CS215108B2 - Method of making the interferrone - Google Patents
Method of making the interferrone Download PDFInfo
- Publication number
- CS215108B2 CS215108B2 CS784645A CS464578A CS215108B2 CS 215108 B2 CS215108 B2 CS 215108B2 CS 784645 A CS784645 A CS 784645A CS 464578 A CS464578 A CS 464578A CS 215108 B2 CS215108 B2 CS 215108B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- cells
- interferon
- concentration
- acid
- sodium
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 16
- 102000014150 Interferons Human genes 0.000 claims abstract description 86
- 108010050904 Interferons Proteins 0.000 claims abstract description 86
- 229940079322 interferon Drugs 0.000 claims abstract description 83
- 150000003839 salts Chemical class 0.000 claims abstract description 12
- 241000700605 Viruses Species 0.000 claims abstract description 11
- 231100000252 nontoxic Toxicity 0.000 claims abstract description 3
- 230000003000 nontoxic effect Effects 0.000 claims abstract description 3
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 30
- 239000002609 medium Substances 0.000 claims description 23
- 239000002253 acid Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 13
- 239000011734 sodium Substances 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 239000001963 growth medium Substances 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 230000016396 cytokine production Effects 0.000 claims description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 230000001939 inductive effect Effects 0.000 claims description 4
- 239000011591 potassium Substances 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 238000012258 culturing Methods 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 8
- 230000006698 induction Effects 0.000 abstract description 6
- 206010028980 Neoplasm Diseases 0.000 abstract description 5
- 201000011510 cancer Diseases 0.000 abstract description 4
- 239000000411 inducer Substances 0.000 abstract description 3
- 230000000840 anti-viral effect Effects 0.000 abstract description 2
- 238000004113 cell culture Methods 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 description 134
- 210000002966 serum Anatomy 0.000 description 15
- 244000309466 calf Species 0.000 description 11
- 239000006285 cell suspension Substances 0.000 description 11
- MFBOGIVSZKQAPD-UHFFFAOYSA-M sodium butyrate Chemical compound [Na+].CCCC([O-])=O MFBOGIVSZKQAPD-UHFFFAOYSA-M 0.000 description 8
- 241000711408 Murine respirovirus Species 0.000 description 7
- 239000012737 fresh medium Substances 0.000 description 7
- 239000000725 suspension Substances 0.000 description 6
- SWEYNHYBJHPVJL-UHFFFAOYSA-N butanoic acid;sodium Chemical compound [Na].CCCC(O)=O SWEYNHYBJHPVJL-UHFFFAOYSA-N 0.000 description 5
- 210000000265 leukocyte Anatomy 0.000 description 5
- 241000701044 Human gammaherpesvirus 4 Species 0.000 description 4
- 239000012980 RPMI-1640 medium Substances 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 235000015097 nutrients Nutrition 0.000 description 4
- 239000006228 supernatant Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- 210000002950 fibroblast Anatomy 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 229940047124 interferons Drugs 0.000 description 3
- 239000008363 phosphate buffer Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000711404 Avian avulavirus 1 Species 0.000 description 2
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 2
- 229920002307 Dextran Polymers 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 241000282412 Homo Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000710961 Semliki Forest virus Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000003443 antiviral agent Substances 0.000 description 2
- 150000004652 butanoic acids Chemical class 0.000 description 2
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 2
- 210000004700 fetal blood Anatomy 0.000 description 2
- 239000012894 fetal calf serum Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000035931 haemagglutination Effects 0.000 description 2
