Stable and soluble antibodies inhibiting TNFα
View Patent ↗The present invention relates to particularly stable and soluble scFv antibodies and Fab fragments specific for TNFα, which comprise specific light chain and heavy chain sequences that are optimized for stability, solubility, in vitro and in vivo binding of TNFα, and low immunogenicity. Said antibodies are designed for the diagnosis and/or treatment of TNFα-related disorders. The nucleic acids, vectors and host cells for expression of the recombinant antibodies of the invention, methods for isolating them and the use of said antibodies in medicine are also disclosed.
1. A stable and soluble antibody which specifically binds TNFα, said antibody comprising a light chain variable domain (VL) comprising the sequence of SEQ ID NO:1 and a heavy chain variable domain (VH) comprising the sequence of SEQ ID NO:2, or an antigen-binding derivative thereof, wherein said derivative has at maximum up to five amino acid changes as compared to SEQ ID NO: 1 and/or at maximum up to nine amino acid changes as compared to SEQ ID NO: 2, wherein said changes occur at amino acid positions in framework regions of said VL comprising the sequence of SEQ ID NO: 1 and said VH comprising the sequence of SEQ ID NO: 2, and wherein said derivative does not comprise the entire sequences of SEQ ID NO: 3 and SEQ ID NO: 4.
2. The antigen-binding derivative of claim 1 , wherein the up to 5 changes of VL are at any of the positions 4, 46, 65, 67, 70, and 83 and the up to 9 changes of VH are at any of the positions 11, 16, 28, 43, 68, 70, 71, 72, 73, 76, 77, 93 and 112.
3. The antigen-binding derivative of claim 1 , wherein the up to 5 changes of VL are at any of the positions 4, 46, 65, 67, 70, and 83 and the up to 9 changes of VH are at any of the positions 11, 16, 28, 43, 48, 68, 70, 71, 72, 73, 76, 77, 79, 93 and 112.
4. The antigen-binding derivative of claim 1 , in which at least one of the changes leads to an amino acid present in SEQ ID NO:3 at a corresponding position in SEQ ID NO: 1 for VL and/or leads to an amino acid present in SEQ ID NO:4 at a corresponding position in SEQ ID NO: 2 for VH, wherein said derivative does not comprise the entire sequences of SEQ ID NO: 3 and SEQ ID NO: 4.
5. The antibody or antigen-binding derivative of claim 1 , wherein the VL domain comprises the sequence of SEQ ID NO: 1.
6. The antibody or antigen-binding derivative of claim 5 comprising the VH domain of the sequence of SEQ ID NO:2.
7. The antigen-binding derivative of claim 5 comprising a VH domain derived from the sequence of SEQ ID NO:2, wherein F68 is changed to A, L, I, or V.
8. The antigen-binding derivative of claim 1 comprising the VL domain of the sequence of SEQ ID NO:11, and the VH domain of the sequence of SEQ ID NO:4.
9. The antigen-binding derivative according to claim 1 , which is an scFv antibody wherein the VL and VH domains are connected by a linker.
10. The scFv antibody according to claim 9 comprising a VL-linker-VH sequence arrangement.
11. The scFv antibody according to claim 9 , wherein the linker has the sequence of SEQ ID NO:10 or is derived from said sequence.
12. The scFv antibody of claim 11 , wherein at least one G of said linker is changed to a more polar or charged amino acid.
13. The scFv antibody of claim 12 , wherein the linker has the sequence of SEQ ID NO:39.
14. The antigen-binding derivative according to claim 1 , which is a Fab fragment wherein the VL domain is fused to the constant region of a human Ig kappa chain, the VHdomain is fused to the CH1 domain of a human IgG, and the two fusion polypeptides are connected by an inter-chain disulfide bridge.
15. The scFv antibody or Fab fragment according to claim 9 or 14 , which is labeled or chemically modified.
16. A pharmaceutical composition comprising the antibody or antigen-binding derivative of claim 1 as a pharmaceutical.
17. The pharmaceutical composition of claim 16 for the production of a medicament for the treatment of or as an in vitro diagnostic for detection of TNFα-associated diseases, in particular osteoarthritis, uveitis, inflammatory bowel disease.
18. A diagnostic or therapeutic composition comprising an antibody or antigen-binding derivative of claim 1 in combination with a pharmaceutically acceptable carrier, diluent or excipient.
19. The pharmaceutical composition of claim 16 together with at least a second compound.
20. The pharmaceutical composition of claim 19 wherein the second compound is not an antibody specific for TNFα.
21. The pharmaceutical composition of claim 19 for the use as a medicament.
22. A stable aqueous pharmaceutical formulation comprising a therapeutically effective amount of an antibody or antigen-binding derivative of claim 1 not subjected to prior lyophilization, an acetate buffer from about pH 4.8 to about 5.5, a surfactant and a polyol, wherein the formulation lacks a tonicifying amount of sodium chloride.
23. The formulation of claim 22 which is isotonic.
24. The formulation of claim 22 which is stable at a temperature of about 2-8° C. for at least one year.
25. The formulation of claim 22 which is stable following freezing and thawing of the formulation.
26. The formulation of claim 22 which is stable at about 30° C. for at least one month.
27. The formulation of claim 22 wherein the polyol is a non-reducing sugar.
28. The formulation of claim 27 wherein the non-reducing sugar is trehalose.
29. The formulation of claim 27 wherein the non-reducing sugar is sucrose.
30. The formulation of claim 22 wherein the antibody or antigen-binding derivative is an antibody fragment.
31. The formulation of claim 30 wherein the antibody fragment is a scFv.
32. The formulation of claim 22 which is stable at a temperature of about 2-8° C. for at least two years.
33. The formulation of claim 22 wherein the antibody concentration in the formulation is from about 0.1 to about 50 mg/ml.
34. The formulation of claim 22 wherein the surfactant is a polysorbate.
35. The formulation of claim 22 wherein the acetate is present in an amount of about 5-30 mM.
36. The formulation of claim 35 wherein the acetate is present in an amount of 10-30 mM.
37. The formulation of claim 31 further comprising a preservative.
38. The formulation of claim 37 wherein the preservative is benzyl alcohol.
39. The formulation of claim 31 wherein the antibody or antigen-binding derivative is present in an amount of about 30-50 mg/ml.
40. The formulation of claim 39 wherein the buffer is 10-30 mM sodium acetate at pH 5, the polyol is trehalose in an amount of about 2-10% w/v, the surfactant is polysorbate in an amount of about 0.01-0.1% v/v, wherein the formulation further comprises benzyl alcohol as a preservative and wherein the formulation is stable at a temperature of about 2-8° C. for at least two years.
41. An article of manufacture comprising a container holding a stable aqueous pharmaceutical formulation comprising a therapeutically effective amount of an antibody or antigen-binding derivative of claim 1 , not subjected to prior lyophilization, an acetate buffer from about pH 4.8 to about 5.5, a surfactant and a polyol, wherein the formulation lacks a tonicifying amount of sodium chloride.