Method for altering plasma retention and immunogenicity of antigen-binding molecule

Patent metadata

Field	Value
Publication number	US-11718678-B2
Application number	US-202016806027-A
Country	US
Kind code	B2
Filing date	Mar 2, 2020
Priority date	Feb 25, 2011
Publication date	Aug 8, 2023
Grant date	Aug 8, 2023

Abstract

The present invention demonstrated that the modification of the Fc region of an antigen-binding molecule into an Fc region that does not form in a neutral pH range a heterotetramer complex containing two molecules of FcRn and an active Fcγ receptor improved the pharmacokinetics of the antigen-binding molecule and reduced the immune response to the antigen-binding molecule. The present invention also revealed methods for producing antigen-binding molecules having the properties described above, and successfully demonstrated that pharmaceutical compositions containing as an active ingredient such an antigen-binding molecule or an antigen-binding molecule produced by a production method of the present invention have excellent features over conventional antigen-binding molecules in that when administered, they exhibit improved pharmacokinetics and reduced in vivo immune response.

First claim

The invention claimed is:

1. A method for improving pharmacokinetics of an antigen-binding molecule, the method comprising:
identifying a first antigen-binding molecule comprising (a) an antigen-binding domain whose antigen-binding activity varies depending on pH or on calcium ion concentration, and (b) an Fc region that has FcRn-binding activity at pH 7.0;
producing a second antigen-binding molecule that is identical to the first antigen-binding molecule except for at least one amino acid mutation in the Fc region, wherein the ability of the second antigen-binding molecule to form a heterocomplex with two molecules of FcRn and one molecule of an activating Fcγ receptor at pH 7.4 is reduced compared to the ability of the first antigen-binding molecule to form such a heterocomplex at pH 7.4; and
conducting one or more assays to confirm that the second antigen-binding molecule has one or both of the following properties:
(1) increased plasma retention compared to the first antigen-binding molecule,
(2) decreased plasma clearance compared to the first antigen-binding molecule;

wherein the second antigen-binding molecule's ability to bind to the activating Fcγ receptor is decreased compared to the ability of an Fc region of a native human IgG to bind to the activating Fcγ receptor, and wherein the at least one amino acid mutation in the Fc region of the second antigen-binding molecule comprises substitution at one or more of the following EU numbering positions with an amino acid indicated below for each position:
Ala, Arg, Asn, Asp, Gln, Glu, Gly, His, Lys, Met, Phe, Pro, Ser, Thr, or Trp at position 234;
Ala, Asn, Asp, Gln, Glu, Gly, His, Ile, Lys, Met, Pro, Ser, Thr, Val, or Arg at position 235;
Arg, Asn, Gln, His, Leu, Lys, Met, Phe, Pro, or Tyr at position 236;
Ala, Asn, Asp, Gln, Glu, His, Ile, Leu, Lys, Met, Pro, Ser, Thr, Val, Tyr, or Arg at position 237;
Ala, Asn, Gln, Glu, Gly, His, Ile, Lys, Thr, Trp, or Arg at position 238;
Gln, His, Lys, Phe, Pro, Trp, Tyr, or Arg at position 239;
Ala, Arg, Asn, Gln, Gly, His, Ile, Leu, Lys, Met, Phe, Ser, Thr, Trp, Tyr, or Val at position 265;
Ala, Arg, Asn, Asp, Gln, Glu, Gly, His, Lys, Phe, Pro, Ser, Thr, Trp, or Tyr at position 266;
Arg, His, Lys, Phe, Pro, Trp, or Tyr at position 267;
Ala, Arg, Asn, Gln, Gly, His, Ile, Leu, Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, or Val at position 269;
Ala, Arg, Asn, Gln, Gly, His, Ile, Leu, Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, or Val at position 270;
Arg, His, Phe, Ser, Thr, Trp, or Tyr at position 271;
Arg, Asn, Asp, Gly, His, Phe, Ser, Trp, or Tyr at position 295;
Arg, Gly, Lys, or Pro at position 296;
Ala at position 297;
Arg, Gly, Lys, Pro, Trp, or Tyr at position 298;
Arg, Lys, or Pro at position 300;
Lys or Pro at position 324;
Ala, Arg, Gly, His, Ile, Lys, Phe, Pro, Thr, Trp, Tyr, or Val at position 325;
Arg, Gln, His, Ile, Leu, Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, or Val at position 327;
Arg, Asn, Gly, His, Lys, or Pro at position 328;
Asn, Asp, Gln, Glu, Gly, His, Ile, Leu, Lys, Met, Phe, Ser, Thr, Trp, Tyr, Val, or Arg at position 329;
Pro or Ser at position 330;
Arg, Gly, or Lys at position 331;
Arg, Lys, or Pro at position 332.

2. The method of claim 1 , wherein the activating Fcγ receptor is human FcγRIa, human FcγRIIa(R), human FcγRIIa(H), human FcγRIIIa(V), or human FcγRIIIa(F).

