Col 11A1 AND NOVEL FRAGMENT THEREOF FOR REGULATION OF BONE MINERALIZATION

Patent metadata

Field	Value
Publication number	US-2016331814-A1
Application number	US-201615131544-A
Country	US
Kind code	A1
Filing date	Apr 18, 2016
Priority date	Apr 24, 2015
Publication date	Nov 17, 2016
Grant date	—

Abstract

The present invention relates to the discovery that the collagen 11a1 (Col 11A1) protein, and/or fragments thereof, may be used to modulate bone mineralization. In some embodiments, bone mineralization is promoted by the addition of Col 11A1 or a fragment thereof, by pharmaceutical compositions that increase the presence of Col 11A1, and in some embodiments, bone mineralization may desired to be inhibited by pharmaceutical compositions that interfere, impede, or inhibit Col 11A1. The invention includes compositions including a Col 11A1 polypeptide, or fragment and compositions including a nucleic acid that encodes a Col 11A1 polypeptide or fragment. The invention also provides methods and kits for using such polypeptides and nucleic acids to treat bone mineralization disorders, and promote bone growth and fracture healing.

First claim

What is claimed is:

1 . A method of modulating bone matrix mineralization in a subject, said method comprising administering to said subject a therapeutically effective amount of a pharmaceutical composition comprising:
(a) a Col 11A1 protein or inhibitor thereof; and (b) a pharmaceutically acceptable carrier.

2 . The method of claim 1 , wherein (a) said Col 11A1 protein is a Col 11A1 fragment.

3 . The method of claim 1 wherein said Col 11A1 protein is one or more of the following:
(a) the amino acid sequence of SEQ ID NOS: 1, 2, or 3;
(b) the amino acid sequence at least 85% sequence identity to SEQ ID NO: 1, 2, or 3;
(c) a conservatively modified variant of SEQ ID NOS: 1, 2, or 3;
(d) a fragment of 1,2, or 3 wherein said fragment modulation bone mineralization.

4 . The method of claim 2 , wherein said fragment is SEQ ID NO:1.

5 . The method of claim 1 , wherein said carrier is saline.

6 . The method of claim 1 , wherein (a) said polypeptide is pegylated, (b) said polypeptide is glycosylated, (c) said pharmaceutical composition comprises a dimer of said polypeptide, (d) said pharmaceutically acceptable excipient comprises saline, or (e) said pharmaceutical composition is lyophilized.

7 . The method of claim 1 , wherein said pharmaceutical composition is administered subcutaneously, intravenously, orally, nasally, intramuscularly, sublingually, intrathecally, or intradermally.

8 . The method of claim 1 wherein said subject in need of bone mineralization is a subject suffering from a bone fracture.

9 . The method of claim 1 wherein said subject is suffering from a bone mineralization disease.

10 . The method of claim 9 , wherein said bone mineralization disorder is hypophosphatasia, optionally wherein said matrix mineralization disorder is infantile hypophosphatasia (HPP), childhood HPP, perinatal HPP, adult HPP, or odontohypophosphatasia.

11 . The method of claim 8 wherein said subject is suffering from osteoporosis.

12 . The method of claim 1 , wherein said subject is human.

13 . A pharmaceutical composition comprising:
(a) a Col 11A1 polypeptide; and (b) a pharmaceutically acceptable carrier.

14 . A method of modulating bone mineralization in a subject, said method comprising administering to said subject a therapeutically effective amount of a pharmaceutical composition comprising:
(a) an isolated nucleic acid molecule encoding a Col 11A1 polypeptide; and (b) a pharmaceutically acceptable carrier.

15 . The method of claim 14 wherein said pharmaceutical composition is an expression vector.

16 . The method of claim 15 wherein said expression vector is a lentiviral vector.

17 . An isolated recombinant host cell transformed or transfected with a lentiviral recombinant expression vector comprising the isolated nucleic acid molecule of claim 14 .

18 . The method of claim 14 wherein said expression vector is an inhibition construct.

19 . The method of claim 18 wherein said inhibition construct is an antisense oligonucleotide.

20 . The method of claim 19 wherein said antisense oligonucleotide is a morpholino oligonucleotide.

21 . A pharmaceutical composition comprising:
(a) an isolated nucleic acid molecule encoding a Col 11A1 polypeptide; and (b) a pharmaceutically acceptable carrier.

22 . The pharmaceutical composition of claim 21 wherein said nucleic acid is an expression vector.

23 . The pharmaceutical composting of claim 22 wherein said expression vector is a lentiviral vector.

24 . The pharmaceutical composition of claim 21 wherein said expression vector is an inhibition construct.

25 . The pharmaceutical composition of claim 24 wherein said inhibition construct is an antisense oligonucleotide.

26 . The pharmaceutical composition of claim 25 wherein said antisense oligonucleotide is a morpholino oligonucleotide.

27 . An Col 11a1 fragment wherein the Col 11A1 fragment comprises SEQ ID NO:1 and is less that the full length Col 11A1 sequence of SEQ IN NO: 1 or 2.

28 . A nucleic acid sequence encoding the Col 11A1 fragment of claim 27 .

29 . The isolated nucleic acid molecule of claim 28 operably linked to a promoter.

30 . An expression vector comprising the isolated nucleic acid molecule of claim 28 .

31 . The expression vector of claim 30 , wherein the expression vector comprises a promoter, wherein the promoter is a cytomegalovirus promoter.

32 . The expression vector of claim 31 , further encoding a selectable marker.

33 . The expression vector of claim 31 , wherein the expression vector comprises a mammalian expression vector.

34 . The expression vector of claim 30 , wherein the mammalian expression vector comprises a viral expression vector.

35 . A viral particle comprising the expression vector of claim 33 .

Assignees

• Univ Boise State

Inventors

• Oxford Julia Thom

Classifications

• C12N2740/16043

  viral genome or elements thereof as genetic vector · CPC title

• C07K2319/40

  containing a tag for immunodetection, or an epitope for immunisation · CPC title

• C07K14/78

  Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin or cold insoluble globulin [CIG] · CPC title

• A61K38/39 Primary

  Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin, cold insoluble globulin [CIG] · CPC title

• A61K48/005

  characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered · CPC title