CL and/or CH1 mutated antibodies for drug conjugation

Patent metadata

Field	Value
Publication number	US-11833222-B2
Application number	US-202017019537-A
Country	US
Kind code	B2
Filing date	Sep 14, 2020
Priority date	Feb 16, 2015
Publication date	Dec 5, 2023
Grant date	Dec 5, 2023

Abstract

Antibodies having modified constant regions so as to permit conjugation of the antibody to a payload such as a therapeutic agent are described. Preferred antibodies include a mutation at light chain position 180 (positional numbering), most preferably the mutation is to a residue selected from C, K, Q, or a non-natural amino acid. Additional mutations may also be combined with a mutation at position 180; including one or more of light chain (LC) S208, LC S171, LC S182, LC A184, LC V191, LC S202, LC S203, LC T206, heavy chain (HC) S160, HC T190, HC S443, HC S447, HC S139, HC S168, HC V170, HC V176, HC T200, HC S445 according to a positional numbering convention.

First claim

The invention claimed is:

1. An antibody, or a fragment or derivative thereof, having a variable region which binds a target molecule, and a constant region, wherein the constant region comprises one or more mutations introducing a site specific conjugation site selected so as to permit conjugation of the antibody, fragment, or derivative to a payload, wherein the antibody comprises the amino acid sequence of SEQ ID NO: 36; where X is selected from C, K, or Q.

2. The antibody of claim 1 , wherein the antibody is selected from the group comprising IgG1, IgG2, IgG3, and IgG4.

3. The antibody of claim 2 , wherein the constant region comprises one or more of the Ck, CH1 and CH3 domains of the IgG1 constant region.

4. The antibody of claim 1 , wherein the antibody is selected from the group consisting of Fabs, bi specific antibody fragments (tandem scFv-Fc, scFv-Fc knobs-into-holes, scFv-Fc-scFv, F(ab′)2, Fab-scFv, (Fab′scFv)2, scDiabody-Fc, or scDiabody-CH3), IgG-based bispecific antibodies (Hybrid hybridoma, Knobs-into-holes with common light chain, Two-in-one IgG, Dual V domain IgG, IgG-scFv, scFv-IgG, IgG-V, V-IgG), minibody, tribi-minibody, nanobodies, and di-diabody.

5. The antibody of claim 1 , wherein the antibody is selected from Abciximab; Rituximab; Basiliximab; Daclizumab; Palivizumab; Infliximab; Trastuzumab; Alemtuzumab; Adalimumab; Efalizumab; Cetuximab; Ibritumomab; Omalizumab; Bevacizumab; Ranibizumab; Golimumab; Canakinumab; Ustekinumab; Tocilizumab; Ofatumumab; Belimumab; Ipilimumab; Brentuximab; Pertuzumab; Raxibacumab; Vedolizumab; Ramucirumab; Obinutuzumab; Siltuximab; Secukinumab; Dinutuximab.

6. The antibody of claim 1 , which lacks one or more Fc effector functions.

7. An immunoconjugate comprising the antibody of claim 1 , a payload, and a linker joining the payload to the antibody.

8. The immunoconjugate of claim 7 , wherein the linker is selected from 6-maleimidocaproyl (MC), maleimidopropanoyl (MP), valine-citrulline (val-cit), alanine-phenylalanine (ala-phe), p-aminobenzyloxycarbonyl (PAB), N-Succinimidyl 4-(2-pyridylthio) pentanoate (SPP), N-succinimidyl 4-(N-maleimidomethyl) cyclohexane-1 carboxylate (SMCC), N-Succinimidyl, (4-iodo-acetyl) aminobenzoate (SIAB),), SPDB, hydrazone, maleimidocaproyl and 6-maleimidocaproyl-valine-citrulline-p-aminobenyloxycarbonyl (MC-vc-PAB); or is a branched linker which comprises a peptide chain and is derived from o-hydroxy p-amino benzylic alcohol, wherein the peptide chain is connected to the phenyl ring via the p-amino group, the payload is connected to the phenyl ring via the benzylic alcohol moiety, and the antibody is connected to the phenyl ring via the o-hydroxy group.

9. The immunoconjugate of claim 7 , wherein the payload is selected from the group consisting of 90Y, 131I, 67Cu, 177Lu, 213Bi, 211At, dolastatin, vedotin, monomethyl auristatin F(MMAF), monomethyl auristatin E (MMAE); maytansinoids including DM1 and DM4, duocarmycin, duocarmycin analogs, calicheamicin, pyrrolobenzodiazepines (PBD), centanamycin, irinotecan, and doxorubicin, alpha-amanitin, melatonin, membrane disrupting peptide, Pseudomonas exotoxin A, Diphtheria toxin, ricin, polyethylene glycol, hydroxyethyl starch, and a mannosyl residue.

10. A pharmaceutical composition comprising an antibody according to claim 1 , and a pharmaceutically acceptable diluent, carrier or excipient.

11. A method for generating an immunoconjugate, the method comprising conjugating the antibody of claim 1 to a payload.

12. An isolated or recombinant polynucleotide encoding the antibody of claim 1 .

13. A vector comprising the polynucleotide of claim 12 .

14. A host cell comprising the vector of claim 13 .

15. A method of producing an antibody comprising:
(a) providing a culture medium comprising the host cell of claim 14 ; and
(b) placing the culture medium in conditions under which the antibody is expressed, and optionally
(c) isolating the antibody.

16. The antibody of claim 1 , further comprising a mutation at one or more of heavy chain positions 160, 190, 168, 170, 176 or 200.

17. The antibody of claim 1 , wherein the light chain is a kappa light chain.

Assignees

• Lonza Ag

Inventors

• Gomez De La Cuesta Ramon
• Zurdo Jesús
• Arnell Lars Arne Andreas
• Ducry Laurent
• Bonnafoux Laurence

Classifications

• C07K2317/73

  Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation · CPC title

• A61K47/6803

  Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates · CPC title

• A61K47/68031

  the drug being an auristatin · CPC title

• A61K47/6855 Primary

  the tumour determinant being from breast cancer cell · CPC title

• A61P35/00

  Antineoplastic agents · CPC title