KR970705403A - 비독성 경구용 어쥬번트로써 효과적인 장독소 돌연변이체(mutant enterotoxin effective as a non-toxic oral adjuvant) - Google Patents
비독성 경구용 어쥬번트로써 효과적인 장독소 돌연변이체(mutant enterotoxin effective as a non-toxic oral adjuvant)Info
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- KR970705403A KR970705403A KR1019970701224A KR19970701224A KR970705403A KR 970705403 A KR970705403 A KR 970705403A KR 1019970701224 A KR1019970701224 A KR 1019970701224A KR 19970701224 A KR19970701224 A KR 19970701224A KR 970705403 A KR970705403 A KR 970705403A
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- vaccine
- composition
- antigen
- enterotoxin
- coli heat
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- 239000000147 enterotoxin Substances 0.000 title claims abstract 13
- 231100000655 enterotoxin Toxicity 0.000 title claims abstract 13
- 101710146739 Enterotoxin Proteins 0.000 title claims abstract 12
- 239000002671 adjuvant Substances 0.000 title claims 4
- 231100000252 nontoxic Toxicity 0.000 title 2
- 230000003000 nontoxic effect Effects 0.000 title 2
- 241000588724 Escherichia coli Species 0.000 claims abstract 11
- 239000000427 antigen Substances 0.000 claims abstract 9
- 102000036639 antigens Human genes 0.000 claims abstract 9
- 108091007433 antigens Proteins 0.000 claims abstract 9
- 230000028993 immune response Effects 0.000 claims abstract 5
- 239000000203 mixture Substances 0.000 claims 13
- 229960005486 vaccine Drugs 0.000 claims 10
- 238000000034 method Methods 0.000 claims 9
- 230000000694 effects Effects 0.000 claims 7
- 230000001580 bacterial effect Effects 0.000 claims 5
- 102000004142 Trypsin Human genes 0.000 claims 4
- 108090000631 Trypsin Proteins 0.000 claims 4
- 230000001681 protective effect Effects 0.000 claims 4
- 239000012588 trypsin Substances 0.000 claims 4
- 102000004190 Enzymes Human genes 0.000 claims 3
- 108090000790 Enzymes Proteins 0.000 claims 3
- 150000001413 amino acids Chemical class 0.000 claims 3
- 239000000568 immunological adjuvant Substances 0.000 claims 3
- 230000000968 intestinal effect Effects 0.000 claims 3
- 231100000331 toxic Toxicity 0.000 claims 3
- 230000002588 toxic effect Effects 0.000 claims 3
- 108010055044 Tetanus Toxin Proteins 0.000 claims 2
- 230000000240 adjuvant effect Effects 0.000 claims 2
- 238000003556 assay Methods 0.000 claims 2
- 229930186900 holotoxin Natural products 0.000 claims 2
- 229940041323 measles vaccine Drugs 0.000 claims 2
- 244000052769 pathogen Species 0.000 claims 2
- 230000001717 pathogenic effect Effects 0.000 claims 2
- 229940118376 tetanus toxin Drugs 0.000 claims 2
- 102000009062 ADP Ribose Transferases Human genes 0.000 claims 1
- 108010049290 ADP Ribose Transferases Proteins 0.000 claims 1
- 239000004475 Arginine Substances 0.000 claims 1
- 241000894006 Bacteria Species 0.000 claims 1
- 241000589876 Campylobacter Species 0.000 claims 1
- 206010008631 Cholera Diseases 0.000 claims 1
- 102000016607 Diphtheria Toxin Human genes 0.000 claims 1
- 108010053187 Diphtheria Toxin Proteins 0.000 claims 1
- 241000233866 Fungi Species 0.000 claims 1
- 229940033330 HIV vaccine Drugs 0.000 claims 1
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 claims 1
- 241000204031 Mycoplasma Species 0.000 claims 1
- 201000005702 Pertussis Diseases 0.000 claims 1
- 206010057190 Respiratory tract infections Diseases 0.000 claims 1
- 229940124859 Rotavirus vaccine Drugs 0.000 claims 1
- 102000004357 Transferases Human genes 0.000 claims 1
- 108090000992 Transferases Proteins 0.000 claims 1
- 241000607598 Vibrio Species 0.000 claims 1
- 241000700605 Viruses Species 0.000 claims 1
- 244000052616 bacterial pathogen Species 0.000 claims 1
