HK6096A - Cdna clones coding for polypeptides exhibiting human granulocyte macrophage and eosinophil cellular growth factor activity - Google Patents
Cdna clones coding for polypeptides exhibiting human granulocyte macrophage and eosinophil cellular growth factor activity Download PDFInfo
- Publication number
- HK6096A HK6096A HK6096A HK6096A HK6096A HK 6096 A HK6096 A HK 6096A HK 6096 A HK6096 A HK 6096A HK 6096 A HK6096 A HK 6096A HK 6096 A HK6096 A HK 6096A
- Authority
- HK
- Hong Kong
- Prior art keywords
- polypeptide
- cells
- cell
- vector
- cdna
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/52—Cytokines; Lymphokines; Interferons
- C07K14/53—Colony-stimulating factor [CSF]
- C07K14/535—Granulocyte CSF; Granulocyte-macrophage CSF
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
- C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
-
- 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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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Immunology (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- Biophysics (AREA)
- General Chemical & Material Sciences (AREA)
- Plant Pathology (AREA)
- Gastroenterology & Hepatology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Toxicology (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Physics & Mathematics (AREA)
- Public Health (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Steroid Compounds (AREA)
- Fats And Perfumes (AREA)
- Saccharide Compounds (AREA)
Claims (16)
- Rekombinantes Polypeptid mit der Wirksamkeit des kolonien-stimulierenden Faktors auf menschliche neutrophile Granulocyten, Makrophagen und Eosinophile und mit der Struktur
- Polypeptid gemäß Anspruch 1 ohne eine Signalsequenz.
- Polypeptid gemäß Anspruch 1 oder 2, das glykosyliert ist.
- Polypeptid gemäß Anspruch 1 oder 2, das unglykosyliert ist.
- Polypeptid gemäß einem der vorhergehenden Ansprüche in im wesentlichen reiner Form und im wesentlichen frei von anderen Proteinen hämatopoetischer Säugerzellen.
- Verfahren zur Herstellung eines Polypeptids gemäß einem der Ansprüche 1 bis 5, mit den folgenden Schritten:(a) Bildung eines Vektors, der eine für dieses Polypeptid kodierende Nukleotidsequenz umfaßt, worin die Nukleotidsequenz die Fähigkeit zur Exprimierung in einem den Vektor enthaltenden Wirt aufweist;(b) Einbau des Vektors in den Wirt; und(c) Halten des den Vektors enthaltenden Wirts unter Bedingungen, die für die Expression der Nukleotidsequenz in dieses Polypeptid geeignet sind.
- Verfahren gemäß Anspruch 6, worin die Nukleotidsequenz die Sequenz umfaßt.
- Nukleinsäuresequenz, die für ein Polypeptid gemäß Anspruch 1 oder 2 kodiert.
- Nukleinsäuresequenz gemäß Anspruch 8, umfassend die Nukleotidsequenz
- Vektor, im wesentlichen aus einer DNA-Sequenz des Anspruchs 8 oder 9 bestehend, insbesondere wenn dieser Vektor in einen Mikroorganismus oder eine Zelle eingebaut ist.
- Mikroorganismus oder Zelle, welche(r) mit dem replizierbaren Expressionsvektor des Anspruchs 10 transformiert oder transfiziert ist.
- Verfahren zur Steigerung des Zellwachstums oder der Zelldifferenzierung, bei welchem die Zelle mit einem Polypeptid gemäß einem der Ansprüche 1 bis 5 in Kontakt gebracht wird.
- Verfahren zur Herstellung eines Polypeptids mit der Wirksamkeit des kolonien-stimulierenden Faktors auf menschliche neutrophile Granulocyten, Makrophagen und Eosinophile, welches die Kultivierung eines prokaryotischen Mikroorganismus oder einer eukaryotischen Zelle, welche(r) mit einem Vektor gemäß Anspruch 10 transfiziert oder transformiert worden ist, in einem wäßrigen Nährmedium umfaßt.
- Rekombinantes DNA-Molekül, bestehend aus DNA-Segmenten unterschiedlicher Genome, welche außerhalb lebender Zellen endseitig miteinander verknüpft worden sind und welche die Fähigkeit haben, einen Wirt zu infizieren und in diesem und dessen Nachkommen gehalten zu werden, wobei die vorerwähnte DNA-Sequenz für ein Polypeptid gemäß Anspruch 1 oder 2 kodiert.
