FC-REGION VARIANTS WITH MODIFIED FCRN-BINDING PROPERTIES

• US 20170037121A1
• Filed: 07/14/2016
• Published: 02/09/2017
• Est. Priority Date: 01/15/2014
• Status: Abandoned Application

• Current Assignee: Hoffmann-La Roche Incorporated (Roche Holding AG)
• Original Assignee: Hoffmann-La Roche Incorporated (Roche Holding AG)
• Inventors: Schlothauer, Tilman
• Application Number:
  US15/210,218
• Publication Number:
  US 20170037121A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61K 2039/505 comprising antibodies
• CPC Class Codes: A61P 27/02 Ophthalmic agents
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: C07K 16/22 against growth factors ; against growth regulators
• CPC Class Codes: C07K 2317/31 multispecific
• CPC Class Codes: C07K 2317/33 Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
• CPC Class Codes: C07K 2317/524 CH2 domain
• CPC Class Codes: C07K 2317/526 CH3 domain
• CPC Class Codes: C07K 2317/53 Hinge
• CPC Class Codes: C07K 2317/64 comprising a combination of variable region and constant region components
• CPC Class Codes: C07K 2317/92 Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
• CPC Class Codes: C07K 2317/94 Stability, e.g. half-life, pH, temperature or enzyme-resistance

Abstract

Herein is reported a polypeptide comprising a first polypeptide and a second polypeptide each comprising in N-terminal to C-terminal direction at least a portion of an immunoglobulin hinge region, which comprises one or more cysteine residues, an immunoglobulin CH2-domain and an immunoglobulin CH3-domain, wherein

• • i) the first and the second polypeptide comprise the mutations H310A, H433A and Y436A, or
  • ii) the first and the second polypeptide comprise the mutations L251D, L314D and L432D, or
  • iii) the first and the second polypeptide comprise the mutations L251S, L314S and L432S.

Claims

1. A polypeptide comprising

a first polypeptide and a second polypeptide each comprising in N-terminal to C-terminal direction at least a portion of an immunoglobulin hinge region, which comprises one or more cysteine residues, an immunoglobulin CH2-domain and an immunoglobulin CH3-domain,

wherein

i) the first and the second polypeptide comprise the mutations H310A, H433A and Y436A, or

ii) the first and the second polypeptide comprise the mutations L251D, L314D and L432D, or

iii) the first and the second polypeptide comprise the mutations L251S, L314S and L432S.

2. The polypeptide according to claim 1, wherein the polypeptide does not specifically bind to the human FcRn and does specifically bind to Staphylococcal protein A.

3. The polypeptide according to claim 1, wherein the polypeptide is a homodimeric polypeptide.

4. The polypeptide according to claim 1, wherein the polypeptide is a heterodimeric polypeptide.

5. The polypeptide according to claim 1, wherein i) the first polypeptide further comprises the mutations Y349C, T366S, L368A and Y407V and the second polypeptide comprises the mutations S354C and T366W, or ii) the first polypeptide comprises the mutations S354C, T366S, L368A and Y407V and the second polypeptide comprises the mutations Y349C and T366W.

6. The polypeptide according to claim 1, wherein the immunoglobulin hinge region, the immunoglobulin CH2-domain and the immunoglobulin CH3-domain are of the human IgG1 subclass.

7. The polypeptide according to claim 1, wherein the first polypeptide and the second polypeptide further comprise the mutations L234A and L235A.

8. The polypeptide according to claim 1, wherein the immunoglobulin hinge region, the immunoglobulin CH2-domain and the immunoglobulin CH3-domain are of the human IgG2 subclass.

9. The polypeptide according to claim 1, wherein the immunoglobulin hinge region, the immunoglobulin CH2-domain and the immunoglobulin CH3-domain are of the human IgG4 subclass.

10. The polypeptide according to claim 1, wherein the first polypeptide and the second polypeptide further comprise the mutations S228P and L235E.

11. The polypeptide according to claim 1, wherein the first polypeptide and the second polypeptide further comprise the mutation P329G.

12. The polypeptide according to claim 1, wherein the polypeptide is a bispecific antibody.

13. A polypeptide according to claim 1 for intravitreal application.

14. A polypeptide according to claim 1 for the treatment of vascular eye diseases.

15. A pharmaceutical formulation comprising a polypeptide according to claim 1 and optionally a pharmaceutically acceptable carrier.

19. A method for treatment of an eye disease with the polypeptide according to claim 1.

20. A method for the transport of a soluble receptor ligand from the eye over the blood-ocular-barrier into the blood circulation in an individual comprising administering to the individual an effective amount of the polypeptide according to claim 1.

21. A method for the removal of one or more soluble receptor ligands from the eye in an individual comprising administering to the individual an effective amount of the polypeptide according to claim 1.

16-18. -18. (canceled)