- 210000005260 human cell Anatomy 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 210000003292 kidney cell Anatomy 0.000 description 2
- 239000002953 phosphate buffered saline Substances 0.000 description 2
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- LHYPLJGBYPAQAK-UHFFFAOYSA-M sodium;pentanoate Chemical compound [Na+].CCCCC([O-])=O LHYPLJGBYPAQAK-UHFFFAOYSA-M 0.000 description 2
- 230000000638 stimulation Effects 0.000 description 2
- FGMPLJWBKKVCDB-BYPYZUCNSA-N (2s)-1-hydroxypyrrolidine-2-carboxylic acid Chemical compound ON1CCC[C@H]1C(O)=O FGMPLJWBKKVCDB-BYPYZUCNSA-N 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 108010024636 Glutathione Proteins 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 102000006992 Interferon-alpha Human genes 0.000 description 1
- 108010047761 Interferon-alpha Proteins 0.000 description 1
- 150000008575 L-amino acids Chemical class 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- 206010025323 Lymphomas Diseases 0.000 description 1
- 206010028470 Mycoplasma infections Diseases 0.000 description 1
- 229930193140 Neomycin Natural products 0.000 description 1
- 206010035226 Plasma cell myeloma Diseases 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- -1 Sodium butyric acid sodium chloride Chemical compound 0.000 description 1
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- UYXTWWCETRIEDR-UHFFFAOYSA-N Tributyrin Chemical compound CCCC(=O)OCC(OC(=O)CCC)COC(=O)CCC UYXTWWCETRIEDR-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 229960001230 asparagine Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- ICSSIKVYVJQJND-UHFFFAOYSA-N calcium nitrate tetrahydrate Chemical compound O.O.O.O.[Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ICSSIKVYVJQJND-UHFFFAOYSA-N 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 230000007541 cellular toxicity Effects 0.000 description 1
- 230000000973 chemotherapeutic effect Effects 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000012228 culture supernatant Substances 0.000 description 1
- 210000004544 dc2 Anatomy 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- PYLIXCKOHOHGKQ-UHFFFAOYSA-L disodium;hydrogen phosphate;heptahydrate Chemical compound O.O.O.O.O.O.O.[Na+].[Na+].OP([O-])([O-])=O PYLIXCKOHOHGKQ-UHFFFAOYSA-L 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 201000006747 infectious mononucleosis Diseases 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229960005337 lysine hydrochloride Drugs 0.000 description 1
- WRUGWIBCXHJTDG-UHFFFAOYSA-L magnesium sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Mg+2].[O-]S([O-])(=O)=O WRUGWIBCXHJTDG-UHFFFAOYSA-L 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
- 201000000050 myeloid neoplasm Diseases 0.000 description 1
- 229960004927 neomycin Drugs 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 210000005259 peripheral blood Anatomy 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 230000007505 plaque formation Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000008160 pyridoxine Nutrition 0.000 description 1
- 239000011677 pyridoxine Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- UDWXLZLRRVQONG-UHFFFAOYSA-M sodium hexanoate Chemical compound [Na+].CCCCCC([O-])=O UDWXLZLRRVQONG-UHFFFAOYSA-M 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- 239000004324 sodium propionate Substances 0.000 description 1
- 229960003212 sodium propionate Drugs 0.000 description 1
- 235000010334 sodium propionate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- 235000019157 thiamine Nutrition 0.000 description 1
- 239000011721 thiamine Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
- 230000029812 viral genome replication Effects 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
Classifications
-
- 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
- C07K14/555—Interferons [IFN]