- 229960005004 cholera vaccine Drugs 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 230000000688 enterotoxigenic effect Effects 0.000 claims 1
- SPSXSWRZQFPVTJ-ZQQKUFEYSA-N hepatitis b vaccine Chemical compound C([C@H](NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CCSC)C(=O)N[C@@H](CC1N=CN=C1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)OC(=O)CNC(=O)CNC(=O)[C@H](C)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@@H](N)CCCNC(N)=N)C1=CC=CC=C1 SPSXSWRZQFPVTJ-ZQQKUFEYSA-N 0.000 claims 1
- 229940124736 hepatitis-B vaccine Drugs 0.000 claims 1
- 230000002163 immunogen Effects 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 229960003971 influenza vaccine Drugs 0.000 claims 1
- 229940124735 malaria vaccine Drugs 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 244000000010 microbial pathogen Species 0.000 claims 1
- 229940095293 mumps vaccine Drugs 0.000 claims 1
- 229960002566 papillomavirus vaccine Drugs 0.000 claims 1
- 244000045947 parasite Species 0.000 claims 1
- 239000013612 plasmid Substances 0.000 claims 1
- 229960001539 poliomyelitis vaccine Drugs 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 210000002966 serum Anatomy 0.000 claims 1
- 239000003053 toxin Substances 0.000 claims 1
- 231100000765 toxin Toxicity 0.000 claims 1
- 229940124856 vaccine component Drugs 0.000 claims 1
- 229940021648 varicella vaccine Drugs 0.000 claims 1
- 230000001900 immune effect Effects 0.000 abstract 1
- 229940126578 oral vaccine Drugs 0.000 abstract 1
- 230000001988 toxicity Effects 0.000 abstract 1
- 231100000419 toxicity Toxicity 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/24—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Enterobacteriaceae (F), e.g. Citrobacter, Serratia, Proteus, Providencia, Morganella, Yersinia
- C07K14/245—Escherichia (G)
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- A61K39/0258—Escherichia
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- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/54—Medicinal preparations containing antigens or antibodies characterised by the route of administration
- A61K2039/541—Mucosal route
- A61K2039/542—Mucosal route oral/gastrointestinal
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- A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
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Abstract
독성은 상실하였으나 이의 면역학적 활성은 보유하고 있는 대장균 열-불안정한 장독소의 신규한 돌연변이 형으로된 조성물과 이의 용도를 제공한다. 이와 같은 장독소는 경구 백신 준비물의 일부로써 투여하였을 때 항원에 대한 증가된 면역반응을 얻기 위해 무관한 항원과 복합하여 사용될 수도 있다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (22)
- 면역학적 어쥬번트 활성을 가지면서 NAD-아그마틴-ADP-리보실 전달효소 검사에 의해 측정하였을 때 ADP-리보실화 효소활성이 부족한 대장균 열-불안정한 장독소 할로톡신의 돌연변이 형으로 구성된 것을 특징으로 하는 조성물.
- 할로톡신의 A 소단위가 트립신에 의해 절단되진 않은 면역학적 어쥬벤트 활성이 있는 대장균 열 불안정한 장독소 할로톡신의 돌연변이 형으로 구성된 것을 특징으로 하는 조성물.
- 제1항 또는 제2항에 있어서, 조성물은 대장균 열-불안정한 장독소의 A 소단위와 B 소단위 모드를 발현하고 ATCC에 기탁되어 기탁번호가 696883인 대장균 LTR192G에 포함된 플라스미드 pBD95에 의해 인코드되는 것을 특징으로 하는 조성물.
- 제1항 내지 2항에 따른 조성물과 복합된 항원으로 구성된 것을 특징으로 하는 백신 조성물.
- 제4항에 있어서, 항원은 인플루엔자 백신, 바리셀라 백신, 디프테리아 독소, 테타누스 독소, 페로트시스 백신 일본 엔세팔리티스 백신, 페르투시스, 디프테이아와 테타느스독소의 혼합형 백신, 라임 질병백신, 폴리오백신, 말라리아 백신, 허피스 백신, HIV 백신, 파필로마 바이러스 백신, 헤파타이티스 B백신, 로타 백신, 캄필로박터 백신,콜레라 백신,장병원성 대장균 백신, 장독소 대장균 백신, 쉬스토소마이시스 백신, 홍역 백신, 루베라 백신, 멈프스 백신, 홍역, 루벨라와 멈프스 혼합형 백신 그리고 미코플라스마 백신에서 선택되는 것을 특징으로 하는 백신 조성물.
- 숙주에서 병원균에 보호성 면역반응을 만드는데 유용한 조성물에 있어서, 제1항 또는 2항에 따른 조성물의 어쥬번트 효과량과 항원 효과량의 혼합물로 구성된 것을 특징으로 하는 조성물.
- 병원균에 대한 숙주에서 보호성 면역 반응을 만드는데 유용한 키트에 있어서, 두가지 성분으로 구성되는 데 a) 효과량의 항원과 b) NAD-아크마틴 ADP-리보실전달 효소 검사에 의해 측정하였을 때 ADP-리보실화 효소 활성이 부족하나 면역학적 어쥬번트 활성을 가지는 대장균 열-불안정한 장독소 홀로톡신 돌연변이체의 어쥬번트 효과량으로 구성되고 이때, 이 두성분을 경구을 투여가능한 담체에 있고 서로 혼합시킨후 함께 투여하거나 또는 짧은 시간 간격내에서 별도로 투여될 수 있는 것을 특징으로 하는 키트.
