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US 11,447,575 B2Granted
Bispecific antibody platform
AssigneeBiogen MA Inc.
InventorMartin Preyer
Life of this patent
Estimating the term…
Abstract
Provided herein is a platform technology for the generation of properly paired bispecific antibodies. Some of the antibodies generated have Fc region modifications, in particular in their CH3 domains by lysine repositioning to drive heterodimerization of the two heavy chains of the bispecific antibody. Some of the antibodies generated have Fab arm modifications to prevent mispairing of light chains. Specifically, the CH1 and CL domains of one of the Fab arms of the bispecific antibody are substituted with an IgE CH2 domain or an IgM CH2 domain.
Claims25
A tetravalent bispecific antibody comprising:
- (i) a first Fab and a second Fab,
- wherein the first Fab comprises a first heavy chain variable domain (first VH) and a first light chain variable domain (first VL), wherein the first VH and the first VL pair to form a first variable region that binds specifically to a first epitope of a first antigen, and
- wherein the second Fab comprises a second heavy chain variable domain (second VH) and a second light chain variable domain (second VL), wherein the second VH and the second VL pair to form a second variable region that binds specifically to the first epitope of the first antigen;
- and
- (ii) a whole antibody comprising a first heavy chain comprising a first hinge, a first IgG CH2 domain, a first IgG CH3 domain, and a third VH, a second heavy chain comprising a second hinge, a second IgG CH2 domain, a second IgG CH3 domain, and a fourth VH, a first light chain comprising a third VL, and a second light chain comprising a fourth VL, wherein the third VH and the third VL pair to form a third variable region that binds specifically to a first epitope of a second antigen, and wherein the fourth VH and the fourth VL pair to form a fourth variable region that binds specifically to the first epitope of the second antigen,
- wherein the third VH is either directly linked or linked via a linker of 1 to 25 amino acids to a first polypeptide, the third VL is either directly linked or linked via a linker of 1 to 25 amino acids to a second polypeptide, the fourth VH is either directly linked or linked via a linker of 1 to 25 amino acids to a third polypeptide, and the fourth VL is either directly linked or linked via a linker of 1 to 25 amino acids to a fourth polypeptide;
- wherein the first, second, third, and fourth polypeptides each comprise:
- (a) an amino acid sequence that is identical to amino acids 9-107 of the amino acid sequence of the CH2 domain of human immunoglobulin E (IgE) (SEQ ID NO:1);
- (b) an amino acid sequence that is identical to amino acids 9-107 of SEQ ID NO:1 with an N43Q mutation;
- (c) an amino acid sequence that is identical to amino acids 9-107 of SEQ ID NO:1 with a T45A or T45C mutation;
- (d) an amino acid sequence that is identical to amino acids 9-107 of SEQ ID NO:1 with an S17I or S17T mutation;
- or
- (e) an amino acid sequence that is identical to amino acids 9-107 of SEQ ID NO:1 with a T103G or T103S mutation,
- wherein the numbering of the amino acid positions in (a) to (e) is according to SEQ ID NO:1;
- or wherein
- (f) the first and third polypeptides each comprise an amino acid sequence that is identical to amino acids 6-104 of SEQ ID NO:3, and the second and fourth polypeptides each comprise an amino acid sequence that is identical to amino acids 6-104 of SEQ ID NO:4;
- (g) the first and third polypeptides each comprise an amino acid sequence that is identical to amino acids 6-104 of SEQ ID NO:47, and the second and fourth polypeptides each comprise an amino acid sequence that is identical to amino acids 6-104 of SEQ ID NO:48;
- (h) the first and third polypeptides each comprise an amino acid sequence that is identical to amino acids 6-104 of SEQ ID NO:49, and the second and fourth polypeptides each comprise an amino acid sequence that is identical to amino acids 6-104 of SEQ ID NO:50;
- or
- (i) the first and third polypeptides each comprise an amino acid sequence that is identical to amino acids 6-104 of SEQ ID NO:5, and the second and fourth polypeptides each comprise an amino acid sequence that is identical to amino acids 6-104 of SEQ ID NO:6;
- and
- wherein the first polypeptide is either directly linked or linked via a linker of 1 to 25 amino acids to the N-terminus of the first hinge and the third polypeptide is either directly linked or linked via a linker of 1 to 25 amino acids to the N-terminus of the second hinge;
- and
- wherein the first Fab is connected to the C-terminus of the first IgG CH3 domain and the second Fab is connected to the C-terminus of the second IgG CH3 domain.
21 more elements
A tetravalent bispecific antibody comprising:
- (i) a first Fab and a second Fab,
- wherein the first Fab comprises a first heavy chain variable domain (first VH) and a first light chain variable domain (first VL), wherein the first VH and the first VL pair to form a first variable region that binds specifically to a first epitope of a first antigen, and
- wherein the second Fab comprises a second heavy chain variable domain (second VH) and a second light chain variable domain (second VL), wherein the second VH and the second VL pair to form a second variable region that binds specifically to the first epitope of the first antigen;
- and
- (ii) a whole antibody comprising a first heavy chain comprising a first hinge, a first IgG CH2 domain, a first IgG CH3 domain, and a third VH, a second heavy chain comprising a second hinge, a second IgG CH2 domain, a second IgG CH3 domain, and a fourth VH, a first light chain comprising a third VL, and a second light chain comprising a fourth VL, wherein the third VH and the third VL pair to form a third variable region that binds specifically to a first epitope of a second antigen, and wherein the fourth VH and the fourth VL pair to form a fourth variable region that binds specifically to the first epitope of the second antigen,
- wherein the third VH is either directly linked or linked via a linker of 1 to 25 amino acids to a first polypeptide, the third VL is either directly linked or linked via a linker of 1 to 25 amino acids to a second polypeptide, the fourth VH is either directly linked or linked via a linker of 1 to 25 amino acids to a third polypeptide, and the fourth VL is either directly linked or linked via a linker of 1 to 25 amino acids to a fourth polypeptide;
- wherein the first, second, third, and fourth polypeptides each comprise
- (a) an amino acid sequence that is identical to amino acids 7-112 of the amino acid sequence of the CH2 domain of human immunoglobulin M (IgM) (SEQ ID NO:2;
- (b) an amino acid sequence that is identical to amino acids 7-112 of SEQ ID NO:2 with an N105Q mutation;
- (c) an amino acid sequence that is identical to amino acids 7-112 of SEQ ID NO:2 with an S107A or S107C mutation;
- (d) an amino acid sequence that is identical to amino acids 7-110 of SEQ ID NO:2;
- (e) an amino acid sequence that is identical to amino acids 7-110 of SEQ ID NO:2 with an N105Q mutation;
- or
- (f) an amino acid sequence that is identical to amino acids 7-110 of SEQ ID NO:2 with an S107A or S107C mutation,
- wherein the numbering of the amino acid positions in (a) to (f) is according to SEQ ID NO:2;
- wherein the first polypeptide is either directly linked or linked via a linker of 1 to 25 amino acids to the N-terminus of the first hinge and the third polypeptide is either directly linked or linked via a linker of 1 to 25 amino acids to the N-terminus of the second hinge;
- and
- wherein the first Fab is connected to the C-terminus of the first IgG CH3 domain and the second Fab is connected to the C-terminus of the second IgG CH3 domain.
15 more elements
Dependencies are inferred from the claim text.