Methods of making and using multispecific antibody panels and antibody analog panels

Patent metadata

Field	Value
Publication number	US-10584181-B2
Application number	US-201013510145-A
Country	US
Kind code	B2
Filing date	Dec 3, 2010
Priority date	Dec 4, 2009
Publication date	Mar 10, 2020
Grant date	Mar 10, 2020

Abstract

Multispecific antibodies that specifically bind at least two different epitopes are provided. Structural variants of native antibodies (antibody analogs) are also provided. Also provided are multispecific antibodies and antibody analogs having a range of biological activities. Agonist and antagonist multispecific antibodies and agonist and antagonist antibody analogs are provided. Multispecific antibodies and antibody analogs conjugated with therapeutic and/or diagnostic agents are also provided, as are multispecific antibodies and antibody analogs conjugated with agents to increase in vivo half-life compared to multispecific antibodies and antibody analogs lacking such agents. In addition, methods of making multispecific antibodies and antibody analogs and compositions comprising multispecific antibodies and antibody analogs are provided. Therapeutic, research, and diagnostic uses of multispecific antibodies and antibody analogs are also provided.

First claim

We claim:

1. A method of synthesizing a panel of multispecific antibodies, the method comprising:
(i)obtaining a first antigen binding fragment from a first parent antibody having a first monospecificity and a free sulfhydryl group;
(ii)reacting the first antigen binding fragment with a thio-reactive crosslinker to produce an antigen binding fragment-crosslinker moiety; and
(iii) reacting the antigen binding fragment-crosslinker moiety in different reaction mixtures with each of three or more additional antigen binding fragments obtained from one or more parent antibodies of different monospecificity from the first antigen binding fragment,
wherein each of the three or more additional antigen binding fragments has a single free sulfhydryl group, and
wherein the single free sulfhydryl groups of the additional antigen binding fragments are located at least at three different amino acid positions from each other,

thereby synthesizing the panel of isolated multispecific antibodies,
wherein each multispecific antibody of the panel if isolated multispecific antibodies comprises the first antigen binding fragment crosslinked to the additional antigen binding fragment via single free sulfhydryl group pairs selected from the group consisting of:
(a) position 110 of the light chain and position 110 of the light chain;
(b) position 110 of the light chain and position 205 of the light chain;
(c) position 110 of the light chain and position 118 of the heavy chain;
(d) position 110 of the light chain and position 121 of the heavy chain;
(e) position 110 of the light chain and a position in a hinge region;
(f) position 205 of the light chain and position 205 of the light chain;
(g) position 205 of the light chain and position 118 of the heavy chain;
(h) position 205 of the light chain and position 121 of the heavy chain;
(i) position 205 of the light chain and position in the hinge region;
(j) position 118 of the heavy chain and position 118 of the heavy chain;
(k) position 118 of the heavy chain and position 121 of the heavy chain;
(l) position 118 of the heavy chain and a position in the hinge region;
(m) position 121 of the heavy chain and position 121 of the heavy chain;
(n) position 121 of the heavy chain and a position in the hinge region; and
(o) a position in the hinge region and a position in the hinge region,
wherein the numbering of the residues is according to the EU numbering system, and

wherein the first antigen binding fragment and the additional antigen binding fragments each comprise 6 CDRs.

2. The method of claim 1 , wherein the first parent antibody is selected from the group consisting of an anti-Her1 antibody, an anti-Her2 antibody, an anti-FcεRIα antibody and anti-FcγRIIb antibody.

3. The method of claim 2 , wherein the first antigen binding fragment is obtained from an anti-Her2 antibody and each of the two or more additional antigen binding fragments is obtained from anti-Her1 antibody, or the first antigen binding fragment is obtained from anti-Her1 antibody and each of the three more additional antigen binding fragments is obtained from anti-Her2 antibody, or the first antigen binding fragment is obtained from an anti-FcεRIα antibody and each of the three or more additional antibgen binding fragments is obtained from an anti-FcγRIIb antibody, or the first antigen binding fragment is obtained from anti-FcγRIIb antibody and each of the three or more additional antigen binding fragments is obtained from anti-FcεRIα antibody.

