Cytotoxicity-inducing therapeutic agent

Patent metadata

Field	Value
Publication number	US-11066483-B2
Application number	US-201113990088-A
Country	US
Kind code	B2
Filing date	Nov 30, 2011
Priority date	Nov 30, 2010
Publication date	Jul 20, 2021
Grant date	Jul 20, 2021

Abstract

By replacing the antigen-binding domain, the present inventors discovered novel polypeptide complexes that retain BiTE's strong anti-tumor activity and excellent safety properties, as well as have long half-life in blood and can damage various different target cells.

First claim

The invention claimed is:

1. A bispecific antibody that comprises:
a first light chain comprising a first VL domain and a first CL domain;
a second light chain comprising a second VL domain and a second CL domain;
a first heavy chain comprising a first heavy chain variable region and a first heavy chain constant region, wherein the first heavy chain constant region is a non-wild-type heavy chain constant region comprising the sequence of one of SEQ ID NOs: 23, 24, 25 and 26, with one or more amino acid substitutions and optionally a deletion of the amino acids at EU numbering positions 446 and 447; and
a second heavy chain comprising a second heavy chain variable region and a second heavy chain constant region, wherein the second heavy chain constant region is a non-wild-type heavy chain constant region comprising the sequence of one of SEQ ID NOs: 23, 24, 25 and 26, with one or more amino acid substitutions and optionally a deletion of the amino acids at EU numbering positions 446 and 447, wherein the amino acid sequence of the second heavy chain constant region is the same as or different from the amino acid sequence of the first heavy chain constant region, and is of the same isotype as the first heavy chain constant region;
wherein the first light chain and the first heavy chain associate to form a first antigen- binding domain that binds to CD3,
wherein the second light chain and the second heavy chain associate to form a second antigen-binding domain that does not bind to CD3, and that does bind to a cancer antigen that is not CD3,
wherein the first heavy chain constant region associates with the second heavy chain constant region,
wherein, when assessed by a surface plasmon resonance technique, the ability of the associated first and second heavy chain constant regions to bind to a given human Fcγ receptor is reduced, compared to the ability of a wild-type human IgG antibody of the same isotype as the bispecific antibody to bind to the human Fcγ receptor, as a result of at least one of the one or more amino acid substitutions within the first and second heavy chain constant regions,
wherein the at least one substitution in the first and second heavy chain constant regions represents a change in amino acid sequence compared to the amino acid sequence of the heavy chain constant regions of the wild-type human IgG antibody, and
wherein at least one of the amino acid substitutions that result in the reduced ability to bind to the human Fcγ receptor is at a position selected from the following EU numbering positions in each of the first and second heavy chain constant regions: 220, 226, 229, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 264, 265, 266, 267, 269, 270, 295, 296, 297, 298, 299, 300, 325, 327, 328, 329, 330, 331, and 332.

2. The bispecific antibody of claim 1 , wherein
the amino acid sequence from position 118 to position 260 (EU numbering) of the first heavy chain constant region and of the second heavy chain constant region is the sequence from the corresponding portion of SEQ ID NO: 24; or
the amino acid sequence from position 261 to position 447 (EU numbering) of the first heavy chain constant and of the second heavy chain constant region is the sequence from the corresponding portion of SEQ ID NO: 26.

3. The bispecific antibody of claim 1 , wherein the first heavy chain constant region and the second heavy chain constant region each comprises the sequence of SEQ ID NO: 23 with one or more substitutions and optionally a deletion of the two residues at the carboxyl terminus of SEQ ID NO: 23.

4. The bispecific antibody of claim 3 , wherein the one or more substitutions include a substitution in both the first and the second heavy chain constant regions at a position selected from positions 233, 234, 235, 236, 327, 330, and 331 (EU numbering), the substitution at the selected position being by an amino acid from a corresponding position in IgG2 or IgG4.

