Compositions and methods that inhibit il-23 signaling
US-2024425579-A1 · Dec 26, 2024 · US
US10259867B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10259867-B2 |
| Application number | US-201715583487-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 1, 2017 |
| Priority date | Aug 7, 2000 |
| Publication date | Apr 16, 2019 |
| Grant date | Apr 16, 2019 |
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Isolated anti-IL-12 antibodies, nucleic acids encoding antibodies or antibody portions, vectors, host cells, and methods of making are useful for production of antibody or portions for treating and/or diagnosing IL-12 related conditions, diseases, and disorders, such as psoriasis.
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What is claimed is: 1. A method for reducing symptoms of systemic lupus erythematosus in an animal, comprising administering a composition comprising an effective amount of an isolated anti-IL-12 antibody comprising a heavy chain variable region of the amino acid sequence of SEQ ID NO: 7 and a light chain variable region of the amino acid sequence of SEQ ID NO: 8, to said animal. 2. The method according to claim 1 , wherein said effective amount is 0.001-50 mg/kilogram of said animal. 3. The method according to claim 1 , wherein said administering is subcutaneous. 4. The method according to claim 1 , further comprising administering at least one composition comprising an effective amount of a cytokine antagonist. 5. A method for reducing symptoms of systemic lupus erythematosus in an animal, comprising administering a composition comprising an effective amount of an isolated anti-IL-12 antibody comprising a heavy chain complementarity determining region CDR 1 of the amino acid sequence of SEQ ID NO: 1, a heavy chain CDR2 of the amino acid sequence of SEQ ID NO: 2, a heavy chain CDR3 of the amino acid sequence of SEQ ID NO: 3, a light chain CDR1 of the amino acid sequence of SEQ ID NO: 4, a light chain CDR2 of the amino acid sequence of SEQ ID NO: 5, and a light chain CDR3 of the amino acid sequence of SEQ ID NO: 6, to said animal. 6. The method according to claim 5 , wherein said effective amount is 0.001-50 mg/kilogram of said animal. 7. The method according to claim 5 , wherein said administering is subcutaneous. 8. The method according to claim 5 , further comprising administering at least one composition comprising an effective amount of a cytokine antagonist. 9. A method for reducing symptoms of systemic lupus erythematosus in a human, comprising administering a composition comprising an effective amount of an isolated anti-IL-12 antibody comprising a heavy chain variable region of the amino acid sequence of SEQ ID NO: 7 and a light chain variable region of the amino acid sequence of SEQ ID NO: 8, to said human. 10. The method according to claim 9 , wherein said effective amount is 0.001-50 mg/kilogram of said human. 11. The method according to claim 9 , wherein said administering is subcutaneous. 12. The method according to claim 9 , further comprising administering at least one composition comprising an effective amount of a cytokine antagonist. 13. A method for reducing symptoms of systemic lupus erythematosus in a human, comprising administering a composition comprising an effective amount of an isolated anti-IL-12 antibody comprising a heavy chain complementarity determining region CDR 1 of the amino acid sequence of SEQ ID NO: 1, a heavy chain CDR2 of the amino acid sequence of SEQ ID NO: 2, a heavy chain CDR3 of the amino acid sequence of SEQ ID NO: 3, a light chain CDR1 of the amino acid sequence of SEQ ID NO: 4, a light chain CDR2 of the amino acid sequence of SEQ ID NO: 5, and a light chain CDR3 of the amino acid sequence of SEQ ID NO: 6, to said human. 14. The method according to claim 13 , wherein said effective amount is 0.001-50 mg/kilogram of said human. 15. The method according to claim 13 , wherein said administering is subcutaneous. 16. The method according to claim 13 , further comprising administering at least one composition comprising an effective amount of a cytokine antagonist.
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