- Rekombinantes DNA-Molekül gemäß Anspruch 14, umfassend die DNA-Sequenz
- Pharmazeutische Zubereitung umfassend ein Polypeptid gemäß einem der Ansprüche 1 bis 5 in Verbindung mit einem pharmazeutisch annehmbaren Träger.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67389884A | 1984-11-20 | 1984-11-20 | |
| PCT/US1985/002250 WO1986003225A1 (en) | 1984-11-20 | 1985-11-18 | cDNA CLONES CODING FOR POLYPEPTIDES EXHIBITING HUMAN GRANULOCYTE MACROPHAGE AND EOSINOPHIL CELLULAR GROWTH FACTOR ACTIVITY |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK6096A true HK6096A (en) | 1996-01-19 |
Family
ID=24704538
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK6096A HK6096A (en) | 1984-11-20 | 1996-01-11 | Cdna clones coding for polypeptides exhibiting human granulocyte macrophage and eosinophil cellular growth factor activity |
Country Status (26)
| Country | Link |
|---|---|
| EP (1) | EP0202300B1 (de) |
| JP (1) | JP3038348B2 (de) |
| KR (1) | KR920003822B1 (de) |
| CN (3) | CN1020473C (de) |
| AT (1) | ATE82321T1 (de) |
| AU (1) | AU608741B2 (de) |
| BG (1) | BG60840B2 (de) |
| DE (1) | DE3586826T2 (de) |
| DK (1) | DK174598B1 (de) |
| ES (1) | ES8705470A1 (de) |
| FI (1) | FI103986B (de) |
| GR (1) | GR852786B (de) |
| HK (1) | HK6096A (de) |
| HU (1) | HU213226B (de) |
| IE (1) | IE59581B1 (de) |
| IL (1) | IL77080A (de) |
| LU (1) | LU88360I2 (de) |
| MX (1) | MX9203397A (de) |
| MY (1) | MY101971A (de) |
| NL (1) | NL930120I2 (de) |
| NO (1) | NO862903L (de) |
| NZ (1) | NZ214225A (de) |
| OA (1) | OA08671A (de) |
| PT (1) | PT81513B (de) |
| WO (1) | WO1986003225A1 (de) |
| ZA (1) | ZA858833B (de) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU594014B2 (en) * | 1984-03-21 | 1990-03-01 | Research Corporation Technologies, Inc. | Recombinant DNA molecules |
| UA29377C2 (uk) * | 1984-09-19 | 2000-11-15 | Новартіс Аг | Спосіб отримання білка з активністю колонієстимулювального фактора гранулоцитів та макрофагів(gm-csf) приматів |
| ZA856108B (en) * | 1984-10-29 | 1986-10-29 | Immunex Corp | Cloning of human granulocyte-macrophage colony simulating factor gene |
| AU588819B2 (en) * | 1984-10-29 | 1989-09-28 | Immunex Corporation | Cloning of human granulocyte-macrophage colony stimulating factor gene |
| US5078996A (en) * | 1985-08-16 | 1992-01-07 | Immunex Corporation | Activation of macrophage tumoricidal activity by granulocyte-macrophage colony stimulating factor |
| EP0238655A4 (de) * | 1985-10-03 | 1989-09-11 | Biogen Nv | Menschliche granulozyt-makrophagen-kolonie mit stimulierendem faktor-ähnlichen polypeptid und deren herstellung mit hoher ausbeute in mikrobiellen zellen. |
| JPH0618778B2 (ja) * | 1985-10-04 | 1994-03-16 | 中外製薬株式会社 | 白血球減少症治療剤 |
| US5298603A (en) * | 1985-12-21 | 1994-03-29 | Hoechst Aktiengesellschaft | GM-CSF protein, its derivatives, the preparation of proteins of this type, and their use |
| DE3545568A1 (de) * | 1985-12-21 | 1987-07-16 | Hoechst Ag | Gm-csf-protein, seine derivate, herstellung solcher proteine und ihre verwendung |
| JP2583770B2 (ja) * | 1986-09-17 | 1997-02-19 | 大塚製薬株式会社 | 遺伝子 |
| EP0276846A3 (de) * | 1987-01-29 | 1989-07-26 | Zymogenetics, Inc. | Derivate des koloniestimulierenden Faktors |
| JPS6420097A (en) * | 1987-03-02 | 1989-01-24 | Sumitomo Chemical Co | Human granulocyte-macrophage colony stimulating factor |
| AU621051B2 (en) * | 1987-04-28 | 1992-03-05 | Amgen, Inc. | Method for purifying granulocyte-macrophage colony stimulating factor |
| AU626530B2 (en) * | 1987-07-17 | 1992-08-06 | Schering Biotech Corporation | Human granulocyte-macrophage colony stimulating factor and muteins thereof |
