KR960700692A - 면역 반응의 강화 방법(immunological response potentiation process) - Google Patents
면역 반응의 강화 방법(immunological response potentiation process) Download PDFInfo
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- KR960700692A KR960700692A KR1019950703557A KR19950703557A KR960700692A KR 960700692 A KR960700692 A KR 960700692A KR 1019950703557 A KR1019950703557 A KR 1019950703557A KR 19950703557 A KR19950703557 A KR 19950703557A KR 960700692 A KR960700692 A KR 960700692A
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/002—Protozoa antigens
- A61K39/015—Hemosporidia antigens, e.g. Plasmodium antigens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/02—Bacterial antigens
- A61K39/08—Clostridium, e.g. Clostridium tetani
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
- A61K9/1647—Polyesters, e.g. poly(lactide-co-glycolide)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
- A61K2039/55511—Organic adjuvants
- A61K2039/55555—Liposomes; Vesicles, e.g. nanoparticles; Spheres, e.g. nanospheres; Polymers
Abstract
합성되었거나 생리적으로 상승되어 면역성이 낮은 항원을 강화하기 위해 면역반응 강화 방법이 개발되었다. 항원은 생물분해서 미립자속으로 투입되고, 이 항원을 함유한 미립자는 다시 매개 속으로 확산되는데 이 분산매가 주사로 투여될 때 수양성 항원용액과 비교해 볼때 더욱 강화된 항체 즉 TB-임파구세포와 TC-임파구 세포반응을 촉진시킨다. 면역강화의 정도는 적어도 IFA방식에 의해 얻어진 면역강화 정도와 비교될 수 있다. 선형 B-TH-세포 에피토프, 선형 TC-세포-에피토프, 이 두가지 에피토프의 이합체(dimer)와 다합체(multimer) 등은 그 결합물과 마찬가지로 면역성이 약한 항원으로 이용된다. 미립자는 다양한 습윤제(wettabilities), 팽창제를 혼합시킴으로서 릴리스(release)와 생물분해 시간을 달성할 수 있다. 이 공정은 바이러스, 박테리아, 원충 또는 종양세포로 인해 발병된 인간과 동물의 질병을 면역시키는데 효력을 발휘한다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (12)
- 합성항원에 대한 사람과 동물의 면역반응의 강화를 위한 방법은 다음과 같은 특징을 가진다; 합성항원은 먼저 분해성 구형 미립자에 투여시킨다. 그후에 합성항원을 함유한 미립자는 분산매속에서 현탁된다. 이 조합체를 주사로 투여하여 강화된 면역반응이 일어난다.
- 청구의 범위 제1항에 따른 방법의 특징은 합성항원으로 적어도 하나의 B-세포 에피토프와 TH-세포-에피토프를 가진 단순한 체인(chain)로 구성된 결합물을 사용한다는 점이다.
- 청구의 범위 제1항에 따른 방법의 특징은 합성항원으로 반복적 공유결합된 B-세포-에피토프와 TH-세포-에피토프로 구성된 결합물을 사용한다는 점이다.
- 청구의 범위 제1항에 따른 방법의 특징은 합성항원으로 세균독성 T-세포-에피토프(TC)로 구성된 혼합물을 사용한다는 점이다.
- 청구의 범위 제1항에 따른 방법의 특징은 합성항원으로 적어도 하나의 TH-에피토프와 적어도 하나의 TC-에피토프의 결합물을 사용한다는 점이다.
- 청구의 범위 제1∼5항 까지의 방법의 특징은 합성항원의 원충, 바이러스, 박테리아 또는 종양세포에서 유래한 B-세포 에피토프와 T-세포-에피토프를 함유하고 있다는 것이다.
- 청구의 범위 제1∼5항에 따른 방법의 특징은 합성항원의 원충, 바이러스, 박테리아, 종양세포 또는 이러한 것들의 임의적 결합물에서 나온 B-세포 에피토프와 T-세포-에피토프를 포함하고 있다는 점이다.
- 청구의 범위 제1∼7에 따른 방법의 특징은 구형미립자가 적합한 분해성 생물 폴리어로 만들어졌다는 것이며, 생물폴리어는 폴리(유산), 폴리(글리코산), 폴리(유산-CO 글리코산), 폴리오르토에스레(poly orthoester) 및 다무수화합물(poly anhydrie)의 그룹에서 유래한다는 점이다.
- 청구의 범위 8에 따른 방법의 특징은 생물폴리어가 적어도 2개의 서로 다른 그룹에서 유래한다는 점이다.
- 청구의 범위 제1∼9항에 따른 방법의 특징은 수성이나 유성의 레시틴 용액이나 또는 수성-유성 레시틴-유탁액이 분산매로 사용된다는 점이다.
