Immunoglobulin variable domains

Abstract

VH domain, in which: (i) the amino acid residue at position 112 is one of K or Q; and/or (ii) the amino acid residue at position 89 is T; and/or (iii) the amino acid residue at position 89 is L and the amino acid residue at position 110 is one of K or Q; and (iv) in each of cases (i) to (iii), the amino acid at position 11 is preferably V; and in which said VH domain contains a C-terminal extension (X)n, in which a is 1 to 10, preferably 1 to 5, such as 1, 2, 3, 4 or 5 (and preferably 1 or 2, such as 1); and each X is an (preferably naturally occurring) amino acid residue that is independently chosen, and preferably independently chosen from the group consisting of alanine (A), glycine (G), valine (V), leucine (L) or isoleucine (I).

The invention claimed is: 
     
         1 . A heavy chain immunoglobulin single variable domain (ISVD) in which the amino acid residue at Kabat position 11 is V and the amino acid residue at Kabat position 89 is L, wherein the heavy chain ISVD specifically binds to:
 (A) IL-23 and comprises:
 (i) a CDR1 sequence that is the sequence of SEQ ID NO: 173; a CDR2 sequence that is the sequence of SEQ ID NO: 174; and a CDR3 sequence that is the sequence of SEQ ID NO: 175; or 
 (ii) a CDR1 sequence that is the sequence of SEQ ID NO: 191; a CDR2 sequence that is the sequence of SEQ ID NO: 192; and a CDR3 sequence that is the sequence of SEQ ID NO: 193; 
 or 
   (B) TNF and comprises:
 a CDR1 sequence that is the sequence of SEQ ID NO: 335; a CDR2 sequence that is the sequence of SEQ ID NO: 336; and a CDR3 sequence that is the sequence of SEQ ID NO: 337. 
   
     
     
         2 . The heavy chain ISVD of  claim 1 , wherein:
 the amino acid residue at Kabat position 14 is selected from the group consisting of A and P;   the amino acid residue at Kabat position 41 is selected from the group consisting of A and P;   the amino acid residue at Kabat position 108 is selected from the group consisting of Q and L; and   the amino acid residue at Kabat position 110 is selected from the group consisting of T and Q.   
     
     
         3 . The heavy chain ISVD of  claim 1 , further comprising a C-terminal extension (X) n , in which n is 1 to 10, wherein each X is an independently chosen amino acid. 
     
     
         4 . The heavy chain ISVD of  claim 3 , wherein each X is an amino acid independently chosen from the group consisting of A, G, V, L, and I. 
     
     
         5 . The heavy chain ISVD of  claim 1 , wherein the C-terminal end of the heavy-chain ISVD comprises an amino acid sequence selected from the group consisting of: VTVSS (SEQ ID NO:76), VTVSS(X) n , (SEQ ID NO:77), VKVSS (SEQ ID NO: 95), VKVSS(X) n  (SEQ ID NO:97), VQVSS (SEQ ID NO: 96), VQVSS(X) n  (SEQ ID NO: 98), in which n is 1 to 10, wherein each X is an independently chosen amino acid. 
     
     
         6 . The heavy chain ISVD of  claim 5 , wherein each X is an amino acid independently chosen from the group consisting of A, G, V, L, and I. 
     
     
         7 . The heavy chain ISVD of  claim 1 , which is a VHH domain, a humanized VHH domain, or a camelized VH domain. 
     
     
         8 . A fusion polypeptide comprising a heavy chain ISVD according to  claim 1  fused to an additional heavy chain ISVD. 
     
     
         9 . The fusion polypeptide of  claim 8 , wherein the heavy chain ISVDs are linked directly or via a suitable linker. 
     
     
         10 . The fusion polypeptide of  claim 8 , wherein the additional heavy chain ISVD specifically binds to serum albumin. 
     
     
         11 . The fusion polypeptide of  claim 10 , wherein the additional heavy chain ISVD has at least 90% sequence identity with Alb-8 (SEQ ID NO:46) or Alb-23 (SEQ ID NO:61). 
     
     
         12 . The fusion polypeptide of  claim 10 , wherein the additional heavy chain ISVD comprises a CDR1, CDR2, and CDR3 in which: CDR1 comprises the amino acid sequence SFGMS (SEQ ID NO:41); CDR2 comprises the amino acid sequence SISGSGSDTLYADSVKG (SEQ ID NO:42); and CDR3 comprises the amino acid sequence GGSLSR (SEQ ID NO:43). 
     
     
         13 . A composition comprising a fusion polypeptide according to  claim 10 , further comprising at least one pharmaceutically acceptable carrier, diluent or excipient. 
     
     
       14. The heavy chain ISVD of  claim 1 , wherein the heavy chain ISVD specifically binds to IL-23 and comprises: a CDR1 sequence that is the sequence of SEQ ID NO: 173; a CDR2 sequence that is the sequence of SEQ ID NO: 174; and a CDR3 sequence that is the sequence of SEQ ID NO: 175.  
     
     
       15. The heavy chain ISVD of  claim 14 , wherein:
 the amino acid residue at Kabat position 14 is selected from the group consisting of A and P;   the amino acid residue at Kabat position 41 is selected from the group consisting of A and P;   the amino acid residue at Kabat position 108 is selected from the group consisting of Q and L; and   the amino acid residue at Kabat position 110 is selected from the group consisting of T and Q.    
     
     
       16. The heavy chain ISVD of  claim 1 , wherein the heavy chain ISVD specifically binds to IL-23 and comprises: a CDR1 sequence that is the sequence of SEQ ID NO: 191; a CDR2 sequence that is the sequence of SEQ ID NO: 192; and a CDR3 sequence that is the sequence of SEQ ID NO: 193.  
     
     
       17. The heavy chain ISVD of  claim 16 , wherein:
 the amino acid residue at Kabat position 14 is selected from the group consisting of A and P;   the amino acid residue at Kabat position 41 is selected from the group consisting of A and P;   the amino acid residue at Kabat position 108 is selected from the group consisting of Q and L; and   the amino acid residue at Kabat position 110 is selected from the group consisting of T and Q.    
     
     
       18. The heavy chain ISVD of  claim 1 , wherein the heavy chain ISVD specifically binds to TNF and comprises: a CDR1 sequence that is the sequence of SEQ ID NO: 335; a CDR2 sequence that is the sequence of SEQ ID NO: 336; and a CDR3 sequence that is the sequence of SEQ ID NO: 337.  
     
     
       19. The heavy chain ISVD of  claim 18 , wherein:
 the amino acid residue at Kabat position 14 is selected from the group consisting of A and P;   the amino acid residue at Kabat position 41 is selected from the group consisting of A and P;   the amino acid residue at Kabat position 108 is selected from the group consisting of Q and L; and   the amino acid residue at Kabat position 110 is selected from the group consisting of T and Q.