Crispr/cas-related methods and compositions for knocking out c5
US-2024415980-A1 · Dec 19, 2024 · US
US9309306B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9309306-B2 |
| Application number | US-201213590904-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 21, 2012 |
| Priority date | Aug 23, 2011 |
| Publication date | Apr 12, 2016 |
| Grant date | Apr 12, 2016 |
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The invention provides anti-MCSP antibodies and methods of using the same.
Opening claim text (preview).
What is claimed is: 1. An isolated antibody that binds to human Melanoma chondroitin sulfate proteoglycan (MCSP) wherein the antibody comprises (a) HVR-H1 comprising the amino acid sequence of SEQ ID NO: 17; (b) HVR-H2 comprising the amino acid sequence of SEQ ID NO: 18; and (c) HVR-H3 comprising the amino acid sequence of SEQ ID NO: 16. 2. The antibody of claim 1 , further comprising (a) HVR-L1 comprising the amino acid sequence of SEQ ID NO: 13; (b) HVR-L2 comprising the amino acid sequence of SEQ ID NO: 11; and (c) HVR-L3 comprising the amino acid sequence of SEQ ID NO: 12. 3. An isolated antibody that binds to human Melanoma chondroitin sulfate proteoglycan (MCSP), wherein the antibody comprises (a) HVR-L1 comprising the amino acid sequence of SEQ ID NO:13; (b) HVR-L2 comprising the amino acid sequence of SEQ ID NO: 11; and (c) HVR-L3 comprising the amino acid sequence of SEQ ID NO: 12. 4. The antibody of claim 2 , comprising (a) a VH sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 32; (b) a VL sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 31; or (c) a VH sequence as in (a) and a VL sequence as in (b). 5. The antibody of claim 4 , comprising a VH sequence of SEQ ID NO: 32. 6. The antibody of claim 4 , comprising a VL sequence of SEQ ID NO: 31. 7. The antibody of claim 4 , comprising a VH sequence of SEQ ID NO: 32 and a VL sequence of SEQ ID NO: 31. 8. An immunoconjugate comprising the antibody of claim 2 and a cytotoxic agent. 9. A pharmaceutical formulation comprising the antibody of claim 2 and a pharmaceutically acceptable carrier. 10. The antibody of claim 2 , wherein the antibody is a monoclonal, humanized, or chimeric antibody. 11. The antibody of claim 2 , wherein the antibody is a full-length IgG class antibody. 12. The antibody of claim 11 , wherein the antibody has been glycoengineered to modify the oligosaccharides in the Fc region and wherein the antibody has increased ADCC effector function as compared to an non-glycoengineered antibody. 13. The antibody of claim 12 , wherein the Fc region has a reduced number of fucose residues as compared to the nonglycoengineered antibody. 14. The antibody of claim 12 , wherein the antibody has an increased ratio of GlcNAc residues to fucose residues in the Fc region compared to the non-glycoengineered antibody. 15. The antibody of claim 12 , wherein the Fc region has an increased proportion of bisected oligosaccharides as compared to the non-glycoengineered antibody. 16. The antibody of claim 7 , wherein the antibody is a monoclonal, humanized, or chimeric antibody. 17. The antibody of claim 7 , wherein the antibody is a full-length IgG class antibody. 18. The antibody of claim 17 , wherein the antibody has been glycoengineered to modify the oligosaccharides in the Fc region and wherein the antibody has increased ADCC effector function as compared to an non-glycoengineered antibody. 19. The antibody of claim 18 , wherein the Fc region has a reduced number of fucose residues as compared to the nonglycoengineered antibody. 20. The antibody of claim 18 , wherein the antibody has an increased ratio of GlcNAc residues to fucose residues in the Fc region compared to the non-glycoengineered antibody. 21. The antibody of claim 18 , wherein the Fc region has an increased proportion of bisected oligosaccharides as compared to the non-glycoengineered antibody.
comprising antibodies · CPC title
containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title
against material from animals or humans · CPC title
Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity · CPC title
specific for leukemia · CPC title
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