4. The method of claim 2 , wherein the first parent antibody is an anti-Her2 antibody and is selected from the group consisting of trastuzumab and pertuzumab.

5. The method of claim 2 , wherein the first parent antibody is an anti-Her1 antibody and is selected from the group consisting of D1-5 and C3-101.

6. The method of claim 1 , wherein the first antigen binding fragment is obtained from an anti-Her2 antibody and the additional antigen binding fragments are obtained from an anti-Her1 antibody, and wherein the anti-Her2 antibody is trastuzumab or pertuzuamb and the anti-Her1 antibody is D1-5 or C3-101.

7. The method of claim 2 , wherein the anti-FcγRIIb antibody is 5A6.

8. The method of claim 2 , wherein the anti-FcεRIαantibody is 22E7.

9. The method of claim 3 , wherein the anti-FcγRIIb antibody is 5A6 and the anti-FcεRIα antibody is 22E7.

10. The method of claim 1 , wherein the thio-reactive crosslinker is selected from bis-maleimide, bis-alkyl halides, pyridyl disulfides, bis-mercurial salts, and bis-thiosulfonates.

11. The method of claim 10 , wherein the thio-reactive crosslinker is bis-maleimide.

12. The method of claim 1 , wherein the first antigen binding fragment or each of the three or more additional antigen fragments are obtained from a cysteine-engineered antibody.

13. The method of claim 12 , wherein the cysteine-engineered antibody comprises a substitution at position 110 or at position 205 of the light chain, wherein the numbering of the residues is according to the EU numbering system, and wherein the substitution is cysteine.

14. The method of claim 12 , wherein the cysteine-engineered antibody comprises a substitution at position 118 or at position 121 of the heavy chain, wherein the numbering of the residues is according to the EU numbering system, and wherein the substitution is cysteine.

15. A method of synthesizing a panel of antibody analogs, the method comprising:
(i) reacting a first antigen binding fragment having a free sulfhydryl group with a thio-reactive crosslinker to produce an antigen binding fragment-crosslinker moiety, and
(ii) reacting the antigen binding fragment-crosslinker moiety in different reaction mixtures with each of two or more additional antigen fragments,
wherein each of the two or more additional antigen binding fragments has a single free sulfhydryl group, and
wherein the single free sulfhydryl groups of each of the additional antigen binding fragments are located at least at two different amino acid positions from each other,

thereby synthesizing the panel of isolated antibody analogs,
wherein each of the first antigen binding fragment and the additional antigen binding fragments have the same monospecificity,
wherein each antibody analog of the panel of isolated antibody analogs comprises the first antigen binding fragment crosslinked to the additional antigen binding fragment via single free sulfhydryl group pairs selected from the group consisting of:
(a) position 110 of the light chain and position 110 of the light chain;
(b) position 110 of the light chain and position 205 of the light chain;
(c) position 110 of the light chain and position 118 of the heavy chain;
(d) position 110 of the light chain and position 121 of the heavy chain;
(e) position 110 of the light chain and a position in a hinge region;
(f) position 205 of the light chain and position 205 of the light chain;
(g) position 205 of the light chain and position 118 of the heavy chain;
(h) position 205 of the light chain and position 121 of the heavy chain;
(i) position 205 of the light chain and a position in a hinge region;
(j) position 118 of the heavy chain and position 118 of the heavy chain;
(k) position 118 of the heavy chain and position 121 of the heavy chain;
(l) position 118 of the heavy chain and a position in a hinge region;
(m) position 121 of the heavy chain and position 121 of the heavy chain;
(n) position 121 of the heavy chain and a position in a hinge region; and
(o) a position in the hinge region and a position in the hinge region,
wherein the numbering of the residues is accordi

Assignees

• Scheer Justin
• Vandlen Richard L
• Genentech Inc

Inventors

• Scheer Justin
• Vandlen Richard L

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• C07K2317/90

  characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin · CPC title

• C07K2317/76

  Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title

• C07K2317/73

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

• C07K2317/75

  Agonist effect on antigen · CPC title