A (ko) |
PT (2) | PT95580B (ko) |
RO (1) | RO109863B1 (ko) |
SG (1) | SG72614A1 (ko) |
WO (1) | WO1991005855A1 (ko) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
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US5705732A (en) * | 1989-06-12 | 1998-01-06 | Oklahoma Medical Research Foundation | Universal donor cells |
JP2750220B2 (ja) * | 1989-07-21 | 1998-05-13 | ワシントン ユニバーシティ | 組換え産生したヒト細胞膜補助因子タンパク(mcp) |
DE69133111D1 (de) * | 1990-05-11 | 2002-10-24 | Austin Res Inst Heidelberg | CD46 Isoformen |
US5846715A (en) * | 1990-05-11 | 1998-12-08 | The Austin Research Institute | CD46 variants |
JPH06506604A (ja) * | 1991-07-15 | 1994-07-28 | オクラホマ メディカル リサーチ ファウンデーション | 自在なドナー細胞 |
US6916654B1 (en) * | 1992-06-29 | 2005-07-12 | Oklahoma Medical Research Foundation | Universal donor cells |
EP0662125A1 (en) * | 1992-09-22 | 1995-07-12 | Dnx Biotherapeutics, Inc. | Delivery of proteins by intermembrane transfer for preaccommodation of xenogeneic organ transplants and other purposes |
US5627264A (en) * | 1994-03-03 | 1997-05-06 | Alexion Pharmaceuticals, Inc. | Chimeric complement inhibitor proteins |
CA2196311A1 (en) * | 1994-08-19 | 1996-02-29 | David H. Sachs | Genetically engineered swine cells |
CA2227584A1 (en) | 1995-08-04 | 1997-02-20 | The General Hospital Corporation | Transgenic swine and swine cells having human hla genes |
US6166288A (en) * | 1995-09-27 | 2000-12-26 | Nextran Inc. | Method of producing transgenic animals for xenotransplantation expressing both an enzyme masking or reducing the level of the gal epitope and a complement inhibitor |
WO1997035886A1 (en) * | 1996-03-22 | 1997-10-02 | Imutran Limited | Surfaces which prevent or reduce complement activation |
DE69833545T2 (de) | 1997-03-26 | 2006-12-14 | Imperial College Innovations Ltd. | In der zellmembran verankertes antikoagulant-fusionsprotein |
ATE313256T1 (de) | 1997-07-14 | 2006-01-15 | Nippon Meat Packers | Transgene schweine |
US7419683B2 (en) * | 1997-10-31 | 2008-09-02 | United States Of America As Represented By The Secretary Of The Army | Method of inhibiting side effects of pharmaceutical compositions containing amphiphilic vehicles or drug carrier molecules |
SE523817C2 (sv) * | 1999-02-05 | 2004-05-18 | Corline Systems Ab | Användning av ett koagulationsförebyggande ämne i samband med transplantation av insulinproducerande celler |
GB9905503D0 (en) | 1999-03-10 | 1999-05-05 | Adprotech Plc | Novel compound formulations and methods of delivery |
EP1651050B1 (en) * | 2003-07-21 | 2012-08-22 | Lifecell Corporation | Acellular tissue matrices made from galactose alpha-1,3-galactose -deficient tissue |
CA3104704A1 (en) | 2009-08-14 | 2011-02-17 | Revivicor, Inc. | Multi-transgenic pigs for diabetes treatment |
US9420770B2 (en) | 2009-12-01 | 2016-08-23 | Indiana University Research & Technology Corporation | Methods of modulating thrombocytopenia and modified transgenic pigs |
CN106620693A (zh) | 2010-09-03 | 2017-05-10 | 艾伯维施特姆森特克斯有限责任公司 | 新型调节剂及使用方法 |
EP2675901B1 (en) | 2011-02-14 | 2018-05-30 | Revivicor, Inc. | Genetically modified pigs for xenotransplantation of vascularized xenografts and derivatives thereof |
AU2014341866B2 (en) | 2013-11-04 | 2018-07-05 | Lifecell Corporation | Methods of removing alpha-galactose |
CN114686427B (zh) * | 2022-05-23 | 2022-07-29 | 中国人民解放军总医院第一医学中心 | 一种脾脏调节型b淋巴细胞及其制备方法与应用 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
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WO1982004443A1 (en) * | 1981-06-12 | 1982-12-23 | Ohio Univ | Genetic transformation of zygotes |