- 청구의 범위 1∼9항에 따른 방법의 특징은 분산매로서 미소 유제를 사용한다는 점이다.
- 바이러스, 박테리아, 원충, 종양세포에 의해 발생된 질병에 대해 인간과 동물의 면역화에 청구의 범위 제1∼11항에 따른 방법을 적용한다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH384993 | 1993-12-23 | ||
CH3849/93-6 | 1993-12-23 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR960700692A true KR960700692A (ko) | 1996-02-24 |
KR100372375B1 KR100372375B1 (ko) | 2003-04-21 |
Family
ID=4264801
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019950703557A KR100372375B1 (ko) | 1993-12-23 | 1994-12-23 | 면역반응의강화방법 |
Country Status (12)
Country | Link |
---|---|
US (1) | US6596278B2 (ko) |
EP (1) | EP0686030B1 (ko) |
JP (1) | JPH08507088A (ko) |
KR (1) | KR100372375B1 (ko) |
CN (1) | CN1120809A (ko) |
AT (1) | ATE199316T1 (ko) |
AU (1) | AU1217395A (ko) |
CA (1) | CA2156718A1 (ko) |
DE (1) | DE59409668D1 (ko) |
DK (1) | DK0686030T3 (ko) |
ES (1) | ES2156932T3 (ko) |
WO (1) | WO1995017167A1 (ko) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
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US6270795B1 (en) | 1995-11-09 | 2001-08-07 | Microbiological Research Authority | Method of making microencapsulated DNA for vaccination and gene therapy |
EP0965336A1 (en) | 1995-11-09 | 1999-12-22 | Microbiological Research Authority | Microencapsulated DNA for gene therapy |
US5783567A (en) * | 1997-01-22 | 1998-07-21 | Pangaea Pharmaceuticals, Inc. | Microparticles for delivery of nucleic acid |
WO1999002183A2 (en) * | 1997-07-10 | 1999-01-21 | Ctl Immunotherapies Corporation | A method of inducing a ctl response |
US6977074B2 (en) | 1997-07-10 | 2005-12-20 | Mannkind Corporation | Method of inducing a CTL response |
US6994851B1 (en) | 1997-07-10 | 2006-02-07 | Mannkind Corporation | Method of inducing a CTL response |
GB9810236D0 (en) | 1998-05-13 | 1998-07-08 | Microbiological Res Authority | Improvements relating to encapsulation of bioactive agents |
US6406719B1 (en) | 1998-05-13 | 2002-06-18 | Microbiological Research Authority | Encapsulation of bioactive agents |
WO1999065531A1 (en) | 1998-06-18 | 1999-12-23 | Johns Hopkins University School Of Medicine | Polymers for delivery of nucleic acids |
ATE452651T1 (de) | 1998-09-01 | 2010-01-15 | Merrion Res Iii Ltd | Orale impfstoff-zusammensetzung |
US7087236B1 (en) | 1998-09-01 | 2006-08-08 | Merrion Research I Limited | Method for inducing a cell-mediated immune response and improved parenteral vaccine formulations thereof |
EP2351576A1 (en) * | 2004-12-29 | 2011-08-03 | Mannkind Corporation | Methods to trigger, maintain and manipulate immune responses by targeted administration of biological response modifiers into lymphoid organs |
US8202523B2 (en) * | 2005-09-22 | 2012-06-19 | ProSci, Inc. | Glycosylated polypeptides produced in yeast mutants and methods of use thereof |
JP2009512729A (ja) * | 2005-10-24 | 2009-03-26 | スタヴァル ファーマ リミテッド | 菌類及び細菌を処理、抑制、殺滅する方法 |
AR064862A1 (es) * | 2007-01-15 | 2009-04-29 | Glaxosmithkline Biolog Sa | Proteinas de fusion que comprenden un antigeno de rechazo tumoral prame (dage) |
US20090004213A1 (en) | 2007-03-26 | 2009-01-01 | Immatics Biotechnologies Gmbh | Combination therapy using active immunotherapy |
EP2575869B1 (en) * | 2010-06-04 | 2017-07-26 | Flow Pharma Inc. | Peptide particle formulation |
CN102901814B (zh) * | 2012-07-12 | 2014-11-26 | 浙江大学 | 莠去津分子印迹金标试纸条及其用途 |
Family Cites Families (16)
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US4599230A (en) * | 1984-03-09 | 1986-07-08 | Scripps Clinic And Research Foundation | Synthetic hepatitis B virus vaccine including both T cell and B cell determinants |
US5417986A (en) | 1984-03-16 | 1995-05-23 | The United States Of America As Represented By The Secretary Of The Army | Vaccines against diseases caused by enteropathogenic organisms using antigens encapsulated within biodegradable-biocompatible microspheres |
