KR960701214A - 항-hiv 모노클론 항체(anti-hiv monoclonal antibody) - Google Patents
항-hiv 모노클론 항체(anti-hiv monoclonal antibody) Download PDFInfo
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- KR960701214A KR960701214A KR1019950703809A KR19950703809A KR960701214A KR 960701214 A KR960701214 A KR 960701214A KR 1019950703809 A KR1019950703809 A KR 1019950703809A KR 19950703809 A KR19950703809 A KR 19950703809A KR 960701214 A KR960701214 A KR 960701214A
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- 230000036436 anti-hiv Effects 0.000 title claims abstract 19
- 230000003472 neutralizing effect Effects 0.000 claims abstract description 7
- 239000012634 fragment Substances 0.000 claims abstract 9
- 108010047041 Complementarity Determining Regions Proteins 0.000 claims abstract 7
- 102000003886 Glycoproteins Human genes 0.000 claims abstract 5
- 108090000288 Glycoproteins Proteins 0.000 claims abstract 5
- 239000000427 antigen Substances 0.000 claims abstract 5
- 108091007433 antigens Proteins 0.000 claims abstract 5
- 102000036639 antigens Human genes 0.000 claims abstract 5
- 238000006386 neutralization reaction Methods 0.000 claims abstract 5
- 108090000765 processed proteins & peptides Proteins 0.000 claims abstract 3
- 150000001413 amino acids Chemical group 0.000 claims 24
- 241000725303 Human immunodeficiency virus Species 0.000 claims 15
- HPBNLFLSSQDFQW-WHFBIAKZSA-N Asn-Ser-Gly Chemical compound NC(=O)C[C@H](N)C(=O)N[C@@H](CO)C(=O)NCC(O)=O HPBNLFLSSQDFQW-WHFBIAKZSA-N 0.000 claims 2
- XHTUGJCAEYOZOR-UBHSHLNASA-N Asn-Ser-Trp Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O XHTUGJCAEYOZOR-UBHSHLNASA-N 0.000 claims 2
- RTXQQDVBACBSCW-CFMVVWHZSA-N Asp-Ile-Tyr Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O RTXQQDVBACBSCW-CFMVVWHZSA-N 0.000 claims 2
- BHPQOIPBLYJNAW-NGZCFLSTSA-N Gly-Ile-Pro Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)CN BHPQOIPBLYJNAW-NGZCFLSTSA-N 0.000 claims 2
- UIQGJYUEQDOODF-KWQFWETISA-N Gly-Tyr-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)CN)CC1=CC=C(O)C=C1 UIQGJYUEQDOODF-KWQFWETISA-N 0.000 claims 2
- PXHCFKXNSBJSTQ-KKUMJFAQSA-N Lys-Asn-Tyr Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCCCN)N)O PXHCFKXNSBJSTQ-KKUMJFAQSA-N 0.000 claims 2
- DIBZLYZXTSVGLN-CIUDSAMLSA-N Lys-Ser-Ser Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O DIBZLYZXTSVGLN-CIUDSAMLSA-N 0.000 claims 2
- VMLONWHIORGALA-SRVKXCTJSA-N Ser-Leu-Leu Chemical compound CC(C)C[C@@H](C([O-])=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]([NH3+])CO VMLONWHIORGALA-SRVKXCTJSA-N 0.000 claims 2
- AQAMPXBRJJWPNI-JHEQGTHGSA-N Thr-Gly-Glu Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(O)=O AQAMPXBRJJWPNI-JHEQGTHGSA-N 0.000 claims 2
- AVYVKJMBNLPWRX-WFBYXXMGSA-N Trp-Ala-Ser Chemical compound C1=CC=C2C(C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(O)=O)=CNC2=C1 AVYVKJMBNLPWRX-WFBYXXMGSA-N 0.000 claims 2
- 108010068265 aspartyltyrosine Proteins 0.000 claims 2
- 239000013604 expression vector Substances 0.000 claims 2
- XKUKSGPZAADMRA-UHFFFAOYSA-N glycyl-glycyl-glycine Chemical compound NCC(=O)NCC(=O)NCC(O)=O XKUKSGPZAADMRA-UHFFFAOYSA-N 0.000 claims 2
- 108010047748 hemorphin 4 Proteins 0.000 claims 2
- 230000003053 immunization Effects 0.000 claims 2
- 238000002649 immunization Methods 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 108010020755 prolyl-glycyl-glycine Proteins 0.000 claims 2
- 108010029020 prolylglycine Proteins 0.000 claims 2
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims 1
- PAXHINASXXXILC-SRVKXCTJSA-N Asn-Asp-Tyr Chemical compound C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(=O)N)N)O PAXHINASXXXILC-SRVKXCTJSA-N 0.000 claims 1
- MSBDSTRUMZFSEU-PEFMBERDSA-N Asn-Glu-Ile Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O MSBDSTRUMZFSEU-PEFMBERDSA-N 0.000 claims 1
- CZIVKMOEXPILDK-SRVKXCTJSA-N Asp-Tyr-Ser Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CO)C(O)=O CZIVKMOEXPILDK-SRVKXCTJSA-N 0.000 claims 1
