IP Library Granted Patent US 9,481,726
Granted Patent B2
US 9,481,726 · App. 14/682,975 · Granted Nov 1, 2016

Antibodies to TGF-β

Inventors: Steven R. Ledbetter (Westborough, MA); Celia Patricia Hart (Noyarey, FR); Robert G. Holgate (Hertfordshire, GB); Lutz U. Jermutus (Buckhurst Hill, GB); Catriona L. Buchanan (Sawston, GB); Alexander R. Duncan (Girton, GB); Donna K. Finch (Horseheath, GB)
Assignee: GENZYME CORPORATION
C07K16/22A61K2039/505C07K2316/96C07K2317/21C07K2317/565C07K2317/567C07K2317/622C07K2317/64C07K2317/73C07K2317/74C07K2317/76
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Quick Facts
Patent No.
US 9,481,726
App. No.
14/682,975
Granted
Nov 1, 2016
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 (20)

1. A method of treating pulmonary fibrosis or lung fibrosis with an isolated specific binding member that binds TGFβ1, TGFβ2, AND TGFβ3, said binding member comprising an antigen-binding domain of an antibody,

wherein the heavy chain of said 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 said 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 method of claim 1 , wherein the antibody comprises the PET1073G12 VH domain (SEQ ID NO: 2) and the PET1073G12 VL domain (SEQ ID NO: 7).

3. The method of claim 2 , wherein the antibody further comprises a human IgG4 constant region.

4. The method of claim 2 , wherein the antibody further comprises a human IgG1 constant region.

5. The method of claim 1 , wherein the isolated specific binding member comprises an isolated single chain Fv molecule comprising the PET1073G12 VH domain (SEQ ID NO: 2) and the PET1073G12 VL domain (SEQ ID NO: 7).

6. The method of claim 1 , wherein the antibody comprises the PET1073G12 VH domain (SEQ ID NO: 2).

7. The method of claim 1 , wherein the antibody comprises the PET1073G12 VL domain (SEQ ID NO: 7).

8. The method of claim 1 , wherein the antibody comprises a heavy chain comprising the PET1073G12 VH domain (SEQ ID NO: 2) and a human IgG4 constant region, and a light chain comprising the PET1073G12 VL domain (SEQ ID NO: 7) and a human κ light chain constant region.

9. The method of claim 1 , wherein the isolated specific binding member neutralizes human TGFβ1, TGFβ2 and TGFβ3.

10. The method of claim 1 , wherein said heavy chain comprises an FR4 amino acid sequence comprising the amino acid sequence in SEQ ID NO: 31.

11. The method of claim 1 , wherein the antibody comprises the PET1073G12 VH domain (SEQ ID NO: 2) with up to 5 framework mutations.

12. The method of claim 1 , wherein the antibody comprises the PET1073G12 VL domain (SEQ ID NO: 7) with up to 5 framework mutations.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2016
From: LEDBETTER, STEVEN R.
To: GENZYME CORPORATION
Reel/Frame 038343/0082 →
Continuity (6)
Division 14059241 · Oct 21, 2013
Division 13615388 · Sep 13, 2012
Division 12724347 · Mar 15, 2010
Continuation 11350906 · Feb 8, 2006
Provisional Application 60651343 · Feb 8, 2005
Related Publication 20150284456A1 · Oct 8, 2015