Compositions and methods of therapy

• US 20060233743A1
• Filed: 10/21/2003
• Published: 10/19/2006
• Est. Priority Date: 10/21/2002
• Status: Abandoned Application

• Current Assignee: Medical Research Council (Government of United Kingdom)
• Original Assignee: Medical Research Council (Government of United Kingdom)
• Inventors: Kelly, Rodney William
• Application Number:
  US10/532,291
• Publication Number:
  US 20060233743A1
• Time in Patent Office: Days
• US Class Current: 424/85.100
• CPC Class Codes: A61K 2300/00 Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• CPC Class Codes: A61K 31/5575 having a cyclopentane, e.g. prostaglandin E2, prostaglandin F2-alpha
• 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 38/193 Colony stimulating factors [CSF]
• CPC Class Codes: A61P 1/04 for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
• CPC Class Codes: A61P 1/18 for pancreatic disorders, e.g. pancreatic enzymes
• CPC Class Codes: A61P 11/06 Antiasthmatics
• CPC Class Codes: A61P 17/00 Drugs for dermatological disorders
• CPC Class Codes: A61P 17/12 Keratolytics, e.g. wart or anti-corn preparations
• CPC Class Codes: A61P 19/02 for joint disorders, e.g. arthritis, arthrosis
• CPC Class Codes: A61P 21/04 for myasthenia gravis
• CPC Class Codes: A61P 25/00 Drugs for disorders of the nervous system
• CPC Class Codes: A61P 27/02 Ophthalmic agents
• CPC Class Codes: A61P 29/00 Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• CPC Class Codes: A61P 3/10 for hyperglycaemia, e.g. antidiabetics
• CPC Class Codes: A61P 31/12 Antivirals
• CPC Class Codes: A61P 31/22 for herpes viruses
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: A61P 35/02 specific for leukemia
• CPC Class Codes: A61P 37/00 Drugs for immunological or allergic disorders
• CPC Class Codes: A61P 37/02 : Immunomodulators
• CPC Class Codes: A61P 37/06 : Immunosuppressants, e.g. drugs for graft rejection
• CPC Class Codes: A61P 37/08 : Antiallergic agents antiasthmatic agents A61P11/06; ophthalmic antiallergics A61P27/14
• CPC Class Codes: A61P 43/00 : Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: A61P 5/14 : of the thyroid hormones, e.g. T3, T4
• CPC Class Codes: A61P 7/06 : Antianaemics
• CPC Class Codes: A61P 7/10 : Antioedematous agents; Diuretics
• CPC Class Codes: A61P 9/00 : Drugs for disorders of the cardiovascular system

Abstract

A method of inducing tolerance to an antigen in a patient, the method comprising administering to the patient an agent which raises the effective cAMP concentration in a monocyte cell and GMCSF or a derivative thereof. Preferably, the agent which raises the effective cAMP concentration in a monocyte cell is a prostaglandin or agonist thereof which stimulates cAMP production in a monocyte. Optionally, the antigen to which it is desired to induce tolerance, or a derivative thereof, may also be administered.

Claims

1. A method of inducing tolerance to an antigen in a patient, the method comprising administering to the patient an agent which raises the effective cAMP concentration in a monocyte cell and granulocyte-macrophage colony stimulating factor (GMCSF) or a derivative thereof.

2. A method according to claim 1 wherein the agent which raises the effective cAMP concentration in a monocyte cell is any one or more of a prostaglandin or agonist thereof, a β

-adrenergic agent, a blocker of cAMP export from the cell, forskolin or a derivative thereof, a cAMP phosphodiesterase inhibitor, a cAMP analogue, or cholera toxin or a derivative or fragment thereof.

3. A method according to claim 2 wherein the blocker of cAMP export from the cell is probenicid or progesterone.

4. A method according to claim 2 wherein the cAMP analogue is Sp-adenosine 3′

,5′

-cyclic monophosphorothioate or 8-bromoadenosine 3′

,5′

cyclic monophosphate or dibutryryl cAMP.

