Humanization of rabbit antibodies using a universal antibody framework
The present invention relates to an universal antibody acceptor framework and to methods for grafting non-human antibodies, e.g., rabbit antibodies, using a universal antibody acceptor framework. Antibodies generated by the methods of the invention are useful in a variety of diagnostic and therapeutic applications.
1. An immunobinder comprising:
(i) a light chain variable domain comprising human light chain framework sequences that are at least 85% identical to the light chain framework sequences of SEQ ID NO: 2; and
(ii) a heavy chain variable domain comprising human heavy chain framework sequences that are at least 85% identical to the heavy chain framework sequences of SEQ ID NO: 4 and comprises a threonine (T) at position 24 according to AHo numbering;
wherein the CDR1, CDR2, and CDR3 polypeptide sequences of the light chain variable domain of (i) are substituted with the light chain CDR1, CDR2, and CDR3 from a donor rabbit immunobinder and the CDR1, CDR2, and CDR3 polypeptide sequences of the heavy chain variable domain of (ii) are substituted with the heavy chain CDR1, CDR2, and CDR3 from a donor rabbit immunobinder.
2. The immunobinder of claim 1 , wherein the amino acid sequence of the heavy chain variable domain comprises glycine (G) at position 56, threonine (T) at position 84, valine (V) at position 89, and arginine (R) at position 108 according to AHo numbering.
3. The immunobinder of claim 1 , wherein said heavy chain variable domain comprises glycine (G) at position 56 according to AHo numbering.
4. The immunobinder of claim 1 , wherein said heavy chain variable domain comprises threonine (T) at position 84 according to AHo numbering.
5. The immunobinder of claim 1 , wherein said heavy chain variable domain comprises valine (V) at position 89 according to AHo numbering.
6. The immunobinder of claim 1 , wherein said heavy chain variable domain comprises arginine (R) at position 108 according to AHo numbering.
7. The immunobinder of claim 1 , wherein said heavy chain variable domain further comprises at least one of the following amino acids: Serine (S) at position 12; Serine (S) or Threonine (T) at position 103; and Serine (S) or Threonine (T) at position 144 according to AHo numbering.
8. The immunobinder of claim 1 , wherein said heavy chain variable domain further comprises Glycine (G) at position 141 according to AHo numbering.
9. The immunobinder of claim 1 , wherein said light chain variable domain comprises threonine (T) at position 87 according to AHo numbering.
10. The immunobinder of claim 1 , wherein said heavy chain variable domain and said light chain variable domain are linked via a linker sequence that comprises SEQ ID NO: 8.
11. The immunobinder of claim 1 comprising an amino acid sequence that is at least 85% identical to SEQ ID NO: 3, SEQ ID NO: 5, or SEQ ID NO: 7.
12. The immunobinder of claim 1 , wherein said light chain variable domain further comprises at least one of the following amino acids: glutamic acid (E) at position 1, valine (V) at position 3, leucine (L) at position 4, Serine (S) at position 10, Arginine (R) at position 47, Serine (S) at position 57, phenylalanine (F) at position 91, and Valine (V) at position 103 according to AHo numbering.
13. The immunobinder of claim 1 , wherein said heavy chain variable domain further comprises a valine (V) at position 25 and/or a lysine (K) at position 82 according to AHo numbering.
14. The immunobinder of claim 1 , wherein said immunobinder is an scFv.
15. A pharmaceutical composition comprising the immunobinder of claim 1 and a pharmaceutically acceptable excipient.
16. A bispecific molecule comprising the immunobinder of claim 1 .
17. The bispecific molecule of claim 16 , which binds to at least two different binding sites or target molecules.
18. The bispecific molecule of claim 16 , wherein the immunobinder is linked to an antibody, an antibody fragment, a Fab, a Fab′, a F(ab′) 2 , a Fv or a single chain Fv, tumor specific or pathogen specific antigens, a peptide or a binding mimetic.
19. A method for making an immunobinder, the immunobinder comprising rabbit heavy chain CDR H1, CDR H2 and CDR H3 sequences and light chain CDR L1, CDR L2 and CDR L3 sequences, the method comprising:
(i) grafting the rabbit CDR H1, CDR H2 and CDR H3 sequences into a heavy chain variable domain that comprises human heavy chain framework sequences that are at least 85% identical to the heavy chain framework sequences of SEQ ID NO: 4, and that comprises a threonine (T) at position 24 according to AHo numbering, and
(ii) grafting the rabbit CDR L1, CDR L2 and CDR L3 sequences into a light chain variable domain that comprises human light chain framework sequences that are at least 85% identical to the light chain framework sequences of SEQ ID NO: 2.