Compositions and methods that inhibit il-23 signaling
US-2024425579-A1 · Dec 26, 2024 · US
US9714287B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9714287-B2 |
| Application number | US-201615337512-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 28, 2016 |
| Priority date | Jun 30, 2005 |
| Publication date | Jul 25, 2017 |
| Grant date | Jul 25, 2017 |
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An anti-IL-23 antibody, including isolated nucleic acids that encode at least one anti-IL-23 antibody, vectors, host cells, transgenic animals or plants, and methods of making and using thereof have applications in diagnostic and/or therapeutic compositions, methods and devices.
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What is claimed is: 1. An isolated IL-23p19 antibody fragment, comprising a light chain variable region comprising: a complementarity determining region light chain 1 (CDRL1) amino acid sequence of SEQ ID NO:19; a CDRL2 amino acid sequence of SEQ ID NO:20; and a CDRL3 amino acid sequence of SEQ ID NO:21, and/or a heavy chain variable region comprising: a complementarity determining region heavy chain 1 (CDRH1) amino acid sequence of SEQ ID NO:14; a CDRH2 amino acid sequence of SEQ ID NO:15; and a CDRH3 amino acid sequence of SEQ ID NO:16. 2. The isolated IL-23p19 antibody fragment of claim 1 , comprising a light chain variable region amino acid sequence of SEQ ID NO:18. 3. The isolated IL-23p19 antibody fragment of claim 1 , comprising a heavy chain variable region amino acid sequence of SEQ ID NO:13. 4. The isolated IL-23p19 antibody fragment of claim 1 , wherein said antibody light chain variable region is at least one of chimerized, humanized, and CDR-grafted. 5. A composition comprising the isolated IL-23p19 antibody fragment of claim 1 , and at least one pharmaceutically acceptable carrier or diluent. 6. The composition of claim 5 , further comprising at least one compound or polypeptide selected from a detectable label or reporter, a TNF antagonist, an anti-infective drug, a cardiovascular (CV) system drug, a central nervous system (CNS) drug, an autonomic nervous system (ANS) drug, a respiratory tract drug, a gastrointestinal (GI) tract drug, a hormonal drug, a drug for fluid or electrolyte balance, a hematologic drug, an antineoplastic, an immunomodulation drug, an opthalmic, otic or nasal drug, a topical drug, a nutritional drug, a cytokine, and a cytokine antagonist. 7. The isolated IL-23p19 antibody fragment of claim 1 , wherein said fragment is selected from the group consisting of a Fab, Fab′, F(ab′) 2 , pFc, Fd, Fv, scFv, and fragments thereof. 8. An antibody that competitively binds to IL-23p19 with the isolated IL-23p19 antibody fragment of claim 1 . 9. The isolated IL-23p19 antibody fragment of claim 1 , wherein said antibody fragment binds IL-23p19 with at least one affinity selected from at least 10 −9 M, at least 10 −10 M, at least 10 −11 M, and at least 10 −12 M, at least 10 −13 M, at least 10 −14 M, and at least 10 −15 M, as determined by surface plasmon resonance or the Kinexa method. 10. The isolated IL-23p19 antibody fragment of claim 1 , wherein said antibody fragment binds IL-23p19 with an affinity between about 3.38×10 −10 M and about 4.3×10 −11 M, as determined by surface plasmon resonance. 11. The isolated IL-23-p19 antibody fragment of claim 1 , wherein said antibody fragment downregulates an activity of the IL-23 polypeptide comprising SEQ ID NO:1, the activity being selected from the group consisting of binding to the IL-23 receptor (IL-23R), induction of STAT3 phosphorylation, and IL-17 production.
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