5. A method according to claim 2 wherein the prostaglandin or agonist thereof stimulates cAMP production in a monocyte.

6. A method according to claim 2 wherein the prostaglandin or agonist thereof is any one of a prostaglandin E or an analogue thereof, prostaglandin E₂ or an analogue thereof, dinoprostone, gemeprost, misoprostol, alprostadil, limaprost, butaprost, 11-deoxy PGE1, AH23848, AH13205, or a 19-hydroxy PGE.

7. A method according to claim 1 wherein the GMCSF is human GMCSF having the amino acid sequence of SEQ ID NO:

2 or naturally occurring variants thereof.

8. A method according to claim 1 wherein the GMCSF is sargramostim.

9. A method according to claim 1 further comprising administering to the patient one or more of a monocyte chemotactic agent, a phosphodiesterase (PDE) inhibitor, and the antigen or a derivative thereof.

10. A method according to claim 9 wherein the monocyte chemotactic agent is MCP-1 or MIP-1α

.

12. A method according to claim 9 wherein the PDE inhibitor is any one of 3-isobutyl-1-methylxanthine (IBMX), pentoxifylline (3,7-dihydro-3,7-dimethyl-1-(5-oxohexyl)-1H-purine-2,6-dione), rolipram (4-[3-cyclopentyloxy-4-methoxyphenyl]-2-pyrrolidinone), CP80 633, CP102 995, CP76 593, Ro-20-1724 (4-[3-butoxy-4-methoxybenzyl]-2-imidazolidinone), theophylline, or denbufylline (1,3-di-n-butyl-7-(2-oxopropyl)-xanthine).

13. A method according to claim 9 wherein the PDE inhibitor is selective for type IV PDE.

14. A method according to claim 13 wherein the PDE inhibitor selective for type IV PDE is any one of rolipram (4-[3-cyclopentyloxy-4-methoxyphenyl]-2-pyrrolidinone), CP80 633, CP102 995, CP76 593, Ro-20-1724 (4-[3-butoxy-4-methoxybenzyl]-2-imidazolidinone), denbufylline (1,3-di-n-butyl-7-(2-oxopropyl)-xanthine), or CDP840, RP73401 or RS33793.

16. A method according to claim 9 wherein one or more of the agent which raises the effective cAMP concentration in a monocyte cell, the GMCSF or derivative thereof, the monocyte chemotactic agent, the PDE inhibitors and the antigen or derivative thereof is administered (i) locally at a site where tolerance is required, (ii) systemically, (iii) orally, or (iv) as a suppository or capsule.

20. A method according to claim 16 wherein the suppository or capsule has an enteric coating for release of the one or more of the agent which raises the effective cAMP concentration in a monocyte cell, the GMCSF or derivative thereof, the monocyte chemotactic agent, the PDE inhibitor, and the antigen or derivative thereof in the bowel of the patient.

21. A method according to claim 16 wherein at least the GMCSF or derivative thereof is administered subcutaneously or intravenously.

22. A method according to claim 9 wherein any two or more of the agent which raises the effective cAMP concentration in a monocyte cell, the GMCSF or derivative thereof, the monocyte chemotactic agent, the PDE inhibitors and the antigen or derivative thereof are administered simultaneously.

23. A method of combating a disease or condition associated with transplant rejection comprising:

performing the method according to claim 1, wherein said administering is effective to combat a disease or condition associated with transplant rejection.

24. A method according to claim 23 wherein the disease or condition associated with transplant rejection comprises graft versus host disease or host versus graft disease.

25. A method according to claim 23 wherein one or more of the agent which raises the effective cAMP concentration in a monocyte cell, the GMCSF or derivative thereof, a monocyte chemotactic agent, a PDE inhibitor, and the antigen or derivative thereof is administered prior to the transplant.

26. A method according to claim 23 wherein the antigen is HLA-A2.

27. A method of treating an autoimmune disease or condition comprising:

performing the method according to claim 1, wherein said administering is effective to treat an autoimmune disease or condition.

