IP Library Granted Patent US 9,868,948
Granted Patent B2
US 9,868,948 · App. 13/889,484 · Granted Jan 16, 2018

Antigen-binding molecule capable of binding to two or more antigen molecules repeatedly

Inventors: Tomoyuki Igawa (Shizuoka, JP); Shinya Ishii (Shizuoka, JP); Atsuhiko Maeda (Shizuoka, JP); Takashi Nakai (Shizuoka, JP)
Assignee: Chugai Seiyaku Kabushiki Kaisha
C12N15/1037A61K39/12A61K39/145C07K16/244C07K16/248C07K16/2866G01N33/6854A61K2039/505A61K2039/544A61K2039/545A61K2039/552C07K2317/24C07K2317/56C07K2317/565C07K2317/622C07K2317/76C07K2317/77C07K2317/92C12N2760/16111C12N2760/16134C12N2770/20071G01N2500/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,868,948
App. No.
13/889,484
Granted
Jan 16, 2018
Kind
B2
Abstract

The present inventors discovered that antibodies having weaker antigen-binding activity at the early endosomal pH in comparison with that at the pH of plasma are capable of binding to multiple antigen molecules with a single antibody molecule, have long half-lives in plasma, and have improved durations of time in which they can bind to antigen.

Claims (70)

1. A method for producing a pharmaceutical composition comprising an antibody, the method comprising:

(a) determining the binding activity of an antibody to an antigen at a first pH that is in the range of pH 6.7 to pH 10.0, wherein the antibody is a molecule comprising an antigen-binding domain and an Fc domain that has FcRn-binding activity, and wherein the antibody binds the antigen through the antigen-binding domain;

(b) determining the binding activity of the antibody to the antigen at a second pH that is in the range of pH 4.0 to pH 6.5;

(c) determining that the binding activity of the antibody to the antigen at the first pH is greater than that at the second pH;

(d) obtaining nucleic acid comprising coding sequence encoding the antibody of (c);

(e) producing the antibody using the nucleic acid obtained in (d), wherein the produced antibody binds to the antigen in plasma in vivo and dissociates from the bound antigen under conditions present in an endosome in vivo; and

(f) formulating the antibody produced in (e) in a pharmaceutical composition.

2. The method of claim 1 , comprising, prior to (a),

(i) providing starting nucleic acid encoding a starting antibody;

(ii) mutating the starting nucleic acid to substitute at least one non-histidine codon of the coding sequence with a histidine codon, or to insert at least one histidine codon into the coding sequence, thereby producing mutated nucleic acid that encodes a mutant antibody; and

(iii) producing the mutant antibody using the mutated nucleic acid,

wherein the mutant antibody is the antibody of (a).

3. The method of claim 1 , comprising assaying the mean retention time in plasma in vivo of the antibody produced in step (e).

4. The method of claim 1 , comprising assaying the rate of elimination of the antigen from plasma in vivo following administration of the antibody produced in step (e).

5. The method of claim 1 , wherein the antibody is a chimeric antibody.

6. The method of claim 1 , wherein the antibody is a humanized antibody.

7. The method of claim 1 , wherein the antibody is a bispecific antibody.

8. The method of claim 1 , wherein the antibody is a human antibody.

9. A method for producing a pharmaceutical composition comprising an antibody, the method comprising:

(a) contacting an antibody with an antigen at a first pH that is in the range of pH 6.7 to pH 10.0, to form an antigen-antibody complex, wherein the antibody is a molecule comprising an antigen-binding domain and an Fc domain that has FcRn-binding activity, and wherein the antibody binds to the antigen through the antigen-binding domain;

(b) exposing the antigen-antibody complex to a second pH that is in the range of pH 4.0 to pH 6.5;

(c) collecting the antibody that dissociates from the complex at the second pH;

(d) obtaining nucleic acid comprising a coding sequence encoding the antibody collected in (c);

(e) producing the antibody using the nucleic acid obtained in (d), wherein the produced antibody binds to the antigen in plasma in vivo and dissociates from the bound antigen under conditions present in an endosome in vivo; and

(f) formulating the antibody produced in (e) in a pharmaceutical composition.

10. The method of claim 9 , comprising, prior to (a),

(i) providing starting nucleic acid encoding a starting antibody;

(ii) mutating the starting nucleic acid to substitute at least one non-histidine codon of the coding sequence with a histidine codon, or to insert at least one histidine codon into the coding sequence, thereby producing mutated nucleic acid that encodes a mutant antibody; and

(iii) producing the mutant antibody using the mutated nucleic acid,

wherein the mutant antibody is the antibody of (a).

