Methods of treating myointimal proliferation
The present invention provides a method of treating myointimal proliferation by administering a recombinant human soluble ectonucleotide pyrophosphatase phosphodiesterase (hsNPP1), active fragment or fusion protein thereof.
1. A method for assessing the effect of ectonucleotide pyrophosphatase pyrophosphorylase 1 (NPP1) treatment on intimal hyperplasia in a tip-toe-walking (ttw) mouse model of carotid artery ligation comprising:
subcutaneously administering a control or NPP1 polypeptide to ttw mice once every other day following carotid ligation;
harvesting carotid arteries from the control and NPP1 treated ttw mice post-administration of the control or NPP1; and
histologically analyzing intimal hyperplasia of the harvested carotid arteries from the NPP1 treated ttw mice compared to the control treated ttw mice, thereby assessing the effect of NPP1 treatment on intimal hyperplasia.
2. The method of claim 1 , wherein the NPP1 polypeptide is a recombinant human NPP1 polypeptide or a recombinant NPP1 fusion protein comprising an Fc region of an immunoglobulin.
3. The method of claim 1 , wherein the intimal hyperplasia results in narrowing of the lumen of a vessel.
4. The method of claim 1 , wherein the NPP1 polypeptide has been administered prior to carotid ligation.
5. A method for determining the effect of ectonucleotide pyrophosphatase pyrophosphorylase 1 (NPP1) treatment on intimal hyperplasia in response to a mechanical injury to a vasculature in an animal model of generalized arterial calcification of infancy (GACI), the method comprising:
measuring intimal hyperplasia in the vasculature of the animal following treatment with an NPP1 polypeptide, wherein the animal has been administered the NPP1 polypeptide prior to mechanical injury, following mechanical injury, or both prior to and following a mechanical injury to the vasculature of the animal, and
comparing the intimal hyperplasia in the animal treated with the NPP1 polypeptide with a control animal that has been treated with vehicle and not with the NPP1 polypeptide,
thereby determining the effect of treatment with the NPP1 polypeptide on intimal hyperplasia in response to the mechanical injury of the vasculature.
6. The method of claim 5 , wherein the animal model is a mouse.
7. The method of claim 6 , wherein the animal model of GACI is a tip-toe-walking (ttw) mouse.
8. The method of claim 6 , wherein the mechanical injury is carotid artery ligation.
9. The method of claim 6 , wherein the NPP1 polypeptide has been administered prior to mechanical injury or prior to and following mechanical injury.
10. The method of claim 6 , wherein the NPP1 polypeptide has been administered subcutaneously.
11. The method of claim 6 , wherein the NPP1 polypeptide is a recombinant human NPP1 polypeptide or a recombinant NPP1 fusion protein comprising an Fc region of an immunoglobulin.
12. The method of claim 6 , wherein the intimal hyperplasia results in narrowing of the lumen of a vessel.
13. The method of claim 5 , wherein the animal model of GACI is a tip-toe-walking (ttw) mouse.
14. The method of claim 5 , wherein the mechanical injury is carotid artery ligation.
15. The method of claim 5 , wherein the NPP1 polypeptide has been administered prior to mechanical injury, and optionally after or prior to and following mechanical injury.
16. The method of claim 5 , wherein the NPP1 polypeptide has been administered subcutaneously.
17. The method of claim 5 , wherein the NPP1 polypeptide is a recombinant human NPP1 polypeptide or a recombinant NPP1 fusion protein comprising an Fc region of an immunoglobulin.
18. The method of claim 5 , wherein the intimal hyperplasia results in narrowing of the lumen of a vessel.