IP Library Granted Patent US 8,883,980
Granted Patent B2
US 8,883,980 · App. 11/889,975 · Granted Nov 11, 2014

Antigen binding molecules with increased Fc receptor binding affinity and effector function

Inventors: Pablo Umaña (Zurich, CH); Peter Brünker (Hittnau, CH); Claudia Ferrera Koller (Zug, CH); Tobias Suter (Windisch, CH); Ursula Püntener (Baden, CH); Ekkehard Mössner (Kreuzlingen, CH)
Assignee: Roche Glycart AG
C07K16/2887C07K2317/92C07K2317/24C07K2317/41C07K2317/72C07K2317/56C07K2317/734C07K2317/53C07K2317/567C07K2317/52C07K2317/732A61K2039/505Y10S530/808Y10S530/866Y10S530/867
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Quick Facts
Patent No.
US 8,883,980
App. No.
11/889,975
Granted
Nov 11, 2014
Kind
B2
Abstract

The present invention relates to antigen binding molecules (ABMs). In particular embodiments, the present invention relates to recombinant monoclonal antibodies, including chimeric, primatized or humanized antibodies specific for human CD20. In addition, the present invention relates to nucleic acid molecules encoding such ABMs, and vectors and host cells comprising such nucleic acid molecules. The invention further relates to methods for producing the ABMs of the invention, and to methods of using these ABMs in treatment of disease. In addition, the present invention relates to ABMs with modified glycosylation having improved therapeutic properties, including antibodies with increased Fc receptor binding and increased effector function.

Claims (18)

1. An antibody that binds to human CD20 comprising:

(a) a heavy chain variable region (VH) comprising the amino acid sequence of SEQ ID NO:40; and

(b) a light chain variable region (VL) comprising the amino acid sequence of SEQ ID NO:76.

2. The antibody of claim 1 , wherein the antibody comprises a human Fc region.

3. The antibody of claim 2 , wherein the human Fc region is a human IgG1 Fc region.

4. The antibody of claim 2 , wherein the Fc region comprises an N-linked oligosaccharide that has been modified.

5. The antibody of claim 4 , wherein N-linked oligosaccharides of the Fc region have reduced fucose residues as compared to an antibody with non-modified N-linked oligosaccharides.

6. The antibody of claim 4 , wherein the modified N-linked oligosaccharide comprises a bisected oligosaccharide.

7. The antibody of claim 6 , wherein the bisected oligosaccharide is a bisected complex oligosaccharide.

8. The antibody of claim 4 , wherein the modified N-linked oligosaccharide comprises a bisected, nonfucosylated oligosaccharide.

9. The antibody of claim 8 , wherein the bisected, nonfucosylated oligosaccharide is a hybrid type.

10. The antibody of claim 8 , wherein the bisected, nonfucosylated oligosaccharide is a complex type.

11. The antibody of claim 2 , wherein the Fc region comprises an N-linked oligosaccharide lacking fucose.

12. The antibody of claim 1 , wherein the antibody is an antigen-binding fragment.

13. An antibody produced by a method comprising: culturing a host cell comprising one or more polynucleotides encoding an antibody comprising a variable heavy chain region (VH) comprising the amino acid sequence of SEQ ID NO:40 and a variable light chain region (VL) comprising the amino acid sequence of SEQ ID NO:76, under conditions that permit expression of the antibody, wherein the antibody binds to human CD20.

14. The antibody of claim 13 , wherein the method further comprises recovering the antibody expressed by the host cell.

15. The antibody of claim 13 , wherein the host cell is a mammalian cell or a yeast cell.

16. The antibody of claim 15 , wherein the mammalian cell is a CHO cell.

Assignments (1)
CHANGE OF NAME Recorded Sep 9, 2011
From: GLYCART BIOTECHNOLOGY AG
To: ROCHE GLYCART AG
Reel/Frame 026883/0831 →
Continuity (3)
Division 10981738 · Nov 5, 2004
Provisional Application 60517096 · Nov 5, 2003
Related Publication 20090010921A1 · Jan 8, 2009