- 제1항 또는 6항에 있어서, A소단위는 트립신에 의해 절단되지 않는 것을 특징으로 하는 조성물.
- 제4항에 있어서, A소단위는 트립신에 의해 절단되지 않는 것을 특징으로 하는 키트.
- 제7항에 있어서, A소단위는 트립신에 의해 절단되지 않는 것을 특징으로 하는 키트.
- 제1항 또는 6항에 있어서, 야생형 대장균 열-불안정한 장독소의 아미노산 Arg192는 Gly192로 대체되는 것을 특징으로 하는 조성물.
- 제4항에 있어서, 야생형 대장균 열-불안정한 장독소의 아미노산 Arg192는 Gly192로 대체되는 것을 특징으로 하는 조성물.
- 제7항에 있어서, 야생형 대장균 열-불안정한 장독소의 아미노산 Arg192는 Gly192로 대체되는 것을 특징으로 하는 조성물.
- 병원균에 대한 숙주에서 보호성 면역 반응을 만드는데 방법에 있어서, 효과량의 항원과 NAD-아크마틴 ADP-리보실전달 효소 검사에 의해 측정하였을 때 ADP-리보실화 효소 활성이 부족하나 면역학적 어쥬번트 활성을 가지는 대장균 열-불안정한 장독소 홀로톡신 돌연변이체의 어쥬번트 효과량을 경구을 투여가능한 담체에 있고 서로 혼합시킨후 함께 투여하는 것을 특징으로 하는 방법.
- 제14항에 있어서, 혈청반응이 생산되는 것을 특징으로 한는 방법.
- 제14항에 있어서, 점막반응이 생산되는 것을 특징으로 한는 방법.
- 제14항에 있어서, 항원이 연속 촉진주사가 제공되는 것을 특징으로 하는 방법.
- 제14항에 있어서, 항원이 박테리아, 바이러스, 프로토조아, 곰팡이, 기생충, 그리고 다른 미생물 병원균에서 유도되는 것을 특징으로 하는 방법.
- 제14항에 있어서, 혼합물은 단일 약량으로 수송되는 것을 특징으로 하는 방법.
- 장독소 발테리아 유기체에 대한 보호성 면역 반응을 유도하는 방법에 있어서, 장독소 박테리아 유기체에 대한 백신성분으로써 mLT를 이용하는 것으로 구성된 것을 특징으로 하는 방법.
- 제20항에 있어서, 장독성 박테리아 유기체는 콜레라-형 독소를 발현하는 장독성 박테리아 유기체에서 선택되는 것을 특징으로 하는 방법.
- 제20항에 있어서, 장독성 박테리아 유기체는 대장균spp와 비브리오 spp에서 선택되는 것을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US08/296,848 US6019982A (en) | 1994-08-26 | 1994-08-26 | Mutant enterotoxin effective as a non-toxic oral adjuvant |
US296,848 | 1994-08-26 |
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KR970705403A true KR970705403A (ko) | 1997-10-09 |
KR100399258B1 KR100399258B1 (ko) | 2003-12-31 |
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KR1019970701224A KR100399258B1 (ko) | 1994-08-26 | 1995-07-18 | 비독성경구용어쥬번트로써효과적인장독소돌연변이체 |
Country Status (22)
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US (2) | US6019982A (ko) |
EP (1) | EP0777490B1 (ko) |
JP (1) | JP3860208B2 (ko) |
KR (1) | KR100399258B1 (ko) |
CN (1) | CN1182868C (ko) |
AT (1) | ATE326231T1 (ko) |
AU (1) | AU709779B2 (ko) |
BR (1) | BR9508633A (ko) |
CA (1) | CA2198586C (ko) |
CZ (1) | CZ298131B6 (ko) |
DE (1) | DE69534992T2 (ko) |
DK (1) | DK0777490T3 (ko) |
ES (1) | ES2265148T3 (ko) |
FI (1) | FI120137B (ko) |
HU (1) | HU222985B1 (ko) |
NO (1) | NO317942B1 (ko) |
NZ (1) | NZ291262A (ko) |
PL (1) | PL182667B1 (ko) |
PT (1) | PT777490E (ko) |
RU (1) | RU2160606C2 (ko) |
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ZA (1) | ZA956412B (ko) |
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JP2849632B2 (ja) * | 1988-04-08 | 1999-01-20 | 社団法人北里研究所 | ワクチン製剤 |
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US6019982A (en) * | 1994-08-26 | 2000-02-01 | The Administrators Of The Tulane Educational Fund | Mutant enterotoxin effective as a non-toxic oral adjuvant |
US6033673A (en) * | 1998-03-18 | 2000-03-07 | The Administrators Of Tulane Educational Fund | Double mutant enterotoxin for use as an adjuvant |
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