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2987177 | 1977-07-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CS215108B2 true CS215108B2 (en) | 1982-07-30 |
Family
ID=10298554
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CS784645A CS215108B2 (en) | 1977-07-15 | 1978-07-11 | Method of making the interferrone |
Country Status (15)
Country | Link |
---|---|
US (1) | US4216203A (it) |
EP (1) | EP0000520B1 (it) |
JP (1) | JPS5420119A (it) |
AT (1) | AT362334B (it) |
AU (1) | AU524099B2 (it) |
CA (1) | CA1115209A (it) |
CS (1) | CS215108B2 (it) |
DE (1) | DE2860559D1 (it) |
DK (1) | DK147625C (it) |
ES (1) | ES471721A1 (it) |
FI (1) | FI60971C (it) |
HU (1) | HU179655B (it) |
IL (1) | IL55143A0 (it) |
IT (1) | IT1107573B (it) |
PL (1) | PL110704B1 (it) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0005476B1 (de) * | 1978-05-17 | 1981-12-30 | Dr. Karl Thomae GmbH | Verfahren zur Herstellung von Humaninterferon |
JPS55122717A (en) * | 1979-03-15 | 1980-09-20 | Asai Gerumaniumu Kenkyusho:Kk | Interferon inducer |
DE2946275A1 (de) * | 1979-11-16 | 1981-05-27 | Dr. Karl Thomae Gmbh, 7950 Biberach | Verbessertes verfahren zur herstellung von humaninterferon aus lymphoblastoiden zellen |
JPS56135420A (en) * | 1980-03-26 | 1981-10-22 | Fumiaki Taguchi | Suppressive substance of virus and its preparation |
ATE56471T1 (de) | 1980-04-03 | 1990-09-15 | Biogen Inc | Dns-sequenzen, rekombinante dns-molekuele und verfahren zur herstellung von dem menschlichen fibroblast-interferon. |
US4460574A (en) * | 1980-06-16 | 1984-07-17 | Yabrov Alexander A | Prophylaxis or treatment of interferon-sensitive diseases |
JPS5754586A (en) * | 1980-09-18 | 1982-04-01 | Ajinomoto Co Inc | Cell strain producing human interferon prolongably, its preparation, and preparation of human interferon using it |
FR2502009A1 (fr) * | 1981-03-23 | 1982-09-24 | Centre Nat Rech Scient | Perfectionnements aux procedes de fabrication d'interferon |
EP0062085B1 (de) * | 1981-04-07 | 1985-08-14 | Dr. Karl Thomae GmbH | Verbessertes Verfahren zur Herstellung von Humaninterferon aus lymphoblastoiden Zellen |
HU184972B (en) * | 1981-12-01 | 1984-11-28 | Egyt Gyogyszervegyeszeti Gyar | Process for preparing human gamma interferone |
CS251766B2 (en) * | 1982-06-21 | 1987-08-13 | Wellcome Found | Method of interferon production |
US4745053A (en) * | 1983-07-08 | 1988-05-17 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyojo | Process for producing human interferon and method for assaying the interferon productivity of blood |
US4956282A (en) * | 1985-07-29 | 1990-09-11 | Calgene, Inc. | Mammalian peptide expression in plant cells |
US6774283B1 (en) | 1985-07-29 | 2004-08-10 | Calgene Llc | Molecular farming |
DE3930140A1 (de) * | 1989-09-09 | 1991-03-21 | Bayer Ag | Verfahren zur herstellung von biologischen materialien in zellkulturen und vorrichtungen |
US5378612A (en) * | 1990-05-11 | 1995-01-03 | Juridical Foundation The Chemo-Sero-Therapeutic Research Institute | Culture medium for production of recombinant protein |
JPH0775593A (ja) * | 1993-09-08 | 1995-03-20 | Suntory Ltd | 蛋白質の製造方法 |
WO1997007820A1 (fr) * | 1995-08-30 | 1997-03-06 | Toray Industries, Inc. | Remede destine aux maladies cardiaques |
US6833271B2 (en) * | 1996-12-04 | 2004-12-21 | Medi-Cult A/S | Serum-free cell culture media |
SE513313C2 (sv) | 1998-12-29 | 2000-08-21 | Bionative Ab | Modifierad interferonproduktion |
US7294481B1 (en) * | 1999-01-05 | 2007-11-13 | Immunex Corporation | Method for producing recombinant proteins |
GB0208041D0 (en) * | 2002-04-08 | 2002-05-22 | Lonza Biologics Plc | Method of culturing animal cells |
WO2019229929A1 (ja) | 2018-05-31 | 2019-12-05 | 東芝キヤリア株式会社 | タッチパネルを用いた設備管理装置および管理画面生成方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1464939A (en) * | 1974-01-11 | 1977-02-16 | Anvar | Process for the production of interferon |
FR2282910A2 (fr) | 1974-08-26 | 1976-03-26 | Anvar | Procede de fabrication a l'echelle industrielle de preparations d'interferon de titre eleve |
-
1978
- 1978-07-11 CS CS784645A patent/CS215108B2/cs unknown
