WO2009073805A3 - Aglycosylated therapeutic antibodies and therapeutic antibody-encoding nucleotide sequences - Google Patents
Aglycosylated therapeutic antibodies and therapeutic antibody-encoding nucleotide sequences Download PDFInfo
- Publication number
- WO2009073805A3 WO2009073805A3 PCT/US2008/085568 US2008085568W WO2009073805A3 WO 2009073805 A3 WO2009073805 A3 WO 2009073805A3 US 2008085568 W US2008085568 W US 2008085568W WO 2009073805 A3 WO2009073805 A3 WO 2009073805A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- therapeutic
- aglycosylated
- nucleotide sequences
- encoding nucleotide
- antibodies
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
- C07K16/241—Tumor Necrosis Factors
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/40—Immunoglobulins specific features characterized by post-translational modification
- C07K2317/41—Glycosylation, sialylation, or fucosylation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/71—Decreased effector function due to an Fc-modification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
- C07K2317/734—Complement-dependent cytotoxicity [CDC]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
Provided are therapeutic polypeptides such as antibodies with reduced glycosylation and methods of designing and synthesizing the same. The therapeutic polypeptides can have reduced effector functions, and also can have additional advantages including, but not limited to, more efficient expression, purification, and improved patient response. In some embodiments, the polypeptide is a recombinantly- produced humanized antibody targeting a cytokine with specificity for a particular cytokine relative to other naturally-occurring human antigens, wherein the antibody has a constant region, and wherein the constant region is aglycosylated.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US99229107P | 2007-12-04 | 2007-12-04 | |
| US60/992,291 | 2007-12-04 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2009073805A2 WO2009073805A2 (en) | 2009-06-11 |
| WO2009073805A3 true WO2009073805A3 (en) | 2009-07-30 |
Family
ID=40627568
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2008/085568 Ceased WO2009073805A2 (en) | 2007-12-04 | 2008-12-04 | Aglycosylated therapeutic antibodies and therapeutic antibody-encoding nucleotide sequences |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2009073805A2 (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2011201157C1 (en) * | 2002-12-24 | 2017-09-07 | Rinat Neuroscience Corp. | Anti-NGF antibodies and methods using same |
| GB201000588D0 (en) * | 2010-01-14 | 2010-03-03 | Ucb Pharma Sa | Bacterial host strain |
| EP2546267A1 (en) * | 2011-07-13 | 2013-01-16 | UCB Pharma S.A. | Bacterial host strain expressing recombinant DsbC |
| GB201112429D0 (en) * | 2011-07-19 | 2011-08-31 | Glaxo Group Ltd | Antigen-binding proteins with increased FcRn binding |
| MX2015003007A (en) | 2012-09-07 | 2015-06-05 | Coherus Biosciences Inc | Stable aqueous formulations of adalimumab. |
| CN103446583B (en) * | 2013-03-21 | 2015-11-18 | 百奥泰生物科技(广州)有限公司 | A kind of people's antibody preparation for the treatment of TNF-alpha associated disorders |
| US10376582B2 (en) * | 2013-10-16 | 2019-08-13 | Outlook Therapeutics, Inc. | Buffer formulations for enhanced antibody stability |
| WO2016118707A1 (en) | 2015-01-21 | 2016-07-28 | Oncobiologics, Inc. | Modulation of charge variants in a monoclonal antibody composition |
| US11229702B1 (en) | 2015-10-28 | 2022-01-25 | Coherus Biosciences, Inc. | High concentration formulations of adalimumab |
| AU2017213775A1 (en) * | 2016-02-03 | 2018-08-16 | Outlook Therapeutics, Inc. | Buffer formulations for enhanced antibody stability |
| WO2017184880A1 (en) | 2016-04-20 | 2017-10-26 | Coherus Biosciences, Inc. | A method of filling a container with no headspace |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5082767A (en) * | 1989-02-27 | 1992-01-21 | Hatfield G Wesley | Codon pair utilization |
| US6090382A (en) * | 1996-02-09 | 2000-07-18 | Basf Aktiengesellschaft | Human antibodies that bind human TNFα |
| US6979556B2 (en) * | 2000-12-14 | 2005-12-27 | Genentech, Inc. | Separate-cistron contructs for secretion of aglycosylated antibodies from prokaryotes |
| WO2007014162A2 (en) * | 2005-07-21 | 2007-02-01 | Abbott Laboratories | Multiple gene expression including sorf constructs and methods with polyproteins, pro-proteins, and proteolysis |
-
2008
- 2008-12-04 WO PCT/US2008/085568 patent/WO2009073805A2/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5082767A (en) * | 1989-02-27 | 1992-01-21 | Hatfield G Wesley | Codon pair utilization |
| US6090382A (en) * | 1996-02-09 | 2000-07-18 | Basf Aktiengesellschaft | Human antibodies that bind human TNFα |
| US6979556B2 (en) * | 2000-12-14 | 2005-12-27 | Genentech, Inc. | Separate-cistron contructs for secretion of aglycosylated antibodies from prokaryotes |
| WO2007014162A2 (en) * | 2005-07-21 | 2007-02-01 | Abbott Laboratories | Multiple gene expression including sorf constructs and methods with polyproteins, pro-proteins, and proteolysis |
Non-Patent Citations (4)
| Title |
|---|
| ANDERSEN D C ET AL: "Production technologies for monoclonal antibodies and their fragments", CURRENT OPINION IN BIOTECHNOLOGY, LONDON, GB, vol. 15, no. 5, 1 October 2004 (2004-10-01), pages 456 - 462, XP004588033, ISSN: 0958-1669 * |
| MAZOR YARIV ET AL: "Isolation of engineered, full-length antibodies from libraries expressed in Escherichia coli", NATURE BIOTECHNOLOGY, NATURE PUBLISHING GROUP, NEW YORK, NY, US, vol. 25, no. 5, 1 May 2007 (2007-05-01), pages 563 - 565, XP002488027, ISSN: 1087-0156, [retrieved on 20070415] * |
| SIMMONS L C ET AL: "Expression of full-length immunoglobulins in Escherichia coli: rapid and efficient production of aglycosylated antibodies", JOURNAL OF IMMUNOLOGICAL METHODS, ELSEVIER SCIENCE PUBLISHERS B.V.,AMSTERDAM, NL, vol. 263, no. 1-2, 1 May 2002 (2002-05-01), pages 133 - 147, XP004354391, ISSN: 0022-1759 * |
| STEINER DANIEL ET AL: "Signal sequences directing cotranslational translocation expand the range of proteins amenable to phage display", NATURE BIOTECHNOLOGY, vol. 24, no. 7, July 2006 (2006-07-01), pages 823 - 831, XP009117243, ISSN: 1087-0156 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009073805A2 (en) | 2009-06-11 |
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