| CA1335717C (en) * | 1987-07-17 | 1995-05-30 | Takashi Yokota | Human granulocyte-macrophage colony stimulating factor and muteins thereof |
| GB2212159B (en) * | 1987-11-13 | 1992-01-22 | British Bio Technology | Synthetic gene for human granulocyte/macrophage colony stimulating factor. |
| WO1989010403A1 (en) * | 1988-04-21 | 1989-11-02 | Medvet Science Pty. Ltd. | Human gm-csf variants |
| US5109119A (en) * | 1989-06-06 | 1992-04-28 | Schering Corporation | Crystalline r-h-gm-csf and method |
| KR100448021B1 (ko) * | 2001-12-28 | 2004-09-08 | 크레아젠 주식회사 | 마우스 과립구 대식세포 콜로니 촉진인자 발현벡터 pGM-CSF로 형질전환된 대장균 및 상기 마우스 과립구 대식세포 콜로니 촉진인자의 대량생산방법 |
| CA2497554A1 (en) * | 2002-09-20 | 2004-04-01 | Dendreon Corporation | Immunotherapeutic compositions and methods for the treatment of moderately to well-differentiated cancers |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4438032A (en) * | 1981-01-30 | 1984-03-20 | The Regents Of The University Of California | Unique T-lymphocyte line and products derived therefrom |
| AU594014B2 (en) * | 1984-03-21 | 1990-03-01 | Research Corporation Technologies, Inc. | Recombinant DNA molecules |
| NZ212645A (en) * | 1984-07-06 | 1990-02-26 | Sandoz Ltd | Method for producing primate granulocyte-macrophage colony stimulating factor (gm-csf) |
| AU588819B2 (en) * | 1984-10-29 | 1989-09-28 | Immunex Corporation | Cloning of human granulocyte-macrophage colony stimulating factor gene |
| ZA856108B (en) * | 1984-10-29 | 1986-10-29 | Immunex Corp | Cloning of human granulocyte-macrophage colony simulating factor gene |
-
1985
- 1985-11-18 EP EP85906001A patent/EP0202300B1/de not_active Expired - Lifetime
- 1985-11-18 CN CN85109132D patent/CN1020473C/zh not_active Expired - Lifetime
- 1985-11-18 ZA ZA858833A patent/ZA858833B/xx unknown
- 1985-11-18 CN CN85109132A patent/CN1031465C/zh not_active Expired - Lifetime
- 1985-11-18 AU AU51963/86A patent/AU608741B2/en not_active Ceased
- 1985-11-18 KR KR1019860700480A patent/KR920003822B1/ko not_active Expired
- 1985-11-18 DE DE8585906001T patent/DE3586826T2/de not_active Expired - Lifetime
- 1985-11-18 ES ES548998A patent/ES8705470A1/es not_active Expired
- 1985-11-18 NZ NZ214225A patent/NZ214225A/xx unknown
- 1985-11-18 WO PCT/US1985/002250 patent/WO1986003225A1/en not_active Ceased
- 1985-11-18 IE IE288985A patent/IE59581B1/en not_active IP Right Cessation
- 1985-11-18 IL IL77080A patent/IL77080A/en not_active IP Right Cessation
- 1985-11-18 PT PT81513A patent/PT81513B/pt unknown
- 1985-11-18 JP JP60505271A patent/JP3038348B2/ja not_active Expired - Lifetime
- 1985-11-18 AT AT85906001T patent/ATE82321T1/de active
- 1985-11-18 HU HU86429A patent/HU213226B/hu unknown
- 1985-11-19 GR GR852786A patent/GR852786B/el unknown
-
1986
- 1986-06-24 FI FI862674A patent/FI103986B/fi not_active IP Right Cessation
- 1986-07-18 OA OA58906A patent/OA08671A/xx unknown
- 1986-07-18 NO NO862903A patent/NO862903L/no unknown
- 1986-07-21 DK DK198603452A patent/DK174598B1/da not_active IP Right Cessation
-
1987
- 1987-08-10 MY MYPI87001248A patent/MY101971A/en unknown
-
1992
- 1992-06-25 MX MX9203397A patent/MX9203397A/es unknown
-
1993
- 1993-01-16 CN CN93101072A patent/CN1045539C/zh not_active Expired - Lifetime
- 1993-06-30 NL NL930120C patent/NL930120I2/nl unknown
- 1993-07-01 LU LU88360C patent/LU88360I2/fr unknown
-
1994
- 1994-02-24 BG BG098563A patent/BG60840B2/bg unknown
-
1996
- 1996-01-11 HK HK6096A patent/HK6096A/en not_active IP Right Cessation
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PF | Patent in force | ||
| PE | Patent expired |
Effective date: 20051117 |