28. A method according to claim 27 wherein the autoimmune disease is selected from the group consisting of primary myxoedema, thyrotoxicosis, pernicious anaemia, autoimmune atrophic gastris, Addison'"'"'s disease, insulin-dependent diabetes mellitus (IDDM), Goodpasture'"'"'s syndrome, myasthenia gravis, sympathetic ophthalmia, multiple sclerosis (MS), autoimmune haemolytic anaemia, idiopathic leucopenia, ulcerative colitis, dermatomyositis, scleroderma, mixed connective tissue disease, rheumatoid arthritis, irritable bowel syndrome, systemic lupus erythromatosus (SLE), Hashimoto'"'"'s disease, thyroiditis, Behcet'"'"'s disease, coeliac disease/dermatitis herpetiformis, renal vasculitis, and demyelinating disease.

29. A method according to claim 27 wherein the antigen is a self-antigen.

30. A method according to claim 27, wherein the autoimmune disease is pernicious anaemia, and the antigen is vitamin B₁₂;

the disease is Addison'"'"'s disease, and the antigen is adrenal antigen;

the disease is IDDM, and the antigen is glutamic acid decarboxylase (GAD), insulin, or IA-2;

the disease is Goodpasture'"'"'s syndrome or renal vasculitis, and the antigen is renal antigen or endothelial antigen;

the disease is myasthenia gravis, and the antigen is the acetyl choline receptor;

the disease is sympathetic ophthalmia, and the antigen is ocular antigen;

the disease is multiple sclerosis (MS), and the antigen is myelin basic protein (MBP), proteolipid protein (PLP), or myelin oligodendrocyte glycoprotein (MOG);

the disease is autoimmune haemolytic anaemia, and the antigen is red cell antigen;

the disease is idiopathic leucopenia, and the antigen is leukocyte antigen;

the disease is ulcerative colitis, and the antigen is a food antigen or a viral antigen;

the disease is dermatomyositis, and the antigen is smooth muscle antigen;

the disease is scleroderma, and the antigen is a connective tissue antigen;

the disease is mixed connective tissue disease, and the antigen is a connective tissue antigen;

the disease is irritable bowel syndrome, and the antigen is a food antigen;

the disease is systemic lupus erythmatosus (SLE), and the antigen is a histone protein or immunoglobulin heavy chain;

the disease is Hashimoto'"'"'s disease, primary myxoedema or thyrotoxicosis, and the antigen is thyroid antigen;

the disease is rheumatoid arthritis, and the antigen is type II collagen or a heat shock protein (HSP);

the disease is thyroiditis, and the antigen is thyroglobulin;

the disease is Behcet'"'"'s disease, and the antigen is Sag, HLA-B44, B51, or HSP65;

the disease is Coeliac disease/Dermatitis herpetiformis, and the antigen is gliadin or the α

fraction thereof;

or the disease is demyelinating disease, and the antigen is myelin.

31. A method of treating an allergic disease or condition in a patient comprising:

performing the method according to claim 1, wherein said administering is effective to treat an allergic disease or condition in the patient.

32. A method according to claim 31 wherein the allergic disease or condition is allergic asthma.

33. A method according to claim 31, wherein the antigen is a mite allergen, a dust allergen, a cat allergen, a dog allergen or a horse allergen.

34. A method according to claim 1, wherein the induced tolerance to the antigen is effective to treat an aberrant or undesired immune or inflammatory response to the antigen in the patient.

35. A method according to claim 34 wherein the aberrant or undesired immune or inflammatory response involves a deficiency in IL-10 production.

11. (canceled)

15. (canceled)

17-19. -19. (canceled)

36. A composition comprising an agent which raises the effective cAMP concentration in a monocyte cell and granulocyte-macrophage colony stimulating factor (GMCSF) or a derivative thereof.

37. A composition according to claim 36 wherein the agent which raises the effective cAMP concentration in a monocyte cell is any one or more of a prostaglandin or agonist thereof, a β

-adrenergic agent, a blocker of cAMP export from the cell, forskolin or a derivative thereof, a cAMP phosphodiesterase inhibitor, a cAMP analogue, or cholera toxin or a derivative or fragment thereof.

