IP Library Granted Patent US 9,090,685
Granted Patent B2
US 9,090,685 · App. 14/059,241 · Granted Jul 28, 2015

Antibodies to TGF-beta

Inventors: Steven R. Ledbetter (Westborough, MA); Celia Patricia Hart (Noyarey, FR); Robert G. Holgate (Royston, GB); Lutz U. Jermutus (Buckhurst Hill, GB); Catriona L. Buchanan (Sawston, GB); Alexander R. Duncan (Girton, GB); Donna K. Finch (Horseheath, GB)
Assignees: Genzyme Corporation; Optein, Inc.
C07K16/22A61K2039/505C07K2316/96C07K2317/21C07K2317/565C07K2317/622C07K2317/73C07K2317/74
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Quick Facts
Patent No.
US 9,090,685
App. No.
14/059,241
Granted
Jul 28, 2015
Kind
B2
Abstract

The present invention relates to antibody molecules, in particular antibody molecules that bind Transforming Growth Factor beta (TGFβ), and uses thereof. More particularly, the invention relates to antibody molecules that bind and preferably neutralize TGFβ1, TGFβ2 and TGFβ3, so-called “pan-specific” antibody molecules, and uses of such antibody molecules. Preferred embodiments within the present invention are antibody molecules, whether whole antibody (e.g. IgG, such as IgG1 or IgG4) or antibody fragments (e.g. scFv, Fab, dAb).

Claims (27)

1. An isolated nucleic acid encoding the heavy chain, the light chain, or both, of a specific binding member that binds to human TGFβ1, TGFβ2 and TGFβ3, said specific binding member comprising an antigen-binding portion of an antibody

wherein the heavy chain of the antibody comprises an HCDR1 comprising the amino acid sequence of SEQ ID NO: 3, an HCDR2 comprising the amino acid sequence of SEQ ID NO: 4, and an HCDR3 comprising the amino acid sequence of SEQ ID NO: 5; and

wherein the light chain of the antibody comprises an LCDR1 comprising the amino acid sequence of SEQ ID NO: 8, an LCDR2 comprising the amino acid sequence of SEQ ID NO: 9, and an LCDR3 comprising the amino acid sequence of SEQ ID NO: 10.

2. The isolated nucleic acid according to claim 1 , wherein the specific binding member is an antibody comprising:

a) the PET1073G12 V H domain (SEQ ID NO: 2);

b) the PET1073G12 V L domain (SEQ ID NO: 7); or

c) both a) and b).

3. The isolated nucleic acid according to claim 2 , wherein the antibody further comprises a human IgG4 constant region.

4. The isolated nucleic acid according to claim 2 , wherein the antibody further comprises a human IgG1 constant region.

5. The isolated nucleic acid according to claim 1 , wherein the specific binding member is a single chain Fv molecule comprising:

a) the PET1073G12 V H domain (SEQ ID NO: 2);

b) the PET1073G12 V L domain (SEQ ID NO: 7); or

c) both a) and b).

6. The isolated nucleic acid according to claim 1 , wherein the specific binding member neutralizes human TGFβ1, TGFβ2 and TGFβ3.

7. The isolated nucleic acid according to claim 1 , wherein the heavy chain of the antibody comprises an FR4 amino acid sequence comprising the amino acid sequence of SEQ ID NO: 31.

8. The isolated nucleic acid according to claim 1 , wherein the antibody comprises the PET1073G12 V H domain (SEQ ID NO: 2) with up to 5 framework mutations.

9. The isolated nucleic acid according to claim 1 , wherein the antibody comprises the PET1073G12 V L domain (SEQ ID NO: 7) with up to 5 framework mutations.

10. The isolated nucleic acid according to claim 1 , wherein the specific binding member is an antibody, wherein the heavy chain of the antibody comprises the PET1073G12 V H domain (SEQ ID NO: 2) and a human IgG4 constant region, and wherein the light chain of the antibody comprises the PET1073G12 V L domain (SEQ ID NO: 7) and a human κ light chain constant region.

11. A host cell transformed with the nucleic acid according to claim 1 or 10 .

12. A method of producing a specific binding member, comprising:

culturing a host cell according to claim 11 under conditions for production of said specific binding member, and

isolating and/or purifying said specific binding member,

wherein the host cell comprises a nucleotide sequence encoding the heavy chain, and a nucleotide sequence encoding the light chain, of the antigen-binding portion of the antibody.

13. The method according to claim 12 , further comprising formulating the specific binding member into a composition including at least one additional active component.

14. The method according to claim 12 , wherein the specific binding member is an scFv antibody molecule.

15. The method according to claim 12 , wherein the specific binding member is an Fab antibody molecule.

16. The method according to claim 12 , wherein the specific binding member is a whole antibody.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2015
From: HART, CELIA PATRICIA; HOLGATE, ROBERT GEORGE EDWARD; JERMUTUS, LUTZ ULRICH JOCHEN WILHELM; BUCHANAN, CATRIONA LOUISE; DUNCAN, ALEXANDER ROBERT; FINCH, DONNA KIRSTY
To: CAMBRIDGE ANTIBODY TECHNOLOGY LIMITED
Reel/Frame 034905/0212 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2015
From: CAMBRIDGE ANTIBODY TECHNOLOGY LIMITED
To: OPTEIN, INC.
Reel/Frame 034905/0263 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2015
From: LEDBETTER, STEVEN R.
To: GENZYME CORPORATION
Reel/Frame 034905/0275 →
Continuity (5)
Division 13615388 · Sep 13, 2012
Division 12724347 · Mar 15, 2010
Continuation 11350906 · Feb 8, 2006
Provisional Application 60651343 · Feb 8, 2005
Related Publication 20140127230A1 · May 8, 2014