TNF receptor Fc fusion proteins and in vivo methods of use
The embodiments of the invention relate to compositions, methods, and kits comprising a fusion protein. The fusion proteins of the embodiments include monomer polypeptides which in one embodiment have at least a binding domain, an optional hinge region, a collagen-like domain and the Fc domain of a human IgG.
1. A fusion protein comprising three or six monomer polypeptides, wherein each monomer polypeptide independently comprises:
(a) a single domain antibody, or an extracellular domain of a TNF receptor in a TNF receptor family,
(b) a collagen-like domain comprising at least 8 G-P-X1 blocks, a trimerizing motif, and wherein X1 is P or O,
(c) optionally, a hinge region of IgG or a glycine linker, and
(d) an Fc domain comprising the CH2 and CH3 regions of human IgG
wherein the trimerizing motif comprises SEQ ID NO: 34, or a variation thereof which comprises one or more of the following structures: SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, and SEQ ID NO: 45.
2. The fusion protein of claim 1 , wherein the extracellular domain of a TNF receptor family is the sequence of the extracellular domain of at least one TNF receptor selected from the group consisting of TNFαRII (p55), TNFR type II (p75), Fas (CD95), CD40, CD27, CD30, 4-1BB (CDw137), OX40 (CD134), LTBR, NGFR (CD271), DcR3, TRAILR-1 (CD261), TRAILR-2 (CD262), TRAILR-3 (CD263), TRAILR-4 (CD264), RANK (CD265), OPG (TR1), FN14 (CD266), TACI (CD267), BAFFR (CD268), HVEM (CD270), BCM (CD269), GITR (CD357), TAJ-alpha (TROY), DR6 (CD358), and DR3 (TRAMP).
3. The fusion protein of claim 1 , wherein the trimerizing motif is located in between two G-P-X1 blocks.
4. The fusion protein of claim 1 , wherein in each monomer polypeptide, the collagen-like domain amino acid sequence is selected from group consisting of:
SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 35, SEQ ID NO: 22, and SEQ ID NO: 25.
5. The fusion protein of claim 1 , wherein the Fc domain is C-terminal to the collagen-like domain.
6. The fusion protein of claim 2 , wherein the extracellular domain of a TNF receptor in a TNF receptor family is the extracellular domain of TNFR type II (p75).
7. The fusion protein of claim 1 , wherein the trimerizing motif comprises SEQ ID NO: 40.
8. The fusion protein of claim 4 , wherein in each monomer polypeptide, the collagen-like domain amino acid sequence is SEQ ID NO: 22.
9. A kit comprising the fusion protein of claim 1 .
10. A fusion protein comprising three or six monomer polypeptides:
where each monomer polypeptide independently comprises an amino acid sequence having at least 90, 92, 95, 97, 99, or 100% sequence identity to at least one of the amino acid sequences selected from the group consisting of SEQ ID NOs: 1, 3, 5, 7, 9, 11, and 13, and wherein the polypeptides bind to and inhibit TNFα.
11. A fusion protein comprising three or six monomer polypeptides:
where each monomer polypeptide independently comprises an amino acid sequence having at least 90, 92, 95, 97, 99, or 100% sequence identity to SEQ ID NO: 9, and wherein the polypeptides bind to and inhibit TNFα.
12. A nucleic acid encoding a monomer polypeptide of the fusion protein of claim 1 .
13. An expression vector that expresses the fusion protein of claim 1 .
14. An isolated host cell comprising the expression vector of claim 13 .
15. A method of lowering the level of TNFα signaling in vivo comprising administering to a patient in need thereof an effective amount of a protein comprising:
a fusion protein having three or six monomer polypeptides, wherein each polypeptide comprises:
(a) a single domain antibody or an extracellular domain of a TNF receptor in a TNF receptor family,
(b) a collagen-like domain comprising at least 8 G-P-X1 blocks, a trimerizing motif, and wherein X1 is P or O,
(c) optionally, a hinge region of IgG or a glycine linker, and
(d) an Fc domain comprising the CH2 and CH3 regions of human IgG
wherein the trimerizing motif comprises SEQ ID NO: 34, or a variation thereof which comprises one or more of the following structures: SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, and SEQ ID NO: 45.
16. A method of treating one or more of rheumatoid arthritis, inflammatory bowel disease, psoriatic arthritis, vasculitis, ankylosing spondylitis, and juvenile chronic arthritis comprising administering to a patient in need thereof an effective amount of a composition comprising:
a fusion protein comprising three or six monomer polypeptides, wherein each polypeptide comprises:
(a) an extracellular domain of a TNF receptor in a TNF receptor family,
(b) a collagen-like domain comprising at least 8 G-P-X1 blocks, a trimerizing motif, wherein X1 is P or O, wherein the trimerizing motif comprises SEQ ID NO: 34, or a variation thereof which comprises one or more of the following structures: SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, and SEQ ID NO: 45,
(c) optionally a hinge region of IgG or a glycine linker, and
(d) an Fc domain comprising the CH2 and CH3 regions of human IgG,
in a pharmaceutically acceptable carrier.
17. The method of claim 16 , comprising administering 0.01-100.0 mg/kg of the composition.