Antibodies specific to FcRn
The disclosure relates to antibodies specific to FcRn, formulations comprising the same, use of each in therapy, processes for expressing and optionally formulating said antibody, DNA encoding the antibodies and hosts comprising said DNA.
1. An anti-FcRn antibody or binding fragment thereof comprising (i) a heavy chain or heavy chain fragment having a variable region, and (ii) a complementary light chain or light chain fragment having a variable region, wherein said heavy chain variable region comprises three CDRs, wherein CDR H1 has the sequence given in SEQ ID NO: 1, CDR H2 has the sequence given in SEQ ID NO: 2, and CDR H3 has the sequence given in SEQ ID NO: 3, and wherein said light chain variable region comprises three CDRs, wherein CDR L1 has the sequence given in SEQ ID NO: 4, CDR L2 has the sequence given in SEQ ID NO: 5 or SEQ ID NO: 7 and CDR L3 has the sequence given in SEQ ID NO: 6.
2. The anti-FcRn antibody or binding fragment thereof according to claim 1 having a heavy chain comprising the sequence given in SEQ ID NO:12 and a light chain comprising the sequence given in SEQ ID NO: 8.
3. The anti-FcRn antibody or binding fragment thereof according to claim 1 , wherein the antibody is humanized.
4. The anti-FcRn antibody or binding fragment thereof according to claim 1 having a heavy chain comprising the sequence given in SEQ ID NO: 25 and a light chain comprising the sequence given in SEQ ID NO: 16.
5. The anti-FcRn antibody or binding fragment thereof according to claim 1 having a heavy chain comprising the sequence given in SEQ ID NO: 59 and a light chain comprising the sequence given in SEQ ID NO: 51.
6. An anti-FcRn antibody or binding fragment thereof according to claim 1 , wherein the variable domain of the heavy chain comprises a sequence having at least 90% identity or similarity to the sequence given in SEQ ID NO: 25 and wherein the variable domain of the light chain comprises a sequence having at least 90% identity or similarity to the sequence given in SEQ ID NO: 16.
7. The anti-FcRn antibody or binding fragment thereof according to claim 1 , wherein the antibody or binding fragment is a scFv, Fv, Fab or Fab′ fragment.
8. An anti-FcRn antibody Fab′ fragment according to claim 7 having a heavy chain comprising the sequence given in SEQ ID NO: 33 and a light chain comprising the sequence given in SEQ ID NO: 20.
9. An anti-FcRn antibody Fab′ fragment according to claim 7 having a heavy chain comprising the sequence given in SEQ ID NO: 63 and a light chain comprising the sequence given in SEQ ID NO: 55.
10. The anti-FcRn antibody or binding fragment thereof according to claim 1 , wherein the antibody or binding fragment is conjugated to a polymer and said polymer is starch, albumin, or polyethylene glycol.
11. The anti-FcRn antibody or binding fragment thereof according to claim 10 , wherein the polymer is PEG, having a molecular weight in the range of from about 5 to about 50 kDa.
12. The anti-FcRn antibody according to claim 1 , wherein the antibody is a full length antibody.
13. The anti-FcRn antibody according to claim 12 , wherein the full length antibody is selected from the group consisting of an IgG1, IgG4 and IgG4P.
14. The anti-FcRn antibody according to claim 4 having a heavy chain comprising the sequence given in SEQ ID NO: 37, SEQ ID NO:39 or SEQ ID NO:73 and a light chain comprising the sequence given in SEQ ID NO: 20.
15. The anti-FcRn antibody or binding fragment thereof according to claim 1 wherein the antibody or binding fragment thereof is a Fab-dsFv having a heavy chain comprising the sequence given in SEQ ID NO: 42 and a light chain comprising the sequence given in SEQ ID NO: 40.
16. The anti-FcRn antibody or binding fragment thereof according to claim 1 , which blocks binding of human IgG to human FcRn.
17. The anti-FcRn antibody or binding fragment thereof according to claim 1 which does not bind human β2 microglobulin (SEQ ID NO:72).
18. A pharmaceutical composition comprising an anti-FcRn antibody or binding fragment thereof as defined in claim 1 in combination with one or more of a pharmaceutically acceptable excipient, diluent or carrier.
19. The pharmaceutical composition according to claim 18 comprising other active ingredients.
20. A method of treating a patient with an autoimmune disease comprising administering a therapeutically effective amount of an antibody or binding fragment thereof as defined in claim 1 , wherein the autoimmune disease, is selected from the group consisting of myasthenia gravis, Pemphigus vulgaris, Neuromyelitis optica, Guillain-Barré syndrome, lupus, idiopathic thrombocytopenic purpura and thrombotic thrombocytopenic purpura, or combinations thereof.
21. A method of treating a patient with an autoimmune disease comprising administering a therapeutically effective amount of a composition as defined in claim 18 , wherein the autoimmune disease is selected from the group consisting of myasthenia gravis, Pemphigus vulgaris, Neuromyelitis optica, Guillain-Barré syndrome, lupus, idiopathic thrombocytopenic purpura and thrombotic thrombocytopenic purpura, or combinations thereof.
22. An anti-FcRn antibody Fab fragment according to claim 7 having a heavy chain comprising the sequence given in SEQ ID NO: 29 and a light chain comprising the sequence given in SEQ ID NO: 20.