Compositions and methods for treating pathological calcification and ossification
The present invention includes compositions and methods for treating disease and disorders associated with pathological calcification or pathological ossification by modulating the level or activity of NPP1 or a mutant thereof, or a mutant NPP4 modified to exhibit ATP hydrolase activity similar to the hydrolase activity of NPP1.
1 . A method of treating or ameliorating a disease or disorder associated with or caused by an improper serum pyrophosphate (PPi) and phosphate (Pi) balance (PPi/Pi homeostasis) in a subject,
the method comprising administering to the subject a therapeutically effective amount of a composition comprising a soluble ecto-nucleotide pyrophosphatase/phosphodiesterase-1 (ENPP1) polypeptide or a biologically active fragment, derivative, mutant, or mutant fragment thereof,
wherein the soluble ENPP1 polypeptide lacks a targeting domain consisting of 4-20 sequential aspartic acid residues,
wherein the administering increases serum PPi levels in the subject relative to the serum PPi levels in the subject before the administration, and thereby treating or ameliorating the disease or disorder in the subject.
2 . The method of claim 1 , wherein the soluble ENPP1 polypeptide comprises a somatomedin B domain, an ENPP1 catalytic domain, and an ENPP1 nuclease domain.
3 . The method of claim 1 , wherein the soluble ENPP1 polypeptide comprises residues 96-925 of human ENPP1 (SEQ ID NO: 1).
4 . The method of claim 1 , wherein the soluble ENPP1 polypeptide is a secreted product of a precursor polypeptide expressed in a mammalian cell, wherein the precursor polypeptide comprises an ecto-nucleotide pyrophosphatase/phosphodiesterase-2 (ENPP2) signal sequence and an ENPP1 polypeptide, wherein the precursor polypeptide undergoes proteolytic processing to the soluble ENPP1 polypeptide.
5 . The method of claim 1 , wherein the soluble ENPP1 polypeptide is a secreted product of a precursor polypeptide expressed in a mammalian cell, wherein the precursor polypeptide comprises residues 12-30 of ENPP2 (SEQ ID NO: 2), which is fused to the N-terminus of a polypeptide comprising a somatomedin B domain, an ENPP1 catalytic domain, and an ENPP1 nuclease domain, wherein the precursor polypeptide undergoes proteolytic processing to the soluble ENPP1 polypeptide.
6 . The method of claim 1 , wherein the soluble ENPP1 polypeptide is a secreted product of a precursor polypeptide expressed in a mammalian cell, wherein the precursor polypeptide lacks residues 77-98 of the ENPP1 transmembrane domain and comprises a signal sequence, wherein the precursor polypeptide undergoes proteolytic processing to the soluble ENPP1 polypeptide.
7 . The method of claim 1 , wherein the ENPP1 polypeptide is a secreted product of a precursor polypeptide expressed in a mammalian cell, wherein the precursor polypeptide comprises residues 1-76 of ENPP1 (SEQ ID NO: 1), residues 12-30 of ENPP2 (SEQ ID NO: 2), and residues 96-925 of ENPP1 (SEQ ID NO: 1), wherein the precursor polypeptide undergoes proteolytic processing to the soluble ENPP1 polypeptide.
8 . The method of claim 1 , wherein the soluble ENPP1 polypeptide is a fusion protein comprising an IgG Fc domain.
9 . The method of claim 1 , wherein the soluble ENPP1 polypeptide has ATP hydrolytic activity.
10 . The method of claim 1 , wherein the soluble ENPP1 polypeptide is administered acutely or chronically to the subject.
11 . The method of claim 6 , wherein the soluble ENPP1 polypeptide is administered locally, regionally, parenterally, or systemically to the subject.
12 . The method of claim 1 , wherein the subject is human.
13 . The method of claim 1 , wherein the disease or disorder is at least one selected from the group consisting of idiopathic infantile arterial calcification (IIAC), ossification of the posterior longitudinal ligament (OPLL), hypophosphatemic rickets, osteoarthritis, and calcification of atherosclerotic plaques.
14 . The method of claim 1 , wherein increase in serum PPi levels reduces pathological calcification of soft tissue in the subject.
15 . The method of claim 14 , wherein the soft tissue comprises one or more of atherosclerotic plaques, muscular arteries, joints of the hands, joints of the feet, spine, articular cartilage, connective tissue, and vertebral disk cartilage.
16 . The method of claim 1 , wherein the subject has a loss of function mutation in the gene encoding ecto-nucleotide pyrophosphatase/phosphodiesterase-1 (ENPP1).