Trivalent, bispecific antibodies

Abstract

The present invention relates to trivalent, bispecific antibodies, methods for their production, pharmaceutical compositions containing the antibodies, and uses thereof.

1 - 17 . (canceled) 
     
     
         18 : A method for treating a human suffering from cancer by administering an effective amount of trivalent, bispecific antibody to a human in need of such treatment, wherein the trivalent, bispecific antibody comprises
 a) a full length antibody that specifically binds to a first antigen wherein the full length antibody consists of two antibody heavy chains and two antibody light chains;   b) a polypeptide consisting of
 ba) an antibody heavy chain variable domain (VH), or 
 bb) an antibody heavy chain variable domain (VH) and an antibody constant domain 1 (CH1), 
 wherein the N-terminus of the VH domain of the polypeptide is fused via a peptide connector to the C-terminus of one of the two heavy chains of the full length antibody; 
   c) a polypeptide consisting of
 ca) an antibody light chain variable domain (VL), or 
 cb) an antibody light chain variable domain (VL) and an antibody light chain constant domain (CL); 
 wherein N-terminus of the VL domain of the polypeptide is fused via a peptide connector to the C-terminus of the other of the two heavy chains of the full length antibody; 
   
       and wherein the antibody heavy chain variable domain (VH) of the polypeptide under b) and the antibody light chain variable domain (VL) of the polypeptide under c) together form an antigen-binding site specifically binding to a second antigen. 
     
     
         19 : The method of  claim 18 , wherein
 the CH3 domain of one heavy chain and the CH3 domain of the other heavy chain of the trivalent, bispecific antibody each meet at an interface which comprises an alteration in the original interface between the antibody CH3 domains; wherein   i) in the CH3 domain of one heavy chain an amino acid residue is replaced with an amino acid residue having a larger side chain volume, thereby generating a protuberance within the interface of the CH3 domain of one heavy chain which is positionable in a cavity within the interface of the CH3 domain of the other heavy chain; and wherein   ii) in the CH3 domain of the other heavy chain   
       an amino acid residue is replaced with an amino acid residue having a smaller side chain volume, thereby generating a cavity within the interface of the second CH3 domain within which a protuberance within the interface of the first CH3 domain is positionable. 
     
     
         20 : The method of  claim 19 , wherein
 in i) the amino acid residue having a larger side chain volume is selected from the group consisting of arginine (R), phenylalanine (F), tyrosine (Y), tryptophan (W); and   in ii) the amino acid residue having a smaller side chain volume is selected from the group consisting of alanine (A), serine (S), threonine (T), valine (V).   
     
     
         21 : The method of  claim 20 , wherein both CH3 domains are further altered by the introduction of cysteine as an amino acid in each CH3 domain such that a disulfide bridge between both CH3 domains can be formed. 
     
     
         22 : The method of  claim 19 , wherein
 the CH3 domain under i) comprises a T366W mutation; and   
       the CH3 domain under ii) comprises T366S, L368A, and Y407V mutations. 
     
     
         23 : The method of  claim 19 , wherein
 the CH3 domain under i) comprises Y349C and T366W mutations; and   the CH3 domain under ii) comprises S354C, T366S, L368A, and Y407V mutations.   
     
     
         24 : The method of  claim 18 , wherein
 the antibody heavy chain variable domain (VH) of the polypeptide under b) and the antibody light chain variable domain (VL) of the polypeptide under c) are linked and stabilized via a interchain disulfide bridge by introduction of a disulfide bond between the following positions:   i) heavy chain variable domain position 44 to light chain variable domain position 100,   ii) heavy chain variable domain position 105 to light chain variable domain position 43, or   iii) heavy chain variable domain position 101 to light chain variable domain position 100.   
     
     
         25 : The method of  claim 18 , wherein
 the antibody heavy chain variable domain (VH) of the polypeptide under b) and the antibody light chain variable domain (VL) of the polypeptide under c) are linked and stabilized via a interchain disulfide bridge by introduction of a disulfide bond between the following positions: i) heavy chain variable domain position 44 to light chain variable domain position 100.   
     
     
         26 : The method of  claim 18 , wherein the peptide connectors under b) and c) are identical peptides with a length between 25 and 50 amino acids.