3. The method of claim 1 , wherein at least one of the following EU numbering positions in the Fc region of the first antigen-binding molecule and in the Fc region of the second antigen-binding molecule is occupied by one of the amino acid residues indicated below for each position:
Met at position 237;
Ile at position 248;
Ala, Phe, Ile, Met, Gln, Ser, Val, Trp, or Tyr at position 250;
Phe, Trp, or Tyr at position 252;
Thr at position 254;
Glu at position 255;
Asn, Asp, Glu, or Gln at position 256;
Ala, Gly, Ile, Leu, Met, Asn, Ser, Thr, or Val at position 257;
His at position 258;
Ala at position 265;
Ala or Glu at position 286;
His at position 289;
Ala at position 297;
Gly at position 298;
Ala at position 303;
Ala at position 305;
Ala, Asp, Phe, Gly, His, Ile, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Val, Trp, or Tyr at position 307;
Ala, Phe, Ile, Leu, Met, Pro, Gln, or Thr at position 308;
Ala, Asp, Glu, Pro, or Arg at position 309;
Ala, His, or Ile at position 311;
Ala or His at position 312;
Lys or Arg at position 314;
Ala, Asp, or His at position 315;
Ala at position 317;
Val at position 332;
Leu at position 334;
His at position 360;
Ala at position 376;
Ala at position 380;
Ala at position 382;
Ala at position 384;
Asp or His at position 385;
Pro at position 386;
Glu at position 387;
Ala or Ser at position 389;
Ala at position 424;
Ala, Asp, Phe, Gly, His, Ile, Lys, Leu, Asn, Pro, Gln, Ser, Thr, Val, Trp, or Tyr at position 428;
Lys at position 433;
Ala, Phe, His, Ser, Trp, or Tyr at position 434;
His, Ile, Leu, Phe, Thr, or Val at position 436.

4. The method of claim 1 , wherein the first and second antigen-binding molecules are antibodies.

5. The method of claim 1 , comprising assaying the second antigen-binding molecule's ability to form the heterocomplex at pH 7.4.

6. The method of claim 1 , comprising assaying the second antigen-binding molecule's ability to bind to the activating Fcγ receptor and thereby determining that the second antigen-binding molecule's ability to bind to the activating Fcγ receptor is decreased compared to the ability of the first antigen-binding molecule to bind to the activating Fcγ receptor.

7. A method for improving pharmacokinetics of an antigen-binding molecule, the method comprising:
identifying a first antigen-binding molecule comprising (a) an antigen-binding domain whose antigen-binding activity varies depending on pH or on calcium ion concentration, and (b) an Fc region that has FcRn-binding activity at pH 7.0;
producing a second antigen-binding molecule that is identical to the first antigen-binding molecule except for at least one amino acid mutation in the Fc region, wherein the ability of the second antigen-binding molecule to form a heterocomplex with two molecules of FcRn and one molecule of an activating Fcγ receptor at pH 7.4 is reduced compared to the ability of the first antigen-binding molecule to form such a heterocomplex at pH 7.4, wherein the second antigen-binding molecule has higher binding affinity to an inhibitory Fcγ receptor than to the activating Fcγ receptor, and wherein the at least one amino acid mutation in the Fc region of the second antigen-binding molecule comprises substitution of the amino acid at EU numbering position 238 with Asp and/or the amino acid at EU numbering position 328 with Glu; and
conducting one or more assays to confirm that the second antigen-binding molecule has one or both of the following properties:
(1) increased plasma retention compared to the first antigen-binding molecule,
(2) decreased plasma clearance compared to the first antigen-binding molecule.

8. The method of claim 7 , wherein the inhibitory Fcγ receptor is human FcγRIIb, and the activating Fcγ receptor is human FcγRIa, human FcγRIIa(R), human FcγRIIa(H), human FcγRIIIa(V), or human FcγRIIIa(F).

9. The method of claim 7 , wherein the at least one amino acid mutation in the Fc region of the second antigen-binding molecule comprises substitution of the amino acid at EU numbering position 238 with Asp and substitution of the amino acid at one or more of the following EU numbering positions with an amino acid residue indicated below for that position:
Asp at position 233;
Trp or Tyr at position 234;
Ala, Asp, Glu, Leu, Met, Phe, Trp, or Tyr at position 237;
Asp at position

Assignees

• Chugai Pharmaceutical Co Ltd

Inventors

• Igawa Tomoyuki
• Maeda Atsuhiko
• Haraya Kenta
• Iwayanagi Yuki
• Tachibana Tatsuhiko
• Mimoto Futa
• Kuramochi Taichi
• Katada Hitoshi
• Kadono Shojiro

Classifications

• C07K16/2866 Primary

  against receptors for cytokines, lymphokines, interferons · CPC title

• C07K16/08 Primary

  against material from viruses · CPC title

• C07K16/18

  against material from animals or humans · CPC title

• C07K16/303

  Liver or Pancreas · CPC title

• C07K2317/524

  CH2 domain · CPC title