Therapeutic modulation of chemokines using a helminth parasite chemokine-binding protein

• US 20030124124A1
• Filed: 11/14/2002
• Published: 07/03/2003
• Est. Priority Date: 06/27/2001
• Status: Abandoned Application

• Current Assignee: Cambridge University (Government of United Kingdom)
• Original Assignee: Cambridge University (Government of United Kingdom)
• Inventors: Smith, Philip, Fallon, Padraic, Alcami, Antonio
• Application Number:
  US10/293,950
• Publication Number:
  US 20030124124A1
• Time in Patent Office: Days
• US Class Current: 424/145.1
• CPC Class Codes: C07K 14/43559 from trematodes
• CPC Class Codes: C12N 2799/026 where the vector is derived from a baculovirus

Abstract

ES-2 polypeptide encoding nucleic acid has been cloned from Schistosoma mansoni and shown to bind and inhibit chemokine function, including CC chemokines such as MIP-1α and/or RANTES, CXC chemokines such as IL-8, C chemokines and CX₃C chemokines, both in vivo and in vitro. The polypeptide is useful in therapy of inflammatory disorders and other diseases, and in assaying for substances with ability to potentiate or inhibit its anti-chemokine function, which substances have additional therapeutic potential.

Claims

1. A method of producing a polypeptide which has chemokine-binding activity, the method comprising:

(a) causing expression from nucleic acid which encodes a polypeptide which is a chemokine-binding molecule in a suitable expression system to produce the polypeptide,

wherein the polypeptide is a chemokine-binding molecule which comprises the amino acid sequence of SEQ ID NO. 2 or consists of a portion of the amino acid sequence of SEQ ID NO. 2 that is chemokine-binding, or which has an amino acid sequence which differs from the amino acid sequence of SEQ ID NO. 2 but has at least 35% and preferably at least 70% identity with the amino acid sequence of SEQ ID NO. 2 and is chemokine-binding; and

(b) testing the polypeptide for chemokine-binding activity or ability to inhibit chemokine activity.

2. A method according to claim 1 wherein the polypeptide has at least 90% identity with the amino acid sequence of SEQ ID NO. 2.

3. A method according to claim 1 wherein said polypeptide comprises the amino acid sequence of SEQ ID NO. 2.

4. A method according to claim 3 wherein said nucleic acid comprises the nucleotide sequence of SEQ ID NO. 1.

5. A method according to claim 1 comprising isolating the polypeptide.

6. A method according to claim 5 comprising testing the polypeptide for ability to inhibit chemokine activity.

7. A method according to claim 1 wherein the polypeptide inhibits chemokine activity.

8. A method according to claim 1 further comprising formulating the polypeptide into a composition comprising at least one additional component.

10. A method according to claim 1 further comprising bringing the polypeptide into contact with a chemokine to inhibit activity of the chemokine.

11. A method according to claim 10 wherein the chemokine is contacted with the polypeptide in vitro.

12. A method according to claim 10 comprising administering the polypeptide to an individual.

13. A method according to claim 12 wherein the individual has a disease or disorder involving activity of a chemokine, which activity is inhibited by the polypeptide.

14. A method according to claim 1 further comprising employing the polypeptide in a diagnostic product.

15. A nucleic acid construct suitable for use in a method of producing a polypeptide as defined in claim 1, the construct comprising a nucleotide sequence which encodes the polypeptide and which is operably linked to regulatory sequences for expression of the encoded polypeptide.

16. A nucleic acid construct according to claim 15 wherein the encoded polypeptide comprises the amino acid sequence of SEQ ID NO. 2.

17. A nucleic acid construct according to claim 16 wherein said nucleic acid comprises the nucleotide sequence of SEQ ID NO. 1.

18. A nucleic acid construct according to claim 15 wherein the polypeptide which is a chemokine-binding molecule consists of a portion of the amino acid sequence of SEQ ID NO. 2 that is chemokine-binding.

19. A nucleic acid construct according to claim 15 wherein the polypeptide which is a chemokine-binding molecule has an amino acid sequence which differs from the amino acid sequence of SEQ ID NO. 2 but has at least 35% and preferably at least 70% identity with the amino acid sequence of SEQ ID NO. 2.

20. A nucleic acid construct according to claim 19 wherein the polypeptide has at least 90% identity with the amino acid sequence of SEQ ID NO. 2.

21. A host cell transformed with a nucleic acid construct according to claim 15.

22. Use of a nucleic acid construct according to claim 15 in a method for producing a polypeptide which is a chemokine-binding molecule.

23. A isolated polypeptide produced by a method according to claim 1.

24. A method of treatment of a disease or disorder comprising administration of a polypeptide according to claim 23 to an individual, wherein the individual has a disease or disorder involving activity of a chemokine, which activity is inhibited by the polypeptide.

25. Use of a polypeptide according to claim 23 in the manufacture of a medicament for treatment of a disease or disorder involving activity of a chemokine, which activity is inhibited by the polypeptide.

26. Use of a polypeptide according to claim 23 in screening for or obtaining a substance which binds the polypeptide and optionally affects chemokine-binding ability of the polypeptide.

27. An assay method for a substance which binds a polypeptide, which polypeptide is a chemokine-binding molecule which comprises the amino acid sequence of SEQ ID NO. 2 or consists of a portion of the amino acid sequence of SEQ ID NO. 2 that is chemokine-binding, or which has an amino acid sequence which differs from the amino acid sequence of SEQ ID NO. 2 but has at least 35% and preferably at least 70% identity with the amino acid sequence of SEQ ID NO. 2 and is chemokine-binding, the method comprising:

(a) bringing into contact the polypeptide and a putative binding molecule or other test substance; and

(b) determining binding between the polypeptide and the test substance.

28. An assay method for a substance that affects chemokine-binding of a polypeptide, wherein the polypeptide is a chemokine-binding molecule which comprises the amino acid sequence of SEQ ID NO. 2 or consists of a portion of the amino acid sequence of SEQ ID NO. 2 that is chemokine-binding, or which has an amino acid sequence which differs from the amino acid sequence of SEQ ID NO. 2 but has at least 35% and preferably at least 70% identity with the amino acid sequence of SEQ ID NO. 2 and is chemokine-binding, the method comprising:

(a) bringing into contact a substance comprising the polypeptide, a second substance comprising a chemokine polypeptide which is able to bind the polypeptide which is a chemokine-binding molecule; and

a test compound, under conditions in which in the absence of the test compound being an inhibitor, the two said substances interact;

(b) determining interaction between said substance.

29. An assay method for a substance that affects ability of a polypeptide to inhibit chemokine activity, wherein the polypeptide is a chemokine-binding molecule which comprises the amino acid sequence of SEQ ID NO. 2 or consists of a portion of the amino acid sequence of SEQ ID NO. 2 that is chemokine-binding, or which has an amino acid sequence which differs from the amino acid sequence of SEQ ID NO. 2 but has at least 35% and preferably at least 70% identity with the amino acid sequence of SEQ ID NO. 2 and is chemokine-binding, the method comprising:

(a) incubating the polypeptide and a test compound in the presence of a chemokine such as a CC chemokine such as MIP-1α and

/or RANTES, and/or a CXC chemokine such as IL-8, under conditions in which chemokine activity is inhibited by the polypeptide; and

(b) determining chemokine activity.