SYNTHETIC HYPERGLYCOSYLATED, PROTEASE-RESISTANT POLYPEPTIDE VARIANTS, ORAL FORMULATIONS AND METHODS OF USING THE SAME
First Claim
1. A hyperglycosylated Type I interferon variant of a parent Type I interferon, wherein the hyperglycosylated Type I interferon is the parent Type I interferon that has been modified to include at least two additional glycosylation sites, wherein at least one of the additional glycosylation sites is introduced by an amino acid substitution at a position selected from amino acid position 99, 105 and 134, wherein the positions of the amino acid substitutions are with reference to sequence alignment numbering set forth in FIG. 24.
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Accused Products
Abstract
The present invention provides synthetic Type I interferon receptor polypeptide agonists comprising consensus or hybrid Type I interferon receptor polypeptide agonists, containing one or more native or non-native glycosylation sites. The present invention further provides oral formulations of protease-resistant or protease-resistant, hyperglycosylated polypeptide variants, which polypeptide variants lack at least one protease cleavage site found in a parent polypeptide, and thus exhibit increased protease resistance compared to the parent polypeptide, which polypeptide variants further include (1) a carbohydrate moiety covalently linked to at least one non-native glycosylation site not found in the parent protein therapeutic or (2) a carbohydrate moiety covalently linked to at least one native glycosylation site found but not glycosylated in the parent protein therapeutic. The present invention further provides compositions, including oral pharmaceutical compositions, comprising the synthetic Type I interferon receptor polypeptide agonist, the hyperglycosylated polypeptide variant, the protease-resistant polypeptide variant, or the hyperglycosylated, protease-resistant polypeptide variant. The present invention further provides containers, devices, and kits comprising the synthetic Type I interferon receptor polypeptide agonist, the hyperglycosylated polypeptide variant, the protease-resistant polypeptide variant, or the hyperglycosylated, protease-resistant polypeptide variant. The present invention further provides therapeutic methods involving administering an effective amount of an oral pharmaceutical composition comprising a synthetic Type I interferon receptor polypeptide agonist, a hyperglycosylated polypeptide variant, a protease-resistant polypeptide variant, or a hyperglycosylated, protease-resistant polypeptide variant to an individual in need thereof.
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Citations
20 Claims
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1. A hyperglycosylated Type I interferon variant of a parent Type I interferon, wherein the hyperglycosylated Type I interferon is the parent Type I interferon that has been modified to include at least two additional glycosylation sites, wherein at least one of the additional glycosylation sites is introduced by an amino acid substitution at a position selected from amino acid position 99, 105 and 134, wherein the positions of the amino acid substitutions are with reference to sequence alignment numbering set forth in
FIG. 24 .
Specification