Heterodimeric Fc-fused proteins
The present invention provides Fc-fused protein constructs, which as monovalent dimers have a higher serum half-life compared to a native/natural molecule, and are, therefore, advantageous for achieving higher titers of the proteins during production, higher stability during storage, and improved efficacy when used as a therapeutic. Also provided are Fc-fused protein constructs having mutations in the Fc region that reduce effector functions, which have increased activity to inhibit tumor growth and are, therefore, advantageous when used as a cancer therapy.
1. A heterodimeric Fc-fused protein comprising:
(a) a first polypeptide comprising a first human IgG1 Fc domain polypeptide and a first subunit of a multisubunit protein,
wherein the first human IgG1 Fc domain polypeptide comprises CH3 domain substitutions Y349C, K360E, and K409W, numbered according to the EU numbering system,
wherein the first subunit of the multisubunit protein is a p40 subunit of human IL-12,
wherein the first polypeptide comprises a linker connecting the first human IgG1 Fc domain polypeptide and the first subunit of the multisubunit protein,
wherein the linker of the first polypeptide comprises amino acid sequence PKSSDKTHTCPPCPAPEAAGG (SEQ ID NO:239), and
wherein the first polypeptide comprises amino acid sequence SEQ ID NO:290; and
(b) a second polypeptide comprising a second human IgG1 Fc domain polypeptide and a second, different subunit of the multisubunit protein,
wherein the second human IgG1 Fc domain polypeptide comprises CH3 domain substitutions Q347R, D399V, F405T, and S354C, numbered according to the EU numbering system,
wherein the second, different subunit of the multisubunit protein is a p35 subunit of human IL-12,
wherein the second polypeptide comprises a linker connecting the second human IgG1 Fc domain polypeptide and the second, different subunit of the multisubunit protein,
wherein the linker of the second polypeptide comprises amino acid sequence
(SEQ ID NO: 10)
GGGGSGGGGSGGGGSEPKSSDKTHTCPPCPAPEAAGG;
and
wherein the second polypeptide comprises amino acid sequence SEQ ID NO:291;
wherein the first human IgG1 Fc domain polypeptide and the second human IgG1 Fc domain polypeptide each comprise CH2 domain substitutions L234A, L235A, and P329A, numbered according to the EU numbering system, and
wherein the first subunit and the second, different subunit of the multisubunit protein are bound to each other.
2. The heterodimeric Fc-fused protein of claim 1 , wherein
(a) the first polypeptide consists of amino acid sequence SEQ ID NO:290; and
(b) the second polypeptide consists of amino acid sequence SEQ ID NO:291.
3. The heterodimeric Fc-fused protein of claim 1 , wherein
the second polypeptide consists of amino acid sequence SEQ ID NO:291.
4. The heterodimeric Fc-fused protein of claim 1 , wherein
the first polypeptide consists of amino acid sequence SEQ ID NO:290.
5. A pharmaceutical composition comprising a heterodimeric Fc-fused protein and a pharmaceutically acceptable carrier, wherein the heterodimeric Fc-fused protein comprises:
(a) a first polypeptide comprising a first human IgG1 Fc domain polypeptide and a first subunit of a multisubunit protein,
wherein the first human IgG1 Fc domain polypeptide comprises CH3 domain substitutions Y349C, K360E, and K409W, numbered according to the EU numbering system,
wherein the first subunit of the multisubunit protein is a p40 subunit of human IL-12,
wherein the first polypeptide comprises a linker connecting the first human IgG1 Fc domain polypeptide and the first subunit of the multisubunit protein,
wherein the linker of the first polypeptide comprises amino acid sequence PKSSDKTHTCPPCPAPEAAGG (SEQ ID NO:239), and
wherein the first polypeptide comprises amino acid sequence SEQ ID NO:290; and
(b) a second polypeptide comprising a second human IgG1 Fc domain polypeptide and a second, different subunit of the multisubunit protein,
wherein the second human IgG1 Fc domain polypeptide comprises CH3 domain substitutions Q347R, D399V, F405T, and S354C, numbered according to the EU numbering system,
wherein the second, different subunit of the multisubunit protein is a p35 subunit of human IL-12,
wherein the second polypeptide comprises a linker connecting the second human IgG1 Fc domain polypeptide and the second, different subunit of the multisubunit protein,
wherein the linker of the second polypeptide comprises amino acid sequence
(SEQ ID NO: 10)
GGGGSGGGGSGGGGSEPKSSDKTHTCPPCPAPEAAGG;
and
wherein the second polypeptide comprises amino acid sequence SEQ ID NO:291;
wherein the first human IgG1 Fc domain polypeptide and the second human IgG1 Fc domain polypeptide each comprise CH2 domain substitutions L234A, L235A, and P329A, numbered according to the EU numbering system, and
wherein the first subunit and the second, different subunit of the multisubunit protein are bound to each other.
6. The pharmaceutical composition of claim 5 , wherein
(a) the first polypeptide consists of amino acid sequence SEQ ID NO:290; and
(b) the second polypeptide consists of amino acid sequence SEQ ID NO:291.
7. The pharmaceutical composition of claim 5 , wherein the composition is suitable for intravenous, subcutaneous, intraperitoneal, or intratumoral administration.
8. The pharmaceutical composition of claim 5 , wherein
the second polypeptide consists of amino acid sequence SEQ ID NO:291.
9. The pharmaceutical composition of claim 5 , wherein
the first polypeptide consists of amino acid sequence SEQ ID NO:290.
10. The pharmaceutical composition of claim 5 , wherein the composition is suitable for intravenous administration.
11. The pharmaceutical composition of claim 5 , wherein the composition is suitable for subcutaneous administration.
12. The pharmaceutical composition of claim 5 , wherein the composition is suitable for intraperitoneal administration.
13. The pharmaceutical composition of claim 5 , wherein the composition is suitable for intratumoral administration.