Anti-CD38 antibodies and fusions to attenuated interferon alpha-2B
Antibodies that specifically bind to CD38, as well as constructs comprising such antibodies fused to attenuated interferon alpha-2B proteins are provided. Anti-CD38-attenuated interferon alpha-2b fusion constructs may be used to inhibit proliferation in cancerous cells that express both CD38 and the receptor for IFN-alpha2b, as well as to induce apoptosis in such cells. Inhibition of proliferation and induction of apoptosis in cancerous cells may serve as the basis for the treatment of the underlying cancer.
1. A recombinant antibody, comprising the heavy chain complementarity determining region 1 (CDR1), CDR2, and CDR3 of SEQ ID NO: 665 and the light chain CDR1, CDR2, and CDR3 of SEQ ID NO: 666, wherein the antibody specifically binds to CD38.
2. The recombinant antibody according to claim 1 , wherein the antibody is a humanized antibody.
3. The recombinant antibody according to claim 1 , wherein the antibody comprises a human IgG1 heavy chain constant region.
4. The recombinant antibody according to claim 1 , wherein the antibody comprises a human IgG4 heavy chain constant region.
5. The recombinant antibody according to claim 4 , wherein the human IgG4 heavy chain constant region comprises a proline at position 228 according to the EU numbering system.
6. The recombinant antibody according to claim 1 , wherein the antibody further is fused to an attenuated human interferon alpha 2b.
7. The recombinant antibody according to claim 6 , wherein the attenuated human interferon alpha 2b comprises an alanine to aspartic acid substitution at position 145 relative to the amino acid sequence of SEQ ID NO: 648.
8. The recombinant antibody according to claim 6 , wherein the attenuated human interferon alpha 2b comprises the amino acid sequence of SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 650, or SEQ ID NO: 651.
9. The recombinant antibody according to claim 5 , wherein the antibody further is fused to an attenuated human interferon alpha 2b comprising an alanine to aspartic acid substitution at position 145 relative to the amino acid sequence of SEQ ID NO: 648.
10. A composition, comprising the recombinant antibody according to claim 1 and a pharmaceutically acceptable carrier.
11. A composition, comprising the recombinant antibody according to claim 9 and a pharmaceutically acceptable carrier.
12. The recombinant antibody according to claim 1 , wherein the heavy chain CDR1 comprises the amino acid sequence of SEQ ID NO: 514, the heavy chain CDR2 comprises the amino acid sequence of SEQ ID NO: 516, the heavy chain CDR3 comprises the amino acid sequence of SEQ ID NO: 518, the light chain CDR1 comprises the amino acid sequence of SEQ ID NO: 608, the light chain CDR2 comprises the amino acid sequence of SEQ ID NO: 591, and the light chain CDR3 comprises the amino acid sequence of SEQ ID NO: 612.
13. The recombinant antibody according to claim 12 , wherein the antibody comprises a human IgG4 heavy chain constant region, wherein the antibody further is fused to an attenuated human interferon alpha 2b comprising an alanine to aspartic acid substitution at position 145 relative to the amino acid sequence of SEQ ID NO: 648.
14. The recombinant antibody according to claim 13 , wherein the attenuated human interferon alpha 2b comprises the amino acid sequence of SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 650, or SEQ ID NO: 651.
15. The recombinant antibody according to claim 12 , wherein the antibody comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 156 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 185.
16. The recombinant antibody according to claim 15 , wherein the antibody comprises a human IgG4 heavy chain constant region.
17. The recombinant antibody according to claim 16 , wherein the antibody further is fused to an attenuated human interferon alpha 2b.
18. The recombinant antibody according to claim 17 , wherein the attenuated human interferon alpha 2b comprises an alanine to aspartic acid substitution at position 145 relative to the amino acid sequence of SEQ ID NO: 648.
19. A composition, comprising the recombinant antibody according to claim 13 and a pharmaceutically acceptable carrier.
20. A composition, comprising the recombinant antibody according to claim 17 and a pharmaceutically acceptable carrier.
21. A recombinant antibody, comprising a heavy chain variable region comprising a CDR1, CDR2, and CDR3, the heavy chain variable region comprising an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 156 and a light chain variable region comprising a CDR1, CDR2, and CDR3, the light chain variable region comprising an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 185, wherein any amino acid changes in the heavy chain variable region or light chain variable region are outside of the CDRs, and wherein the antibody specifically binds to CD38.
22. The recombinant antibody according to claim 21 , wherein the antibody further is fused to an attenuated human interferon alpha 2b comprising an alanine to aspartic acid substitution at position 145 relative to the amino acid sequence of SEQ ID NO: 648.
23. A composition, comprising the recombinant antibody according to claim 22 and a pharmaceutically acceptable carrier.
24. An anti-CD38 antibody-attenuated interferon alpha-2b fusion construct, comprising:
an antibody that specifically binds to CD38, wherein the antibody comprises the heavy chain CDR1, CDR2, and CDR3 of SEQ ID NO: 665 and the light chain CDR1, CDR2, and CDR3 of SEQ ID NO: 666, wherein the antibody specifically binds to CD38; and
an attenuated human interferon alpha-2b comprising an alanine to aspartic acid substitution at position 145 relative to the amino acid sequence of SEQ ID NO: 648.
25. The fusion construct according to claim 24 , wherein the heavy chain CDR1 comprises the amino acid sequence of SEQ ID NO: 514, the heavy chain CDR2 comprises the amino acid sequence of SEQ ID NO: 516, the heavy chain CDR3 comprises the amino acid sequence of SEQ ID NO: 518, the light chain CDR1 comprises the amino acid sequence of SEQ ID NO: 608, the light chain CDR2 comprises the amino acid sequence of SEQ ID NO: 591, and the light chain CDR3 comprises the amino acid sequence of SEQ ID NO: 612.
26. The fusion construct according to claim 25 , wherein the antibody comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 156 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 185.
27. A composition, comprising the fusion construct according to claim 26 and a pharmaceutically acceptable carrier.