KR920702410A - 수정된 생물학적 물질 - Google Patents

수정된 생물학적 물질

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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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hcrf
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tissue
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제임스 그라함 화이트 데이비드
프레드릭 윌리암스 알란
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원본미기재
임뮤트란 리미티드
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Priority claimed from GB898922987A external-priority patent/GB8922987D0/en
Priority claimed from GB909017198A external-priority patent/GB9017198D0/en
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Publication of KR920702410A publication Critical patent/KR920702410A/ko

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Abstract

내용 없음

Description

수정된 생물학적 물질
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)

  1. 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.
  2. 제1항에 있어서, 조직(tissue)이 장기(organ)인 방법.
  3. 제2항에 있어서, 장기(organ)가 심장, 폐, 간장, 신장, 취장및 갑상샘인 방법.
  4. 제1항에 있어서, 조직이 혈액 및 조혈세포, 랑겔한스샘, 뇌세포 및 내분비기관 (endocrime organ)의 세포인 방법.
  5. 제1항 내지 제4항중 어느 한 항에 있어서, HCRF가 고전적 보체활성화경로 및 부보체 활성화경로 모두에 공통적인 보체활성화 케스캐이드 중 어느 단계를 방해하는 방법.
  6. 제1항내지 제5항중 어느 한 항에 있어서, HCRF가 자연상의 HCRF인 방법.
  7. 제5항에 있어서, HCRF가 C3단계에서의 보체활성화를 조절하는 방법.
  8. 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.
  9. 제1항 내지 제8항중 어느 한항에 있어서 HCRF가 염색체 1의 q32위치에 염색체 지도작성되는 RCA(보체활성조절인자)부위에 유전자가 위치한 자연상의 HCRF인 방법.
  10. 제5항에 있어서 HCRF가 C3단계 및/또는 C9단계에서 보체활성을 조절하는 방법.
  11. 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.
  12. 제1항 내지 제1항중 어느 한항에 있어서 HCRF가 막에 결합되어져 있는 방법.
  13. 제1항 내지 제12항중 어느 한 항에 있어서 HCRF가 공여체조직의 세포막에 걸합되어진 상태로 제공되는 방법.
  14. 제13항에 있어서, 수용체에 이식되었을때 수용체 종에서 활성을 띠는 한개 이상의 HCRFS를 코딩하는 핵산을 가지고 있으며 이들을 발현하는 공여조직이 트란스제닉한(transgenic)방법.
  15. 제1항 내지 제14항중 어느 한항에 있어서, 수용체 종이 사람인 방법.
  16. 제1항 내지 제15항중 어느 한항에 있어서 공여종이 돼지인 방법.
  17. 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.
  18. 적어도 한가지 디스코던트한 종의 면역계에 노출되거나 또는 장기이식을 하였을 때 이종이식편 거부반응을 일으키지 않는 이식될 수 있는 조직을 가지고 있는 트란스제제닉한 동물(transgenic animal).
  19. 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.
  20. 다른종의 동종보체억제인자를 발현할 수 있는 세포를 가지는 트란스제닉한 동물.
  21. 동물세포에 대해 디스코던트한 종에서 활성화되는 한개이상의 동종보체억제인자를 발현할 수 있는 비형질전환 동물세포 (non-transformed animal cell).
  22. 적어도 한개의 동종보체억제인자를 코팅하는 DNA와 이들 코딩 DNA가 비형질전화세포에 의해 발현되어지도록 할 수 있는 한개 이상의 염기서열로 구성된 제조합 DNA.
  23. 제22항에 있어서 동물세포가 유전조작물을 유전적으로 통합된 트란스제닉한 동물의 세포인 DNA.
  24. 제22항에 있어서, 세포가 랑겔한스샘과 같은 배양된 기관 또는 다른 조직으로된 DNA.
  25. 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.
  26. 제25항에 있어서, YAC의 형태를 가지는 유전 조작물.
  27. 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.
KR1019920700843A 1989-10-12 1990-10-12 수정된 생물학적 물질 KR920702410A (ko)

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Application Number Priority Date Filing Date Title
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

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