Immunotoxin for treating cancer

Patent metadata

Field	Value
Publication number	US-11713352-B2
Application number	US-202117225953-A
Country	US
Kind code	B2
Filing date	Apr 8, 2021
Priority date	Apr 30, 2003
Publication date	Aug 1, 2023
Grant date	Aug 1, 2023

Abstract

The present invention relates to methods for preventing or treating head and neck spuamous cell cancer and bladder cancer using an immunotoxin comprising (a) a ligand that binds to a protein on the cancer cell attached to; (b) a toxin that is cytotoxic to the cancer cell. In a specific embodiment, the invention is directed to the prevention or treatment of head and neck squamous cell cancer or bladder cancer using Vb4-845, which is a recombinant immunotoxin comprising a humanized, MOC31-derived, single-chain antibody fragment that is fused to a truncated form of Pseudomonas exotoxin A. Also encompassed by the invention are combination therapy methods, including the use of reduced dosages of chemotherapeutic agents, for the prevention or treatment of cancer. Also encompassed by the invention are formulations and methods for direct administration of the recombinant immunotoxin to the carcinoma, for the prevention or treatment of cancer.

First claim

The invention claimed is:

1. An immunotoxin that binds to EPCAM wherein the immunotoxin comprises a framework region and CDRS and an endotoxin, wherein the immunotoxin comprises amino acid residues 29-659 of SEQ ID NO: 2.

2. An immunotoxin that binds to EPCAM wherein the immunotoxin comprises a framework region and CDRS and an endotoxin, wherein the CDRs are as follows:
Heavy chain CDR1 consisting of amino acids residues 197-201 of SEQ ID NO:2;
Heavy chain CDR2 consisting of amino acids residues 216-232 of SEQ ID NO:2;
Heavy chain CDR3 consisting of amino acids residues 265-271 of SEQ ID NO:2;
Light chain CDR1 consisting of amino acids residues 52-67 of SEQ ID NO:2;
Light chain CDR2 consisting of amino acids residues 83-89 of SEQ ID NO:2; and
Light chain CDR3 consisting of amino acids residues 122-130 of SEQ ID NO:2; and
wherein the endotoxin comprises amino acid residues 303-659 of SEQ ID NO:2.

3. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 97 of SEQ ID NO: 2 is SER.

4. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 99 of SEQ ID NO: 2 is GLY.

5. The immunotoxin of claim 1 wherein the framework region comprises mutations wherein amino acid residue 97 of SEQ ID NO: 2 is SER and wherein amino acid residue 99 of SEQ ID NO: 2 is GLY.

6. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 172 of SEQ ID NO: 2 is GLN.

7. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 175 of SEQ ID NO: 2 is PRO.

8. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 184 of SEQ ID NO: 2 is VAL.

9. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 186 of SEQ ID NO: 2 is ILE.

10. The immunotoxin of claim 1 wherein the framework region comprises mutations wherein amino acid residue 193-196 of SEQ ID NO: 2 are TYR, THR, PHE, and THR.

11. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 204 of SEQ ID NO: 2 is LYS.

12. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residues 214-215 of SEQ ID NO: 2 are MET and GLY.

13. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 236 of SEQ ID NO: 2 is PHE.

14. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 238 of SEQ ID NO: 2 is LEU.

15. The immunotoxin of claim 1 wherein the framework region comprises mutations wherein amino acid residues 242-244 of SEQ ID NO: 2 are ALA, SER, and ALA.

16. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 249 of SEQ ID NO: 2 is ILE.

17. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 263 of SEQ ID NO: 2 is ALA.

18. The immunotoxin of claim 1 wherein the framework region comprises a mutation wherein amino acid residue 278 of SEQ ID NO: 2 is LEU.

19. The immunotoxin of claim 1 wherein the framework region comprises mutations:
wherein amino acid residue 172 of SEQ ID NO: 2 is GLN;
wherein amino acid residue 175 of SEQ ID NO: 2 is PRO;
wherein amino acid residue 184 of SEQ ID NO: 2 is VAL;
wherein amino acid residue 186 of SEQ ID NO: 2 is ILE;
wherein amino acid residue 193-196 of SEQ ID NO: 2 are TYR, THR, PHE, and THR;
wherein amino acid residue 204 of SEQ ID NO: 2 is LYS;
wherein amino acid residues 214-215 of SEQ ID NO: 2 are MET and GLY;
wherein amino acid residue 236 of SEQ ID NO: 2 is PHE;
wherein amino acid residue 238 of SEQ ID NO: 2 is LEU;
wherein amino acid residues 242-244 of SEQ ID NO: 2 are ALA, SER, and ALA;
wherein amino acid residue 249 of SEQ ID NO: 2 is ILE;
wherein amino acid residue 263 of SEQ ID NO: 2 is ALA; and
wherein amino acid residue 278 of SEQ ID NO: 2 is LEU.

20. The immunotoxin of claim 1 comprising residues 55-141; 167-282; and 303-659 of SEQ ID NO:2.

21. A nucleic acid encoding the amino acid sequence of the immunotoxin of claim 1 .

22. A nucleic acid encoding the amino acid sequence of the immunotoxin of claim 2 .

Assignees

• Univ Zuerich
• Univ Of Zuerich

Inventors

• Zangemeister-Wittke Uwe
• Di Paolo Claudio
• Tschudi Dominique Christine
• Glover Nicholas Ronald
• Fitsialos Dimitri Peter

Classifications

• C07K16/28 Primary

  against receptors, cell surface antigens or cell surface determinants · CPC title

• A61K45/06

  Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title

• A61K47/6829

  Bacterial toxins, e.g. diphteria toxins or Pseudomonas exotoxin A · CPC title

• A61K47/6861

  the tumour determinant being from kidney or bladder cancer cell · CPC title

• A61K47/6865

  the tumour determinant being from skin, nerves or brain cancer cell · CPC title