- YIWFXZNIBQBFHR-LURJTMIESA-N Gly-His Chemical compound [NH3+]CC(=O)N[C@H](C([O-])=O)CC1=CN=CN1 YIWFXZNIBQBFHR-LURJTMIESA-N 0.000 claims 1
- WEGGKZQIJMQCGR-RECQUVTISA-N Hemorphin-4 Chemical compound C([C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H]([C@H](O)C)C(O)=O)C1=CC=C(O)C=C1 WEGGKZQIJMQCGR-RECQUVTISA-N 0.000 claims 1
- 101000597785 Homo sapiens Tumor necrosis factor receptor superfamily member 6B Proteins 0.000 claims 1
- LRAUKBMYHHNADU-DKIMLUQUSA-N Ile-Phe-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)[C@@H](C)CC)CC1=CC=CC=C1 LRAUKBMYHHNADU-DKIMLUQUSA-N 0.000 claims 1
- AUJWXNGCAQWLEI-KBPBESRZSA-N Phe-Lys-Gly Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCCCN)C(=O)NCC(O)=O AUJWXNGCAQWLEI-KBPBESRZSA-N 0.000 claims 1
- LDEBVRIURYMKQS-WISUUJSJSA-N Ser-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@@H](N)CO LDEBVRIURYMKQS-WISUUJSJSA-N 0.000 claims 1
- KIEIJCFVGZCUAS-MELADBBJSA-N Ser-Tyr-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](CO)N)C(=O)O KIEIJCFVGZCUAS-MELADBBJSA-N 0.000 claims 1
- JVTHIXKSVYEWNI-JRQIVUDYSA-N Thr-Asn-Tyr Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O JVTHIXKSVYEWNI-JRQIVUDYSA-N 0.000 claims 1
- 102100035284 Tumor necrosis factor receptor superfamily member 6B Human genes 0.000 claims 1
- PEVVXUGSAKEPEN-AVGNSLFASA-N Tyr-Asn-Glu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O PEVVXUGSAKEPEN-AVGNSLFASA-N 0.000 claims 1
- BIVIUZRBCAUNPW-JRQIVUDYSA-N Tyr-Thr-Asn Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(O)=O BIVIUZRBCAUNPW-JRQIVUDYSA-N 0.000 claims 1
- 210000004102 animal cell Anatomy 0.000 claims 1
- 230000007910 cell fusion Effects 0.000 claims 1
- 108010020688 glycylhistidine Proteins 0.000 claims 1
- 108010087823 glycyltyrosine Proteins 0.000 claims 1
- 210000004408 hybridoma Anatomy 0.000 claims 1
- 230000036039 immunity Effects 0.000 claims 1
- 108010064235 lysylglycine Proteins 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- 210000004988 splenocyte Anatomy 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 3
- 241000700605 Viruses Species 0.000 abstract description 2
- 108090000623 proteins and genes Proteins 0.000 abstract 2
- 230000002163 immunogen Effects 0.000 abstract 1
- 102000004196 processed proteins & peptides Human genes 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 description 3
- 125000003275 alpha amino acid group Chemical group 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/08—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses
- C07K16/10—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses from RNA viruses
- C07K16/1036—Retroviridae, e.g. leukemia viruses
- C07K16/1045—Lentiviridae, e.g. HIV, FIV, SIV
- C07K16/1063—Lentiviridae, e.g. HIV, FIV, SIV env, e.g. gp41, gp110/120, gp160, V3, PND, CD4 binding site
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
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- General Health & Medical Sciences (AREA)
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- Medicinal Chemistry (AREA)
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- Oncology (AREA)
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- Proteomics, Peptides & Aminoacids (AREA)
- AIDS & HIV (AREA)
- Engineering & Computer Science (AREA)
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- Chemical Kinetics & Catalysis (AREA)
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- General Engineering & Computer Science (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Description
Claims (20)
- 사람 면역 결핍 바이러스(HIV)의 외피막상에 분자량이 약 1.2 ×105달톤 인 당단백 항원(gp120)의 제3가변부(V3)에 주요 중화영역(PND) 내에 아미노산 서열 : Xa1-G1y-Pro-Xa2-Arg-Xa3[식중, Xal은, Ala, Ile, Leu, Met, Asn, Pro, Gin, Ser, Thr, Val, Tyr 이고; Xa2는 Gly, Ala이고; Xa3은 Ala, Cys, Asp, Glu, Gly, His, Ile, Lys, Leu, Met, Asn, Gin, Arg, Ser, Thr, Val, Trp, Tyr이다]에 의해 정의되는 영역을 갖는 HIV를 중화시킬 수 있는 모노클론 항체, 또는 그의 단편.