- 1978-07-14 DE DE7878100395T patent/DE2860559D1/de not_active Expired
- 1978-07-14 US US05/924,703 patent/US4216203A/en not_active Expired - Lifetime
- 1978-07-14 AT AT510378A patent/AT362334B/de not_active IP Right Cessation
- 1978-07-14 IT IT50322/78A patent/IT1107573B/it active Protection Beyond IP Right Term
- 1978-07-14 JP JP8599878A patent/JPS5420119A/ja active Granted
- 1978-07-14 PL PL1978208407A patent/PL110704B1/pl unknown
- 1978-07-14 IL IL55143A patent/IL55143A0/xx not_active IP Right Cessation
- 1978-07-14 ES ES471721A patent/ES471721A1/es not_active Expired
- 1978-07-14 DK DK316978A patent/DK147625C/da not_active IP Right Cessation
- 1978-07-14 AU AU38049/78A patent/AU524099B2/en not_active Expired
- 1978-07-14 FI FI782249A patent/FI60971C/fi not_active IP Right Cessation
- 1978-07-14 CA CA307,456A patent/CA1115209A/en not_active Expired
- 1978-07-14 EP EP78100395A patent/EP0000520B1/en not_active Expired
- 1978-07-14 HU HU78WE579A patent/HU179655B/hu not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
PL110704B1 (en) | 1980-07-31 |
HU179655B (en) | 1982-11-29 |
JPS5646797B2 (it) | 1981-11-05 |
CA1115209A (en) | 1981-12-29 |
EP0000520A1 (en) | 1979-02-07 |
IL55143A0 (en) | 1978-09-29 |
JPS5420119A (en) | 1979-02-15 |
US4216203A (en) | 1980-08-05 |
FI782249A7 (fi) | 1979-01-16 |
FI60971B (fi) | 1982-01-29 |
ES471721A1 (es) | 1979-02-01 |
IT1107573B (it) | 1985-11-25 |
PL208407A1 (pl) | 1979-03-12 |
DK316978A (da) | 1979-01-16 |
AU524099B2 (en) | 1982-09-02 |
IT7850322A0 (it) | 1978-07-14 |
FI60971C (fi) | 1982-05-10 |
AU3804978A (en) | 1980-01-17 |
DK147625B (da) | 1984-10-22 |
DE2860559D1 (en) | 1981-04-16 |
ATA510378A (de) | 1980-10-15 |
DK147625C (da) | 1985-04-29 |
EP0000520B1 (en) | 1981-03-25 |
AT362334B (de) | 1981-05-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CS215108B2 (en) | Method of making the interferrone | |
PRASAD | Morphological differentiation induced by prostaglandin in mouse neuroblastoma cells in culture | |
CA1323564C (en) | Low dosage of interferon to enhance vaccine efficiency | |
US5518899A (en) | Preparation of human myelomonocyte interferon-gamma | |
AU6642390A (en) | Methods and compositions for promoting immunopotentiation | |
Wittmann et al. | Cell-mediated immunity in Aujeszky disease virus infected pigs: I. Lymphocyte stimulation | |
Furth | Recent experimental studies on leukemia | |
CS251766B2 (en) | Method of interferon production | |
EP0538330B1 (en) | Beta-alethine use in cell culture and therapy | |
NO173144B (no) | Fremgangsmaate til fremstilling av interferongamma | |
US4480032A (en) | Natural mixture of Type I and Type II interferons | |
SU1830080A3 (ru) | Бессыворотомная питательная среда для культуры ткани | |
US6245561B1 (en) | β-alethine use in cell culture and therapy | |
JP2926409B2 (ja) | 癌転移抑制因子の製造方法 | |
CHUDZIO et al. | SHORT COMMUNICATION Platelet-Derived Growth Factor (PDGF) Inhibits Priming in Synchronous Mouse or Human Fibroblasts Producing Interferon | |
CA2087883C (en) | Beta-alethine use in cell culture and therapy | |
SU1495374A1 (ru) | Штамм культивируемых клеток животных MUS мUSсULUS - продуцент ростстимулирующих факторов гибридом | |
JPS6293300A (ja) | インタ−フエロン組成物 | |
WO1988000236A1 (en) | Methods and materials for vanadium immunomodulation | |
EP0093375A1 (de) | Kulturmedium und Verfahren zur Virusvermehrung in Suspensionskultur | |
Negroni et al. | Antigenic heterogeneity in cell populations of cloned polyoma, virus-induced tumour lines | |
Cowdery, Jr et al. | T cell mediated polyclonal B cell activation induced by cell-bound fetal calf serum | |
Adams | Culture characteristics of brain neuroglial cells from chickens infected with Rous sarcoma virus | |
Miller et al. | Failure of Sulphanilamide to Inhibit Calcification of Bone | |
Wagle et al. | Studies on Amino Acid Incorporation into Protein of Tumors Induced by Rous Sarcoma Virus and Hyperplasia Induced by Fowl Pox Virus in Chorioallantoic Membrane of Chicken Embryos |