5. The bispecific antibody of claim 3 , wherein the one or more substitutions include a substitution in both the first and the second heavy chain constant regions at position 234, 235, or 297 (EU numbering).

6. The bispecific antibody of claim 5 , wherein the one or more substitutions include a substitution by alanine.

7. The bispecific antibody of claim 1 , wherein the amino acid sequence of the second heavy chain constant region is different from the amino acid sequence of the first heavy chain constant region.

8. The bispecific antibody of claim 7 , wherein
in one of the two heavy chain constant regions of the bispecific antibody, the amino acids at positions 349 and 366 (EU numbering) are cysteine and tryptophan, respectively; and
in the other heavy chain constant region of the bispecific antibody, the amino acids at positions 356, 366, 368, and 407 (EU numbering) are cysteine, serine, alanine, and valine, respectively.

9. The bispecific antibody of claim 7 , wherein:
in one of the two heavy chain constant regions of the bispecific antibody, the amino acid at position 356 is lysine,
in the other heavy chain constant region of the bispecific antibody, the amino acid at position 439 is glutamic acid; and
in one but not both of the two heavy chain constant regions of the bispecific antibody, the amino acid at position 435 is arginine (all positions being by EU numbering).

10. The bispecific antibody of claim 8 , wherein the amino acids at EU numbering positions 446 and 447 are deleted in both heavy chain constant regions of the bispecific antibody.

11. The bispecific antibody of claim 1 , wherein the human Fcγ receptor is selected from Fcγl, FcγIIA, FcγIIB, FcγIIIA, and FcγIIIB.

12. The bispecific antibody of claim 1 , wherein the amino acid sequence of the second heavy chain constant region is the same as the amino acid sequence of the first heavy chain constant region.

13. The bispecific antibody of claim 1 , wherein the amino acid sequence of the second heavy chain constant region is different from the amino acid sequence of the first heavy chain constant region, and wherein the percentage of heterodimers formed in a mixture of the first and second heavy chains is higher than the percentage of heterodimers that would be formed if the two heavy chain constant regions were identical and matched one of SEQ ID NO: 23-26.

14. The bispecific antibody of claim 13 , wherein the difference between the sequences of the first and second heavy chain constant regions comprises a difference at one or more CH3 domain positions.

15. The bispecific antibody of claim 14 , wherein the difference between the sequences of the first and second heavy chain constant regions further comprises a difference at one or more CH1 domain positions, wherein the one or more CH1 domain positions interface with a CL domain.

16. The bispeciflc antibody of claim 1 , wherein the amino acid sequence of the second heavy chain constant region is different from the amino acid sequence of the frst heavy chain constant region, and this difference in sequences comprises a difference at one or more CH1 domain positions of the two heavy chain constant regions, wherein the one or more CH1 domain positions interface with a CL domain.

17. The bispecific antibody of claim 1 , wherein the human Fcγ receptor is selected from Fcγl, FcγIIIA, and FcγIIIB.

18. The bispecific antibody of claim 1 , wherein, when assessed by a surface plasmon resonance technique, the bispecific antibody's ability to bind to each of human Fcγ receptors Fcγl, FcγIIIA, and FcγIIIB is reduced compared to the ability of a wild-type human IgG antibody of the

Assignees

• Nezu Junichi
• Ishiguro Takahiro
• Narita Atsushi
• Sakamoto Akihisa
• Kawai Yumiko
• Igawa Tomoyuki
• Kuramochi Taichi
• Chugai Pharmaceutical Co Ltd

Inventors

• Nezu Junichi
• Ishiguro Takahiro
• Narita Atsushi
• Sakamoto Akihisa
• Kawai Yumiko
• Igawa Tomoyuki
• Kuramochi Taichi

Classifications

• C07K16/00

  Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies · CPC title

• C07K16/468

  Immunoglobulins having two or more different antigen binding sites, e.g. multifunctional antibodies · CPC title

• A61K38/00

  Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title

• C07K16/18

  against material from animals or humans · CPC title

• C07K16/28

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