Optimized Fc variants

US9663582B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9663582-B2
Application numberUS-201414326373-A
CountryUS
Kind codeB2
Filing dateJul 8, 2014
Priority dateMar 3, 2003
Publication dateMay 30, 2017
Grant dateMay 30, 2017

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present invention relates to Fc variants having decreased affinity for FcγRIIb, methods for their generation, Fc polypeptides comprising optimized Fc variants, and methods for using optimized Fc variants.

First claim

Opening claim text (preview).

We claim: 1. A nucleic acid encoding a protein, wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an amino acid substitution selected from the group consisting of S267E and S267D in the Fc region, wherein said Fc variant exhibits increased binding to FcγRIIb as compared to the parent IgG Fc polypeptide and wherein numbering is according to the EU index. 2. The nucleic acid according to claim 1 , wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267E amino acid substitution in the Fc region. 3. An expression vector comprising the nucleic of claim 2 . 4. The nucleic acid according to claim 1 , wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267D amino acid substitution in the Fc region. 5. An expression vector comprising the nucleic of claim 4 . 6. The nucleic acid according to 1 , wherein said parent IgG Fc polypeptide is a human IgG1. 7. A host cell comprising a nucleic acid encoding a protein, wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an amino acid substitution selected from the group consisting of S267E and S267D in the Fc region, wherein said Fc variant exhibits increased binding to FcγRIIb as compared to the parent IgG Fc polypeptide and wherein numbering is according to the EU index. 8. The host cell according to claim 7 , wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267E amino acid substitution in the Fc region. 9. The host cell according to claim 7 , wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267D amino acid substitution in the Fc region. 10. The host cell according to claim 7 , comprising a nucleic acid encoding a protein, wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267E amino acid substitution in the Fc region. 11. The host cell according to claim 7 , comprising an expression vector comprising a nucleic acid encoding a protein, wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267E amino acid substitution in the Fc region. 12. The host cell according to claim 7 , comprising a nucleic acid encoding a protein, wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267D amino acid substitution in the Fc region. 13. The host cell according to claim 7 , comprising an expression vector comprising a nucleic acid encoding a protein, wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267D amino acid substitution in the Fc region. 14. The host cell according to claim 12 or 13 , wherein said protein is an antibody or Fc fusion. 15. The host cell according to claim 14 , wherein said protein is an antibody. 16. The host cell according to claim 14 , wherein said protein is an Fc fusion. 17. The host cell according to claim 15 , wherein said antibody is selected from the group consisting of a human antibody, a humanized antibody, and a chimeric antibody. 18. The host cell according to claim 17 , wherein said antibody is a humanized antibody. 19. The host cell according to claim 17 , wherein said antibody is a chimeric antibody. 20. The host cell according to claim 7 , wherein said parent IgG Fc polypeptide is a human IgG1. 21. A method of making a protein comprising: a) culturing a host cell comprising a nucleic acid encoding a protein, wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an amino acid substitution selected from the group consisting of S267E and S267D in the Fc region, wherein said Fc variant exhibits increased binding to FcγRIIb as compared to the parent IgG Fc polypeptide and wherein numbering is according to the EU index, under conditions wherein said protein is produced; and b) purifying said protein. 22. The method of making according to claim 21 , wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267E amino acid substitution in the Fc region. 23. The method of making according to claim 21 , wherein said protein comprises an Fc variant of a parent IgG Fc polypeptide, said Fc variant comprising an S267D amino acid substitution in the Fc region. 24. The method of making according to claim 22 or 23 , wherein said protein is an antibody or Fc fusion. 25. The method of making according to claim 24 , wherein said protein is an antibody. 26. The method of making according to claim 24 , wherein said protein is an Fc fusion. 27. The method of making a protein according to claim 25 , wherein said antibody is selected from the group consisting of a human antibody, a humanized antibody, and a chimeric antibody. 28. The method of making according to claim 27 , wherein said antibody is a humanized antibody. 29. The method of making according to claim 27 , wherein said antibody is a chimeric antibody. 30. The method of making according to claim 21 , wherein said parent IgG Fc polypeptide is a human IgG1.

Assignees

Inventors

Classifications

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • from tumour cells · CPC title

  • comprising antibodies · CPC title

  • Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies · CPC title

  • against molecules with a "CD"-designation, not provided for elsewhere · CPC title

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What does patent US9663582B2 cover?
The present invention relates to Fc variants having decreased affinity for FcγRIIb, methods for their generation, Fc polypeptides comprising optimized Fc variants, and methods for using optimized Fc variants.
Who is the assignee on this patent?
Xencor Inc
What technology area does this patent fall under?
Primary CPC classification C07K16/2893. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).