Antagonist antibodies that bind to human TGFB1, TGFB2 and to TGFB3 and their use for the treatment of lung fibrosis
The present disclosure relates to TGF-beta antibodies and binding fragments thereof, DNA encoding the same, host cells comprising said DNA and methods of expressing the antibody or binding fragment in a host cell. The disclosure also extends to pharmaceutical compositions comprising the antibody or a binding fragment thereof and use of the antibody, binding fragment and compositions comprising the same in treatment of various diseases including fibrosis.
1. An antagonistic antibody, or a binding fragment thereof, which binds human TGF-beta 1, human TGF-beta 2 and human TGF-beta 3 comprising a heavy chain and a light chain wherein the variable domain of the heavy chain comprises a CDR having the sequence given in SEQ ID NO:4 for CDR-H1, a CDR having the sequence given in SEQ ID NO:5 for CDR-H2 and a CDR having the sequence given in SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8 or SEQ ID NO:9 for CDR-H3, and wherein the variable domain of the light chain comprises a CDR having the sequence given in SEQ ID NO:1 for CDR-L1, a CDR having the sequence given in SEQ ID NO:2 for CDR-L2 and a CDR having the sequence given in SEQ ID NO:3 for CDR-L3.
2. The antibody, or a binding fragment thereof, according to claim 1 , wherein the antibody comprises a heavy chain comprising the sequence given in SEQ ID NO:52, SEQ ID NO:66, SEQ ID NO:80 or SEQ ID NO:94.
3. The antibody, or a binding fragment thereof, according to claim 1 , wherein the antibody comprises a light chain comprising the sequence given in SEQ ID NO:38.
4. The antibody, or a binding fragment thereof, according to claim 1 , selected from the group consisting of a complete antibody molecule having full length heavy and light chains, a Fab, modified Fab′, Fab′, F(ab′)2, Fv, and scFv.
5. The antibody, or a binding fragment thereof, according to claim 1 , having a binding affinity for human TGF-beta 1 of 200 pM or better, a binding affinity for human TGF-beta 2 of 300 pM or better and a binding affinity for human TGF-beta 3 of 2500 pM or better.
6. The antibody, or a binding fragment thereof, according to claim 1 , that is a monoclonal humanized antibody.
7. A pharmaceutical composition comprising an antibody, or a binding fragment thereof, according to claim 1 in combination with one or more of a pharmaceutically acceptable excipient, diluent or carrier.
8. A method for the treatment of a human subject suffering from kidney fibrosis or pulmonary fibrosis, the method comprising administering to the subject an effective amount of an antibody, or a binding fragment thereof, according to claim 1 , wherein extracellular matrix (ECM) deposition is inhibited.
9. The method according to claim 8 , wherein the binding fragment thereof is a Fab or Fab′ fragment which binds human TGF-beta 1, human TGF-beta 2 and human TGF-beta 3 and is administered by inhalation.
10. An antagonistic antibody, or a binding fragment thereof, which binds human TGF-beta 1, human TGF-beta 2 and human TGF-beta 3, having a heavy chain comprising the sequence given in SEQ ID NO:52, SEQ ID NO:59, SEQ ID NO:66, SEQ ID NO:73, SEQ ID NO:80, SEQ ID NO:87, SEQ ID NO:94, or SEQ ID NO:101 and a light chain comprising the sequence given in SEQ ID NO:38 or SEQ ID NO:45.
11. A process for the production of an antagonistic antibody, or a binding fragment thereof, which binds human TGF-beta 1, human TGF-beta 2 and human TGF-beta 3 comprising a heavy chain and a light chain, wherein the variable domain of the heavy chain comprises a CDR having the sequence given in SEQ ID NO:4 for CDR-H1, a CDR having the sequence given in SEQ ID NO:5 for CDR-H2 and a CDR having the sequence given in SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8 or SEQ ID NO:9 for CDR-H3, and wherein the variable domain of the light chain comprises a CDR having the sequence given in SEQ ID NO:1 for CDR-L1, a CDR having the sequence given in SEQ ID NO:2 for CDR-L2 and a CDR having the sequence given in SEQ ID NO:3 for CDR-L3, comprising culturing a host cell expressing said antibody and isolating said antibody.