US4431636A (en) | 1982-05-24 | 1984-02-14 | American Cyanamid Company | Bis(4-O-polyhexaose-thio)-phenyl ureas and method of use |
US5109113A (en) * | 1986-05-02 | 1992-04-28 | Genentech, Inc. | Membrane anchor fusion polypeptides |
JPS62104594A (ja) * | 1985-10-31 | 1987-05-15 | Terumo Corp | クエン酸塩利用能検査用培地組成物 |
JPH0742235B2 (ja) * | 1985-11-08 | 1995-05-10 | 三共株式会社 | 自己免疫性疾病の予防・治療剤 |
IL82390A0 (en) * | 1986-05-02 | 1987-10-30 | Genentech Inc | Nucleic acid and methods for the synthesis of novel daf compositions |
GB8615942D0 (en) * | 1986-06-30 | 1986-08-06 | Animal & Food Research Council | Peptide production |
IL89790A (en) * | 1988-04-01 | 2002-05-23 | Johns Hopking University | Sequences of nucleic acids encoding and cells producing CR1 protein and methods for its production and purification |
DE3830271A1 (de) | 1988-09-06 | 1990-03-15 | Goetze Otto | Mittel mit immunsuppressiver wirkung |
US5573940A (en) * | 1989-06-12 | 1996-11-12 | Oklahoma Medical Research Foundation | Cells expressing high levels of CD59 |
-
1990
- 1990-10-12 HU HU9201240A patent/HUT64584A/hu unknown
- 1990-10-12 KR KR1019920700843A patent/KR920702410A/ko not_active Application Discontinuation
- 1990-10-12 ES ES90915320T patent/ES2060561T3/es not_active Expired - Lifetime
- 1990-10-12 CA CA002067235A patent/CA2067235A1/en not_active Abandoned
- 1990-10-12 PT PT95580A patent/PT95580B/pt not_active IP Right Cessation
- 1990-10-12 RO RO92-200502A patent/RO109863B1/ro unknown
- 1990-10-12 DE DE69027535T patent/DE69027535T2/de not_active Expired - Fee Related
- 1990-10-12 SG SG1996001903A patent/SG72614A1/en unknown
- 1990-10-12 MY MYPI90001781A patent/MY107433A/en unknown
- 1990-10-12 DK DK90915320.7T patent/DK0495852T3/da active
- 1990-10-12 CN CN90108275A patent/CN1122719C/zh not_active Expired - Fee Related
- 1990-10-12 NZ NZ235657A patent/NZ235657A/en unknown
- 1990-10-12 AT AT90915320T patent/ATE139562T1/de not_active IP Right Cessation
- 1990-10-12 JP JP51427990A patent/JP3302358B2/ja not_active Ceased
- 1990-10-12 IE IE364990A patent/IE75345B1/en not_active IP Right Cessation
- 1990-10-12 IN IN872/CAL/90A patent/IN171948B/en unknown
- 1990-10-12 EP EP95118520A patent/EP0709459A3/en not_active Withdrawn
- 1990-10-12 CN CNA021302499A patent/CN1491624A/zh active Pending
- 1990-10-12 NZ NZ248153A patent/NZ248153A/en unknown
- 1990-10-12 KR KR1019997005897A patent/KR100317106B1/ko not_active IP Right Cessation
- 1990-10-12 EP EP90915320A patent/EP0495852B1/en not_active Expired - Lifetime
- 1990-10-12 DE DE90915320T patent/DE495852T1/de active Pending
- 1990-10-12 AU AU65392/90A patent/AU654116B2/en not_active Ceased
- 1990-10-12 WO PCT/GB1990/001575 patent/WO1991005855A1/en active Application Filing
- 1990-10-12 IL IL95970A patent/IL95970A0/xx unknown
-
1992
- 1992-04-10 NO NO921438A patent/NO303502B1/no active IP Right Review Request
- 1992-04-10 FI FI921618A patent/FI921618A0/fi not_active Application Discontinuation
- 1992-05-12 BG BG96329A patent/BG61080B1/bg unknown
-
1994
- 1994-02-28 GR GR940300004T patent/GR940300004T1/el unknown
- 1994-11-21 US US08/347,210 patent/US6495735B1/en not_active Expired - Lifetime
-
1996
- 1996-07-15 PT PT101896A patent/PT101896B/pt not_active IP Right Cessation
- 1996-08-07 GR GR960402106T patent/GR3020741T3/el unknown
-
1997
- 1997-04-17 HK HK48497A patent/HK48497A/xx not_active IP Right Cessation
- 1997-05-07 IL IL12079597A patent/IL120795A0/xx unknown
- 1997-09-05 CY CY199697A patent/CY1996A/xx unknown
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1998
- 1998-05-11 NO NO982131A patent/NO982131D0/no unknown
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