- 제1항에 있어서, 상기 주요 중화 영역(PND) 내에 아미노산 서열 : Xaa-Gly-Pro-Gly-Arg-Ala[식중, Xaa는 Ala, Ile, Leu, Met, Asn, Pro, Gin, Ser, Thr, Val, Tyr 이다.]; Ile-Gly-Pro-Arg-Xaa [식중, Xaa 는 Ala, Cys, Asp, Glu, Gly, His, Ile, Lys, Leu, Met, Asn, Gin, Arg, Ser, Thr, Val, Trp, Tyr이다]; Val-Gly-Pro-Gly-Arg-Thr; Val -Gly-Pro-Gly-Arg-Ser; 또는 Ile-Gly-Pro-Ala-Arg-Ala에 의해 정의되는 영역을 갖는 HIV를 중화시킬 수 있는 모노클론 항체. 또는 그의 단편.
- 제1항 또는 제3항에 있어서, H사슬 가변부의 상보성 결정 영역(CDR1 내지 CDR3)의 아미노산 서열이 하기의 서열 : CDR1 : Asn Ser Trp Ile Gly, CDR2 : Asp Ile Tyr Pro Gly Gly Gly Tyr Thr Asn Tyr Asn Glu Ile Phe Lys Gly, CDR3 : Gly Ile Pro Gly Tyr Ala Met Asp Tyr을 갖는 모노클론 항체 또는 그의 단편.
- 제3항에 있어서, H사슬 가변부의 아미노산 서열이 서열표서열 번호 : 1에 나타난 바와 같은 아미노산 서열인 모노클론 항체 또는 그의 단편.
- 제1항 내지 제2항에 있어서, L사슬 가변부의 상보성 결정 영역(CDR1 내지 CDR3)의 아미노산 서열이 하기의 서열 : CDR1 : Lys Ser Ser Gin Ser Leu Leu Asn Ser Gly Asp Gin Lys Asn Tyr Leu Thr, CDR2 : Trp Ala Ser Thr Gly Glu Ser, CDR3 : Gin Aan Asp Tyr Ser Tyr Pro Trp Thr을 갖는 모노클론 항체 또는 그의 단면.
- 제5항에 있어서, L사슬 가변부의 아미노산 서열이 서열포서열 번호 : 3에 나타난 바와 같은 아미노산 같은 아미노산 서열인 모노클론 항체 또는 그의 단편.
- 제1항 내지 제6항 중의 어느 한 항에 있어서, 공업기술원 생명공학 공업기술 연구소에 수탁 번호 FERM BP-4561로 기탁되어 있는 하이브리도마에 의해 제조되는 모노클론 항체 또는 그의 단편.
