Conjugated C1 Esterase Inhibitor and Uses Thereof
The present invention provides, among other things, a conjugated C1-INH for improved treatment of complement-mediated disorders, including hereditary angioedema (HAE). In some embodiments, a conjugated C1-INH provided by the present invention is a PEGylated C1-INH. In some embodiments, a conjugated C1-INH provided by the present invention is a polysialic acid (PSA) conjugated C1-INH.
1 . A composition comprising a conjugated C1 esterase inhibitor (C1-INH) comprising:
a C1-INH protein comprising at least one glycan residue; and
at least one polyethylene glycol (PEG) moiety,
wherein the at least one polyethylene glycol (PEG) moiety is covalently linked to the at least one glycan residue.
2 . A composition comprising a conjugated C1 esterase inhibitor (C1-INH) comprising:
a C1-INH protein comprising at least one polyethylene glycol (PEG) moiety; and
wherein the at least one PEG moiety is covalently linked to the C1-INH protein via an oxime linkage.
3 - 6 . (canceled)
7 . The composition of claim 1 , wherein the C1-INH protein comprises a C1-INH domain having an amino acid sequence at least about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% identical to SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:37, or SEQ ID NO:38.
8 . The composition of claim 1 , wherein the C1-INH protein is a fusion protein.
9 - 22 . (canceled)
23 . The composition of claim 1 , wherein the conjugated C1-INH has a PEG/C1-INH ratio of between about 1 to about 25, between about 1 to about 20, between about 1 to about 15, between about 1 to about 10, or between about 1 to about 5.
24 - 27 . (canceled)
28 . The composition of claim 1 , wherein the conjugated C1-INH has a specific activity in the range of 50%-150% of the specific activity of plasma derived human C-INH.
29 . A method of producing a conjugated C1 esterase inhibitor (C1-INH), said method comprising steps of:
providing a C1-INH protein comprising at least one glycan residue and/or at least one amine group; and
providing a PEG moiety under conditions that permit the PEG moiety reacts with the at least one glycan residue and/or the at least one amine group to form a linkage, thereby producing the conjugated C1-INH.
30 . The method of claim 29 , wherein the PEG moiety comprises PEG-CH 2 —O—NH 2 .
31 - 48 . (canceled)
49 . Use of a composition comprising a conjugated C1-esterase inhibitor of claim 1 , in the manufacture of a medicament for treating a complement mediated disorder.
50 . (canceled)
51 . A composition comprising a conjugated C1 esterase inhibitor (C1-INH) comprising:
a C1-INH protein comprising at least one glycan residue;
at least one polysialic acid (PSA) moiety,
wherein the at least one polysialic acid (PSA) moiety is covalently linked to the at least one glycan residue.
52 . A composition comprising a conjugated C1 esterase inhibitor (C1-INH) comprising
a C1-INH protein comprising at least one glycan residue; and
at least one polysialic acid (PSA) moiety,
wherein the at least one polysialic acid (PSA) moiety is covalently linked to the C1-INH protein via an oxime linkage or a hydrazone linkage.
53 - 57 . (canceled)
58 . The composition of claim 51 , wherein the C1-INH protein comprises a C1-INH domain having an amino acid sequence at least about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% identical to SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:37, or SEQ ID NO:38.
59 - 73 . (canceled)
74 . The composition of claim 51 , wherein the conjugated C1-INH has a PSA/C1-INH ratio of between about 1 to about 25, between about 1 to about 20, between about 1 to about 15, between about 1 to about 10, or between about 1 to about 5.
75 . The composition of claim 51 , wherein the conjugated C1-INH has a half-life comparable or greater that than a plasma derived human C1-INH.
76 - 78 . (canceled)
79 . The composition of claim 51 , wherein the conjugated C1-INH has a specific activity in the range of 50%-150% of the specific activity of plasma derived human C-INH.
80 . A method of producing a conjugated C1 esterase inhibitor (C1-INH), said method comprising steps of:
providing a C1-INH protein comprising at least one glycan residue and/or at least one amine group; and
providing a polysialic acid (PSA) moiety under conditions that permit the PSA moiety to react with the at least one glycan residue and/or the at least one amine group to form a linkage, thereby producing the conjugated C1-INH.
81 - 85 . (canceled)
86 . The method of claim 80 , wherein the molar ratio of PSA to C1-INH is between about 25:1 and 100:1.
87 - 89 . (canceled)
90 . A pharmaceutical composition comprising a conjugated C1 esterase inhibitor (C1-INH) of claim 51 , and a pharmaceutically acceptable carrier.
91 - 92 . (canceled)
93 . A kit comprising a pharmaceutical composition of claim 90 , and a syringe.
94 - 95 . (canceled)
96 . A method of treating a complement-mediated disorder comprising administering to a subject in need of treatment a pharmaceutical composition claim 90 .
97 - 99 . (canceled)