Methods and compositions for treating secondary tissue damage and other inflammatory conditions and disorders

• US 20030215421A1
• Filed: 02/24/2003
• Published: 11/20/2003
• Est. Priority Date: 07/21/1999
• Status: Abandoned Application

• Current Assignee: Osprey Pharmaceuticals USA, Inc. (Osprey Pharmaceuticals Limited)
• Original Assignee: Osprey Pharmaceuticals USA, Inc. (Osprey Pharmaceuticals Limited)
• Inventors: Coggins, Philip J., McDonald, John R.
• Application Number:
  US10/375,209
• Publication Number:
  US 20030215421A1
• Time in Patent Office: Days
• US Class Current: 424/85.1
• CPC Class Codes: A61K 2039/505 comprising antibodies
• CPC Class Codes: A61K 38/00 Medicinal preparations containing peptides peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00
• CPC Class Codes: A61K 47/6415 Toxins or lectins, e.g. clostridial toxins or Pseudomonas exotoxins
• CPC Class Codes: A61K 47/642 the peptide or protein in the drug conjugate being a cytokine, e.g. IL2, chemokine, growth factors or interferons being the inactive part of the conjugate
• CPC Class Codes: A61K 47/6425 the peptide or protein in the drug conjugate being a receptor, e.g. CD4, a cell surface antigen, i.e. not a peptide ligand targeting the antigen, or a cell surface determinant, i.e. a part of the surface of a cell
• CPC Class Codes: A61P 31/12 Antivirals
• CPC Class Codes: C07H 21/04 with deoxyribosyl as saccharide radical
• CPC Class Codes: C07K 14/415 from plants
• CPC Class Codes: C07K 14/521 Chemokines
• CPC Class Codes: C07K 16/2866 against receptors for cytokines, lymphokines, interferons
• CPC Class Codes: C07K 17/00 Carrier-bound or immobilised peptides carrier-bound or immobilised enzymes C12N11/00; Preparation thereof
• CPC Class Codes: C07K 2317/77 Internalization into the cell
• CPC Class Codes: C07K 2319/00 Fusion polypeptide
• CPC Class Codes: C07K 2319/33 fusions for targeting to specific cell types, e.g. tissue specific targeting, targeting of a bacterial subspecies
• CPC Class Codes: C07K 2319/55 containing a fusion with a toxin, e.g. diphteria toxin

Abstract

Nucleic acid moleucles that encode conjugates containing as a ligand a chemokine receptor targeting agents, such as chemokines, and a targeted agent, such as a toxin are provided. These conjugates are used to treat inflammatory responses associated with activation, proliferation and migration of immune effector cells, including leukocyte cell types, neutrophils, macrophages, and eosinophils.

Claims

1. A conjugate, comprising a targeted agent and a chemokine receptor targeting agent, or a portion thereof, wherein the conjugate binds to a receptor resulting in internalization of the linked targeted agent in cells bearing the receptor, wherein the receptor is selected from the group consisting of CXCR4, CCR2b, CCR3, CCR5, CCR6, CCR8 and CX3CR1.

2. A conjugate of claim 1, comprising the following components:

(chemokine receptor targeting agent)_n, (L)_q and (targeted agent)_m, wherein;

L is a linker for linking the chemokine receptor targeting agent to a targeted agent;

the chemokine receptor targeting agent is any moiety that selectively binds a receptor selected from the group consisting of CXCR4, CCR2b, CCR3, CCR5, CCR6, CCR8 and CX3CR1;

m and n, which are selected independently, are at least 1;

q is 0 or more as long as the resulting conjugate binds to the targeted receptor, is internalized and delivers the targeted agent; and

the resulting conjugate binds to a receptor selected from the group consisting of CXCR4, CCR2b, CCR3, CCR5, CCR6, CCR8 and CX3CR1, whereby the targeted agent(s) is internalized in a cell bearing the receptor.

3. The conjugate of claim 2, wherein m and n, which are selected independently, are 1-6.

4. The conjugate of claim 2, wherein q is 1, n is 1 and m is 1.

5. The conjugate of claim 1, wherein the chemokine receptor targeting agent is a chemokine, an antibody that specifically binds to a chemokine receptor or a fragment of the chemokine or antibody, wherein the fragment binds to the receptor and internalizes the targeted agent, and the receptor is selected from the group consisting of CXCR4, CCR2b, CCR3, CCR5, CCR6, CCR8 and CX3CR1.

6. The conjugate of claim 1, wherein the receptor is expressed on CD4+ cells.

7. The conjugate of claim 6, wherein the CD4+ cells are infected with HIV.

8. The conjugate of claim 1, wherein receptor is expressed on mononuclear phagocytes (MNPs).

9. The conjugate of claim 1, wherein that CXCR4 receptor targeting agent is selected from the group consisting of SDF-1α

, SDF-1β

, and SDF-Eotaxin, RANTES and MDC.

10. The conjugate of claim 1, wherein the targeted agent is a toxin, a nucleic acid or a therapeutic protein.

11. The conjugate of claim 10, wherein the cell toxin is a DNA cleaving agent.

12. The conjugate of claim 11, wherein the DNA cleaving agent is selected from among anthraquinone-oligopyrrolcarboxamide, benzimidazole, leinamycin, dynemycin A, enediyne, endiyne quinone imines, 2,2r-bis (2-aminoethyl)-4-4′

-bithiazole, epilliticine-salen.copper conjugates, and functional analogs or derivatives thereof.