US5762965A (en) * | 1984-03-16 | 1998-06-09 | The United States Of America As Represented By The Secretary Of The Army | Vaccines against intracellular pathogens using antigens encapsulated within biodegradble-biocompatible microspheres |
US4803070A (en) | 1986-04-15 | 1989-02-07 | Ribi Immunochem Research Inc. | Immunological emulsion adjuvants for polysaccharide vaccines |
US4962091A (en) * | 1986-05-23 | 1990-10-09 | Syntex (U.S.A.) Inc. | Controlled release of macromolecular polypeptides |
US5008116A (en) * | 1988-11-14 | 1991-04-16 | Frederick Cahn | Immunostimulatory microsphere |
JP3233402B2 (ja) | 1989-11-13 | 2001-11-26 | サイオス ノバ インコーポレイテッド | 物質の制御送達用のリポスフェア |
AU8303691A (en) * | 1991-04-24 | 1992-12-21 | United States Of America, As Represented By The Secretary Of The Army, The | Oral-intestinal vaccines against diseases caused by enteropathogenic organisms using antigens encapsulated within biodegradable-biocompatible microspheres |
FR2695563B1 (fr) * | 1992-09-11 | 1994-12-02 | Pasteur Institut | Microparticules portant des antigènes et leur utilisation pour l'induction de réponses humorales ou cellulaires. |
US6004763A (en) | 1992-09-11 | 1999-12-21 | Institut Pasteur | Antigen-carrying microparticles and their use in the induction of humoral or cellular responses |
WO1994015635A1 (en) * | 1993-01-11 | 1994-07-21 | Dana-Farber Cancer Institute | Inducing cytotoxic t lymphocyte responses |
US5879687A (en) * | 1994-04-22 | 1999-03-09 | Corixa Corporation | Methods for enhancement of protective immune responses |
DK0991403T3 (da) | 1997-01-30 | 2003-07-28 | Chiron Corp | Anvendelse af mikropartikler med adsorberet antigen til stimulering af immunresponser |
US6312731B1 (en) | 1997-08-29 | 2001-11-06 | Southern Research Institute | Rapid release encapsulated bioactive agents for inducing or potentiating an immune response and methods of using thereof |
PT1042001E (pt) | 1997-12-16 | 2002-09-30 | Chiron Corp | Uso de microparticulas combinadas com emulsoes submicronicas oleo-em-agua |
ATE322285T1 (de) | 1998-09-01 | 2006-04-15 | Elan Corp Plc | Verfahren zur induktion der zellulären immunantwort und parenterale impfstoff- zusammensetzungen dazu |
-
1994
- 1994-12-23 AT AT95903221T patent/ATE199316T1/de not_active IP Right Cessation
- 1994-12-23 CA CA002156718A patent/CA2156718A1/en not_active Abandoned
- 1994-12-23 WO PCT/CH1994/000242 patent/WO1995017167A1/de active IP Right Grant
- 1994-12-23 AU AU12173/95A patent/AU1217395A/en not_active Abandoned
- 1994-12-23 CN CN94191709A patent/CN1120809A/zh active Pending
- 1994-12-23 KR KR1019950703557A patent/KR100372375B1/ko not_active IP Right Cessation
- 1994-12-23 JP JP7517077A patent/JPH08507088A/ja not_active Ceased
- 1994-12-23 DK DK95903221T patent/DK0686030T3/da active
- 1994-12-23 EP EP95903221A patent/EP0686030B1/de not_active Expired - Lifetime
- 1994-12-23 US US08/507,323 patent/US6596278B2/en not_active Expired - Fee Related
- 1994-12-23 DE DE59409668T patent/DE59409668D1/de not_active Expired - Fee Related
- 1994-12-23 ES ES95903221T patent/ES2156932T3/es not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
DE59409668D1 (de) | 2001-04-05 |
EP0686030B1 (de) | 2001-02-28 |
AU1217395A (en) | 1995-07-10 |
CN1120809A (zh) | 1996-04-17 |
CA2156718A1 (en) | 1995-06-29 |
US20020041879A1 (en) | 2002-04-11 |
ES2156932T3 (es) | 2001-08-01 |
US6596278B2 (en) | 2003-07-22 |
EP0686030A1 (de) | 1995-12-13 |
ATE199316T1 (de) | 2001-03-15 |
WO1995017167A1 (de) | 1995-06-29 |
KR100372375B1 (ko) | 2003-04-21 |
DK0686030T3 (da) | 2001-06-25 |
JPH08507088A (ja) | 1996-07-30 |
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