CD80 variant immunomodulatory proteins and uses thereof
Provided herein are variant CD80 polypeptides, immunomodulatory proteins comprising variant CD80 polypeptides, and nucleic acids encoding such proteins. The immunomodulatory proteins provide therapeutic utility for a variety of immunological and oncological conditions. Compositions and methods for making and using such proteins are provided.
1. A purified homodimer comprising two copies of a CD80-Fc immunomodulatory protein of the formula CD80-linker-Fc, wherein:
CD80 is a variant CD80 polypeptide comprising an amino acid substitution at position 68 in an unmodified CD80 polypeptide set forth in SEQ ID NO:28 or a portion thereof comprising an IgV domain, wherein the amino acid substitution at position 68 is V68M or V68A, and wherein the variant CD80 polypeptides comprises a sequence of amino acids that exhibits at least 90% sequence identity to the sequence set forth in SEQ ID NO:28 or the portion of SEQ ID NO:28 comprising an IgV domain; and
the variant CD80 polypeptide specifically binds to the ectodomain of human PD-L1 with increased binding affinity compared to the binding of the unmodified CD80 polypeptide to the ectodomain of human PD-L1.
2. The purified homodimer of claim 1 , wherein the IgV domain is amino acids 35-135, 35-138, 37-138, or 35-141 of SEQ ID NO:1.
3. The purified homodimer of claim 1 , wherein the IgV domain is amino acids 35-141 of SEQ ID NO:1.
4. The purified homodimer of claim 1 , wherein the amino acid substitution at position 68 is the amino acid substitution V68M.
5. The purified homodimer of claim 1 , wherein the variant CD80 polypeptide comprises up to 10 amino acid substitutions.
6. The purified homodimer of claim 1 , wherein the Fc domain is a variant IgG1 Fc domain with reduced effector function.
7. The purified homodimer of claim 6 , wherein the variant Fc domain comprises the amino acid substitutions R292C/N297G/V302C.
8. The purified homodimer of claim 6 , wherein the variant Fc domain comprises the amino acid substitutions L234A/L235E/G237A.
9. A pharmaceutical composition, comprising the purified homodimer of claim 8 and a pharmaceutically acceptable excipient.
10. The purified homodimer of claim 1 , wherein the Fc domain is an Fc domain of IgG2.
11. The purified homodimer of claim 1 , wherein the Fc domain is an Fc domain of IgG4 or is a variant IgG4 Fc domain containing a S228P mutation.
12. A pharmaceutical composition, comprising the purified homodimer of claim 1 and a pharmaceutically acceptable excipient.
13. A purified homodimer comprising two copies of a CD80-Fc immunomodulatory protein of the formula CD80-linker-Fc, wherein:
CD80 is a variant CD80 polypeptide comprising a sequence of amino acids that exhibits at least 90% sequence identity to an unmodified CD80 polypeptide set forth as amino acids 35-141 of SEQ ID NO:1 and comprises an amino acid substitution at position 68 in the unmodified CD80 polypeptide, wherein the amino acid substitution at position 68 is V68M or V68A; and
the variant CD80 polypeptide specifically binds to the ectodomain of human PD-L1 with increased binding affinity compared to the binding of the unmodified CD80 polypeptide to the ectodomain of human PD-L1.
14. The purified homodimer of claim 13 , wherein the amino acid substitution at position 68 is the amino acid substitution V68M.
15. The purified homodimer of claim 13 , wherein the variant CD80 polypeptide comprises up to 10 amino acid substitutions.
16. The purified homodimer of claim 13 , wherein the Fc domain is a variant IgG1 Fc domain with reduced effector function.
17. A pharmaceutical composition, comprising the purified homodimer of claim 16 and a pharmaceutically acceptable excipient.
18. The purified homodimer of claim 16 , wherein the variant Fc domain comprises the amino acid substitutions R292C/N297G/V302C.
19. The purified homodimer of claim 16 , wherein the variant Fc domain is an IgG1 Fc domain comprising the amino acid substitutions L234A/L235E/G237A.
20. A pharmaceutical composition, comprising the purified homodimer of claim 19 and a pharmaceutically acceptable excipient.
21. The purified homodimer of claim 13 , wherein the Fc domain is an Fc domain of IgG2.
22. The purified homodimer of claim 13 , wherein the Fc domain is an Fc domain of IgG4 or is a variant IgG4 Fc domain containing a S228P mutation.
23. A pharmaceutical composition, comprising the purified homodimer of claim 22 and a pharmaceutically acceptable excipient.
24. A pharmaceutical composition, comprising the purified homodimer of claim 13 and a pharmaceutically acceptable excipient.