- Gly-Pro-Gly-Arg 서열을 포함하는 펩티드로 일차 면역하고, Gly-Pro-Gly-Arg서열을 포함하는 다른 펩티드로 2차 면역 및 이하 추가 면역시켜 수득한 비장 세포를, 세포 융합 물질로서, 사용하여 세포 융합을 수행하는 것을 특징으로 하는, 사람 면역결핍 바이러스(HIV)의 외피막상에 분자량이 약 1.2 ×105달톤 인 당단백 항원(gp120)의 제3가변부(V3)에 주요 중화 영역(PND) 내에 아미노산 서열 : Xal-Gly-Pro-Xa2-Arg-xA3 [식중, Xal은, Ala, Ile, Leu, Met, Asn, Pro, Gin, Ser, Thr, Val, Tyr이고; Xa2는 Gly, Ala이고; Xa3은 Ala, Cys, Asp, Glu, Gly His, Ile, Lys, Leu, Met, Asn, Gin, Arg, Ser Thr, Val, Trp, Tyr이다]에 의해 정의되는 영역을 갖는 HIV를 중화시킬 수 있는 모노클론 항체, 또는 그의 단편의 제조 방법.
- 사람 면역결핍 바이러스(HIV)의 외치막상에 분자량이 약 1.2 ×105달톤 인 당단백 항원(gp120)의 제3가변부(V3)에 주요 중화영역(PND)내에 아미노산 서열 : Xal-Gly- Pro-Xa2-Arg-Xa3 [식중,Xal은, Ala, Ile, Leu, Met, Asn, Pro, Gin, Ser, Thr, Val, Tyr이고 ; Xa2는 Gly, Ala이고; Xa3은 Ala, Cys, Asp, Glu, Gly, His, Ile, Lys, Leu, Met, Asn, Gin, Arg, Ser, Thr, Val, Trp, Tyr이다]에 의해 정의되는 영역을 갖는 HIV를 중화시킬 수 있으며; 최소한 가변부의 상보성 결정 영역이 마우스 항체로 부터 유래되고 남아있는 영역은 사람 항체로 부터 유래되는 재조합 항- HIV항체의 H사슬.
- 제9항에 있어서, 상기 PND 내에 아미노산 서열 : Xaa-Gly-Pro-Gly-Arg-Ala[식중, Xaa는 Ala, Ile, Leu, Met, Asn, Pro, Gin, Ser, Thr, Val, Tyr 이다]; Ile-Gly-Pro-Gly-Arg-Xaa [식중, Xaa는 Ala, Cys, Asp, Glu, Gly, His, Ile, Lys, Leu, Met, Asn, Gin, Arg, Ser, Thr, Val, Trp, Tyr이다]; Val -Gly-Pro-Gly-Arg-Thr; Val-Gly-Pro-Gly-Arg-Ser; 또는 Ile-Gly-Pro-Ala-Arg-Ala에 의해 정의되는 영역을 갖는 HIV를 중화시킬 수 있는, 재조합 형-HIV항체의 H사슬.
- 제9항 또는 제10항에 있어서, H사슬 가변부의 상보성 결정 영역(CDR1 내지 CDR3)의 아미노산 서열이 하기의 서열; CDR1 : Asn Ser Trp Ile Gly, CDR2 : Asp Ile Tyr Pro Gly Gly Gly Tyr Thr Asn Tyr Asn Glu Ile Phe Lys Gly, CDR3 : Gly Ile Pro Gly Tyr Ala Met Asp Tyr 을 갖는 재조합 항-HIV항체의 H사슬.
- 제11항에 있어서, 키메라성 항체의 H사슬이며, H사슬 가변부의 아미노산 서열이 서열표 서열 번호 : 1에 기재된 바와 같은 아미노산 순위 1∼118의 아미노산 서열인 재조합 항-HIV항체의 H사슬.
- 제11항에 있어서, 인간화 항체의 H사슬이며, H사슬 가변부의 아미노산 서열이 서열표 서열 번호 : 2에 기재된 바와 같은 아미노산 순위 1∼118의 아미노산 서열인 재조합 항-HIV항체의 H사슬.
- 사람 면역 결핍 바이러스(HIV)의 외피막상에 분자량이 약 1.2 ×105달톤 인 당단백 항원(gp120)의 제3가변부(V3)에 주요 중화영역(PND) 내에 아미노산 서열 : Xal-Gly-Pro-Xa2-Arg-Xa3 [식중, Xal은, Ala, Ile, Leu, Met, Asn, Pro, Gin, Ser, Thr, Val, Tyr이고; Xa2는 Gly, Ala이고; Xa3은 Ala, Cys, Asp, Glu, Gly, His, Ile, Lys, Leu, Met, Asn, Gin, Arg, Ser, Thr, Val, Trp, Tyr이다]에 의해 정의되는 영역을 갖는 HIV를 중화시킬 수 있으며; 최소한 가변부의 상보성 결정 영역은 마우스 항체로 부터 유래되고 남아있는 영역은 사람 항체로 부터 유래되는 재조합 항-HIV항체의 L사슬.