11. The method of claim 9 , wherein the antibody in step (a) is comprised in an antibody library.

12. The method of claim 9 , further comprising assaying the mean retention time in plasma in vivo of the antibody produced in step (e).

13. The method of claim 9 , further comprising assaying the rate of elimination of the antigen from plasma in vivo following administration of the antibody produced in step (e).

14. The method of claim 9 , wherein the antibody is a chimeric antibody.

15. The method of claim 9 , wherein the antibody is a humanized antibody.

16. The method of claim 9 , wherein the antibody is a bispecific antibody.

17. The method of claim 9 , wherein the antibody is a human antibody.

18. A method for producing a pharmaceutical composition comprising an antibody, the method comprising:

(a) binding an antibody, at a first pH, to an antigen that is immobilized on a column, wherein the antibody is a molecule comprising an antigen-binding domain and an Fc domain that has FcRn-binding activity, and wherein the antibody binds to the antigen through the antigen-binding domain;

(b) eluting the antibody from the column at a second pH different from the first pH;

(c) collecting the eluted antibody of (b);

(d) obtaining nucleic acid comprising a coding sequence encoding the antibody collected in (c);

(e) producing the antibody using the nucleic acid obtained in (d), wherein the produced antibody binds to the antigen in plasma in vivo and dissociates from the bound antigen under conditions present in an endosome in vivo; and

(f) formulating the antibody produced in (e) in a pharmaceutical composition.

19. The method of claim 18 , comprising, prior to (a),

(i) providing starting nucleic acid encoding a starting antibody;

(ii) mutating the starting nucleic acid to substitute at least one non-histidine codon of the coding sequence with a histidine codon, or to insert at least one histidine codon into the coding sequence, thereby producing mutated nucleic acid that encodes a mutant antibody; and

(iii) producing the mutant antibody using the mutated nucleic acid,

wherein the mutant antibody is the antibody of (a).

20. The method of claim 18 , wherein the antibody in step (a) is comprised in an antibody library.

21. The method of claim 18 , further comprising assaying the mean retention time in plasma in vivo of the antibody produced in step (e).

22. The method of claim 18 , further comprising assaying the rate of elimination of the antigen from plasma in vivo following administration of the antibody produced in step (e).

23. The method of claim 18 , wherein the antibody is a chimeric antibody.

24. The method of claim 18 , wherein the antibody is a humanized antibody.

25. The method of claim 18 , wherein the antibody is a bispecific antibody.

26. The method of claim 18 , wherein the antibody is a human antibody.

27. A method for producing a pharmaceutical composition comprising an antibody, the method comprising:

(a) contacting an antibody library, at a first pH, with an antigen that is immobilized on a column, wherein antibodies of the library each comprise an antigen-binding domain and an Fc domain that has FcRn-binding activity, and wherein the antibodies of the library bind to the antigen through the antigen-binding domain, and wherein at least one antibody of the library binds to the column at the first pH;

(b) eluting from the column at a second pH an antibody that was bound to the column at the first pH, wherein the second pH is different from the first pH;

(c) collecting the eluted antibody;

(d) obtaining nucleic acid comprising coding sequence encoding the antibody collected in (c);

(e) using the nucleic acid to produce the encoded antibody, wherein the produced antibody is a molecule that binds to the antigen in plasma in vivo and dissociates from the bound antigen under conditions present in an endosome in vivo;

(f) formulating the antibody produced in (e) in a pharmaceutical composition.

28. The method of claim 27 , further comprising assaying the mean retention time in plasma in vivo of the antibody produced in step (e).

29. The method of claim 27 , further comprising assaying the rate of elimination of the antigen from plasma in vivo following administration of the antibody produced in step (e).

30. The method of claim 27 , wherein the antibody is a chimeric antibody.

31. The method of claim 27 , wherein the antibody is a humanized antibody.

32. The method of claim 27 , wherein the antibody is a bispecific antibody.

33. The method of claim 27 , wherein the antibody is a human antibody.

34. The method of claim 27 , wherein the antibody library comprises a plurality of antibodies that bind to the antigen and that differ from each other by the presence of a histidine residue or residues at one or more positions in the various antibodies.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2013
From: IGAWA, TOMOYUKI; ISHII, SHINYA; MAEDA, ATSUHIKO; NAKAI, TAKASHI
To: CHUGAI SEIYAKU KABUSHIKI KAISHA
Reel/Frame 030380/0359 →
Priority Claims (3)
JP 2008-104147 · Apr 11, 2008 · national
JP 2008-247713 · Sep 26, 2008 · national
JP 2009-068744 · Mar 19, 2009 · national
Continuity (3)
Division 13595139 · Aug 27, 2012
Continuation 12936587
Related Publication 20130303396A1 · Nov 14, 2013