13. The conjugate of claim 10, wherein the toxin is an antimetabolite.

14. The conjugate of claim 13, wherein the antimetabolite is selected from among of 5-fluorouracil, methotrexate, melphalan, daunomycin, doxorubicin, nitrogen mustard, mitomycin c, and functional analogs or derivatives thereof.

15. The conjugate of claim 10, wherein the toxin is selected from among bacterial, plant, insect, snake and spider toxins.

16. The conjugate of claim 15, wherein the cell toxin is selected from the group consisting of bacterial, plant, insect, snake and spider toxins.

17. The conjugate of claim 16, wherein the cell toxin is a ribosome inactivating protein (RIP).

18. The conjugate of claim 17, wherein the RIP is a type one RIP or a biologically functional fragment thereof.

19. The conjugate of claim 18, wherein the type one RIP is selected from the group consisting of dianthin 30, dianthin 32, lychnin, saporin-1, saporin-2, saporin-3, saporin-4, saporin-5, saporin-6, saporin-7, saporin-8 and saporin-9, PAP, PAP II, PAP-R, PAP-S, PAP-C, mapalmin, dodecandrin, bryodin-L, bryodin, colicin-1, colicin-2, luffin-A, luffin-B, luffin-S, 19K-PSI, 15K-PSI, 9K-PSI, alpha-kirilowin, beta-kirilowin, gelonin, momordin, momordin-II, momordin-Ic, MAP-30, alpha-momorcharin, beta-momorcharin, trichosanthin, TAP-29, trichokirin, barley RIP, tritin, flax RIP, corn RIP, asparin-1, and asparin-2.

20. The conjugate of claim 19, wherein the RIP is a type two RIP, the catalytic subunit thereof, or a biologically functional subunit or fragment thereof.

21. The conjugate of claim 20, wherein the type two RIP is selected from the group consisting of volkensin, ricin, nigrin-CIP-29, abrin, vircumin, modeccin, ebulitin-α

, ebulitin-β

, ebultin-γ

, and porrectin.

22. The conjugate of claim 21, wherein the toxin is a bacterial toxin selected from among Pseudomonas exotoxin, Diphtheria toxin, shiga toxin, shiga-like toxins, catalytic subunits thereof, and biologically functional fragments thereof.

23. The conjugate of claim 1, wherein the chemokine receptor targeting agent and targeting agent are linked directly via a covalent or ionic linkage.

24. The conjugate of claim 1, wherein the chemokine receptor targeting agent and targeting agent are joined via a linker.

25. The conjugate of claim 24, wherein the linker is a polypeptide or is chemical linker.

28. The conjugate of claim 24, wherein the linker is a peptide or an amino acid

29. The conjugate of claim 28, wherein the peptide comprises between 1 and 60 amino acids.

30. The conjugate of claim 29, wherein the linker is selected from among peptides that reduce stearic hindrance between the targeted agent and chemokine receptor targeting agent, intracellular enzyme substrates, linkers that increase the flexibility of the conjugate, linkers that increase the solubility of the conjugate, linkers that increase the serum stability of the conjugate, photocleavable linkers and acid cleavable linkers.

31. The conjugate of claim 1, wherein the chemokine receptor targeting agent is a monoclonal antibody, or an antigen-specific fragment thereof.

32. A nucleic acid molecule, comprising a sequence of nucleotides encoding a conjugate of any of claims 1-8, 15-25, 28, 29 and 31.

33. A plasmid, comprising the nucleic acid molecule of claim 32.

34. A host cell, comprising the plasmid of claim 33.

35. A method of producing a conjugate, comprising culturing the cell of claim 34 under conditions, whereby a fusion protein comprising the conjugate is expressed, and isolating the fusion protein.

36. A pharmaceutical composition comprising a therapeutically effective concentration or amount of a conjugate any of claims 1-31 in a pharmaceutically acceptable vehicle.

37. A method of treatment of HIV infection, comprising administering a composition of claim 36.

26. The conjugate of 24, wherein the chemical linker is a heterobifunctional cleavable cross-linker.

27. The conjugate of claim 26, wherein the chemical linker is selected from among N-succinimidyl (4-iodoacetyl)-aminobenzoate, sulfosuccinimydil (4-iodoacetyl)-aminobenzoate, 4-succinimidyl-oxycarbonyl-a-(2-pyridyidithio)toluene, sulfosuccinimidyl-6-[a-methyl-a-(pyridyidithiol)-toluamido] hexanoate, N-succinimidyl-3-(-2-pyridyldithio)-proprionate, succinimidyl 6[3(-(-2-pyridyldithio)-proprionamido] hexanoate, sulfosuccinimidyl 6[3(-(-2-pyridyldithio)-propionamido] hexanoate, 3-(2-pyridyldithio)-propionyl hydrazide, Ellman'"'"'s reagent, dichlorotriazinic acid, and S-(2-thiopyridyl)-L-cysteine.