- 제14항에 있어서, 상기 PND 내에 아미노산 서열 : Xaa-Gly-Pro-Gly-Arg-Ala [식중, Xaa는 Ala, Ile, Leu, Met, Asn, Pro, Gin, Ser, Thr, Val, Tyr이다.]; Ile-Gly-Pro-Gly-Arg-Xaa [식중, Xaa는 Ala, Cys, Asp, Glu, Gly, His, Ile, Lys, Leu, Met, Asn, Gin, Arg, Ser, Thr, Val, Trp, Tyr이다]; Val-Gly-Pro-Gly-Arg-Thr; Val-Gly-Pro-Gly-Arg-Ser; 또는 Ile-Gly-Pro-Ala-Arg-Ala에 의해 정의되는 영역을 갖는 HIV를 중화시킬 수 있는, 재조합 항-HIV항체의 L사슬.
- 제14항 또는 제15항에 있어서, H사슬 가변부의 상보성 결정 영역(CDR1 내지 CDR3)의 아미노산 서열이 하기의 서열 : CDR1 : Lys Ser Ser Gin Ser Leu Leu Asn Ser Gly Asp Gin Lys Asn Tyr Leu Thr, CDR2 : Trp Ala Ser Thr Gly Glu Ser, DCR3 : Gin Asn Asp Tyr Ser Tyr Pro Trp Thr을 갖는 재조합 항-HIV항체의 H사슬.
- 제16항에 있어서, 카메라성 항체의 L사슬이며, 가변부의 아미노산 서열이 서열표 서열 번호 : 3에 기재된 바와 같은 아미노산 순위 1∼113의 아미노산 서열인 재조합 항-HIV항체의ㅡ L사슬.
- 제9항에서 청구된 재조합 항-HIV항체의 H사슬 및 제14항에 청구된 재조합 항-HIV 항체의 L사슬을 포함하는 재조합 항-HIV항체.
- 제9항에서 청구된 재조합 항-HIV항체의 H사슬 및 제14항에 청구된 재조합 항-HIV 항체의 L사슬을 포함하는 재조합 항-HIV항체.
- 제19항에서 청구된 재조합 항-HIV항체를 발현할 수 있는 발현 벡터의 구축, 동물 세포내에서 상기 발현백터의 발현, 및 상기 항체의 수합을 포함하는 것을 특징으로 하는 항-HIV항체의 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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JP93-78913 | 1993-03-11 | ||
JP7891393 | 1993-03-11 | ||
PCT/JP1994/000371 WO1994020632A1 (en) | 1993-03-11 | 1994-03-09 | Anti-hiv monoclonal antibody |
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JP (1) | JP3855071B2 (ko) |
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AT (1) | ATE256751T1 (ko) |
AU (1) | AU681633B2 (ko) |
DE (1) | DE69433422T2 (ko) |
DK (1) | DK0690132T3 (ko) |
ES (1) | ES2213148T3 (ko) |
PT (1) | PT690132E (ko) |
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1994
- 1994-03-09 DK DK94909286T patent/DK0690132T3/da active
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Also Published As
Publication number | Publication date |
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ES2213148T3 (es) | 2004-08-16 |
DK0690132T3 (da) | 2004-04-13 |
EP0690132A4 (en) | 1998-07-29 |
EP0690132B1 (en) | 2003-12-17 |
DE69433422T2 (de) | 2004-09-16 |
JP3855071B2 (ja) | 2006-12-06 |
DE69433422D1 (de) | 2004-01-29 |
US6114143A (en) | 2000-09-05 |
EP0690132A1 (en) | 1996-01-03 |
KR100337069B1 (ko) | 2002-10-11 |
ATE256751T1 (de) | 2004-01-15 |
PT690132E (pt) | 2004-04-30 |
WO1994020632A1 (en) | 1994-09-15 |
AU6219494A (en) | 1994-09-26 |
AU681633B2 (en) | 1997-09-04 |
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