38. A composition according to claim 37 wherein the blocker of cAMP export from the cell is probenicid or progesterone.

39. A composition according to claim 37 wherein the cAMP analogue is Sp-adenosine 3′

,5′

-cyclic monophosphorothioate or 8-bromoadenosine 3′

,5′

cyclic monophosphate.

40. A composition according to claim 37 wherein the prostaglandin or agonist thereof stimulates cAMP production in a monocyte.

41. A composition according to claim 37 wherein the prostaglandin or agonist thereof is a prostaglandin E or an analogue thereof, prostaglandin E₂ or an analogue thereof, dinoprostone, gemeprost, misoprostol, alprostadil, limaprost, butaprost, 11-deoxy PGE1, AH23848, AH13205, or a 19-hydroxy PGE.

42. A composition according to claim 36 wherein the GMCSF is human GMCSF having the amino acid sequence of SEQ ID NO:

2 or naturally occurring variants thereof.

43. A composition according to claim 36 wherein the GMCSF is sargramostim.

44. A composition according to claim 36 further comprising one or more of a monocyte chemotactic agent, a phosphodiesterase (PDE) inhibitor, and an antigen or derivative thereof.

45. A composition according to claim 44 wherein the monocyte chemotactic agent is MCP-1 or MIP-1α

.

47. A composition according to claim 44 wherein the PDE inhibitor is any one of 3-isobutyl-1-methylxanthine (IBMX), pentoxifylline (3,7-dihydro-3,7-dimethyl-1-(5-oxohexyl)-1H-purine-2,6-dione), rolipram (4-[3-cyclopentyloxy-4-methoxyphenyl]-2-pyrrolidinone), CP80 633, CP102 995, CP76 593, Ro-20-1724 (4-[3-butoxy-4-methoxybenzyl]-2-imidazolidinone), theophylline, or denbufylline (1,3-di-n-butyl-7-(2-oxopropyl)-xanthine).

48. A composition according to claim 44 wherein the PDE inhibitor is selective for type IV PDE.

49. A composition according to claim 48 wherein the PDE inhibitor selective for type IV PDE is any one of rolipram (4-[3-cyclopentyloxy-4-methoxyphenyl]-2-pyrrolidinone), CP80 633, CP102 995, CP76 593, Ro-20-1724 (4-[3-butoxy-4-methoxybenzyl]-2-imidazolidinone), denbufylline (1,3-di-n-butyl-7-(2-oxopropyl)-xanthine), or CDP840, RP73401 or RS33793.

51. A pharmaceutical composition comprising the composition according to claim 36 and a pharmaceutically acceptable carrier, diluent or excipient.

46. (canceled)

50. (canceled)

52-65. -65. (canceled)

66. A therapeutic system for inducing tolerance to an antigen in a patient, the system comprising an agent which raises the effective cAMP concentration in a monocyte cell and GMCSF or a derivative thereof.

67. A therapeutic system according to claim 66 further comprising one or more of the antigen, a monocyte chemotactic agent, and a phosphodiesterase (PDE) inhibitor.

69. A therapeutic system according to claim 67 wherein one or more of the agent which raises the effective cAMP concentration in a monocyte cell, the GMCSF or derivative thereof, the monocyte chemotactic agent, the PDE inhibitor, and the antigen or derivative thereof is in a preparation for (i) administration locally at a site where tolerance is required, (ii) systemic administration, (iii) oral administration, or (iv) administration as a suppository or capsule.

73. A method of stimulating or enhancing granulysin expression in cells of a macrophage/monocyte lineage comprising administering to the cells a therapeutic system according to claim 66.

74. A method of treating a viral infection in a patient comprising administering to the patient a therapeutic system according to claim 66.

75. A method according to claim 74 wherein the viral infection is a herpes simplex virus infection or a human papilloma virus infection.

78. A method of stimulating or enhancing IL-10 expression in, and secretion from, cells of a macrophage/monocyte lineage comprising administering to the cells a therapeutic system according to claim 66.

79. A method of treating a tumour in a patient comprising administering to the patient a therapeutic system according to claim 66.

68. (canceled)

70-72. -72. (canceled)

76-77. -77. (canceled)

80-81. -81. (canceled)