Compositions and methods for the treatment of viral infections
Compositions and methods for the treatment of viral infections include conjugates containing inhibitors of viral neuraminidase (e.g., zanamivir, peramivir, or analogs thereof) linked to an Fc monomer, an Fc domain, and Fc-binding peptide, an albumin protein, or albumin-binding peptide. In particular, conjugates can be used in the treatment of viral infections (e.g., influenza viral infections).
1. A conjugate described by formula (D-I):
wherein each of A1 and A2 is zanamivir;
E comprises an Fc domain monomer comprising an amino acid sequence selected from any one of SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 67, and SEQ ID NO: 68, wherein each Fc domain optionally lacks C-terminal Lys447;
L is a linker covalently attached to each of A1, A2, and E, wherein L is covalently attached to each of A1 and A2 independently at position C7 or position C9 of zanamivir;
n is 1 or 2; and
T is the number of A 1 -L-A 2 moieties conjugated to each E and each T is, independently, an integer from 1 to 20;
or a pharmaceutically acceptable salt thereof.
2. The conjugate of claim 1 , wherein each L is covalently attached to the nitrogen atom of a surface exposed lysine of E.
3. The conjugate of claim 1 , wherein each L is covalently attached to the sulfur atom of a surface exposed cysteine of E.
4. The conjugate of claim 1 , wherein n is 2, and the two Es dimerize with each other to form an Fc domain.
5. The conjugate of claim 1 , wherein T is an integer from 1 to 10.
6. A population of conjugates of claim 1 , wherein the average value of T is 1 to 5.
7. The conjugate of claim 1 , wherein each E comprises an amino acid sequence of SEQ ID NO: 63.
8. The conjugate of claim 1 , wherein each E comprises an amino acid sequence of SEQ ID NO: 64.
9. The conjugate of claim 1 , wherein each E comprises an amino acid sequence of SEQ ID NO: 67.
10. The conjugate of claim 1 , wherein each E comprises an amino acid sequence of SEQ ID NO: 68.