Methods for treating conditions associated with lectin-dependent complement activation

• US 20060018896A1
• Filed: 06/09/2005
• Published: 01/26/2006
• Est. Priority Date: 06/10/2004
• Status: Abandoned Application

• Current Assignee: Omeros Corporation, University of Leicester
• Original Assignee: Omeros Corporation, University of Leicester
• Inventors: Parent, James B., Schwaeble, Hans-Wilhelm, Tedford, Clark E., Fujita, Teizo, Stover, Cordula Margaret
• Application Number:
  US11/150,887
• Publication Number:
  US 20060018896A1
• Time in Patent Office: Days
• US Class Current: 424/130.100
• CPC Class Codes: A61K 2039/505 comprising antibodies
• CPC Class Codes: A61K 38/1732 Lectins
• CPC Class Codes: A61K 38/482 Serine endopeptidases (3.4.21)
• CPC Class Codes: A61P 31/00 Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
• CPC Class Codes: C07K 14/4703 Inhibitors; Suppressors
• CPC Class Codes: C07K 16/40 against enzymes
• CPC Class Codes: C07K 2317/21 from primates, e.g. man
• CPC Class Codes: C07K 2317/24 containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
• CPC Class Codes: C07K 2317/55 Fab or Fab'
• CPC Class Codes: C12Y 304/21104 Mannan-binding lectin-associated serine protease-2 (3.4.21.104)

Abstract

In one aspect, the invention provides methods of inhibiting the effects of lectin-dependent complement activation in a living subject. The methods comprise the step of administering, to a subject in need thereof, an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation. In some embodiments, the MAp19 inhibitory agent inhibits cellular injury associated with lectin-mediated complement pathway activation, while leaving the classical (C1q-dependent) pathway component of the immune system intact. In another aspect, the invention provides MAp19 specific antibodies that do not bind to MASP-2 and methods of producing MAp19 specific antibodies. In another aspect, the invention provides compositions for inhibiting the effects of lectin-dependent complement activation, comprising a therapeutically effective amount of a MAp19 inhibitory agent and a pharmaceutically acceptable carrier.

Claims

1. A method of inhibiting lectin-dependent complement activation in a subject in need thereof, comprising administering to the subject an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

2. The method of claim 1 wherein the MAp19 inhibitory agent inhibits a protein complex comprising one or more MAp19 polypeptides.

3. The method of claim 1 wherein the MAp19 inhibitory agent specifically binds to a polypeptide comprising SEQ ID NO:

3.

4. The method of claim 3 wherein the MAp19 inhibitory agent specifically binds to a polypeptide comprising SEQ ID NO:

3 with an affinity of at least 10 times greater than it binds to other antigens in the complement system.

5. The method of claim 3 wherein the MAp19 inhibitory agent specifically binds to the polypeptide at a location within amino acid residues 160 to 170 of SEQ ID NO:

3.

6. The method of claim 5 wherein the MAp19 inhibitory agent is selected from the group consisting of an antibody or fragment thereof, a polypeptide, a peptide, and a non-peptide agent.

7. The method of claim 6 wherein the MAp19 inhibitory agent is an antibody or fragment thereof that specifically binds to a portion of SEQ ID NO:

3.

8. The method of claim 7 wherein the antibody or fragment thereof is monoclonal.

9. The method of claim 8 wherein the anti-MAp19 antibody or fragment thereof does not bind to MASP-2.

10. The method of claim 9 wherein the anti-MAp19 antibody is produced in a MAp19 deficient transgenic animal.

11. The method of claim 8 wherein the antibody is a chimeric, humanized or human antibody.

12. The method of claim 6 wherein the MAp19 inhibitory agent is a peptide derived from a polypeptide selected from the group consisting of human MASP-2, human MAp19, human MASP-1 that inhibits MAp19, human MBL that inhibits MAp19, human H-ficolin that inhibits MAp19, human M-ficolin, and human L-ficolin that inhibits MAp19.

13. The method of claim 6 wherein the MAp19 inhibitory agent is a non-peptide agent that specifically binds to a polypeptide comprising SEQ ID NO:

3.

14. A method of inhibiting lectin-dependent complement activation in a subject in need thereof, comprising administering to the subject an amount of a MAp19 inhibitory agent effective to selectively inhibit lectin complement activation without substantially inhibiting C1q-dependent complement activation.

15. An anti-MAp19 antibody that does not bind to MASP-2.

16. The anti-MAp19 antibody of claim 15, wherein the antibody is monoclonal.

17. The anti-MAp19 antibody of claim 16 wherein the antibody inhibits lectin-dependent complement activation as measured in an in vitro assay.

18. A method of producing an anti-human MAp19 antibody that does not cross-react with human MASP-2 comprising generating a murine MAp19 deficient transgenic animal, integrating a human MASP-2 transgene into said murine MAp19 deficient animal, introducing a human MAp19 antigen into said animal, and selecting anti-human MAp19 antibodies that do not bind to human MASP-2.

19. The method of claim 18, further comprising the step of producing a monoclonal antibody.

20. An antibody obtained by the method of claim 18 or 19.

21. A composition for inhibiting lectin-dependent complement activation comprising a therapeutically effective amount of a MAp19 inhibitory agent and a pharmaceutically acceptable carrier.

22. A method of manufacturing a medicament for use in inhibiting the effects of lectin-dependent complement activation in living subjects in need thereof, comprising combining a therapeutically effective amount of a MAp19 inhibitory agent in a pharmaceutical carrier.

23. A method for treating a patient deficient in MAp19 by administering to the patient a polypeptide comprising SEQ ID NO:

3, or a portion thereof.

24. A method of treating a subject suffering from a lectin-dependent complement mediated vascular condition comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

25. The method of claim 24 wherein the vascular condition is selected from the group consisting of a cardiovascular condition, a cerebrovascular condition, a peripheral (e.g., musculoskeletal) vascular condition, a renovascular condition, a mesenteric/enteric vascular condition, revascularization to transplants and/or replants, vasculitis, Henoch-Schonlein purpura nephritis, systemic lupus erythematosus-associated vasculitis, vasculitis associated with rheumatoid arthritis, immune complex vasculitis, Takayasu'"'"'s disease, dilated cardiomyopathy, diabetic angiopathy, Kawasaki'"'"'s disease (arteritis), venous gas embolus (VGE), and restenosis following stent placement, rotational atherectomy and percutaneous transluminal coronary angioplasty (PTCA).

26. A method of treating a subject suffering from a lectin-dependent complement mediated condition associated with an ischemia-reperfusion injury comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

27. The method of claim 26 wherein the ischemia-reperfusion injury is associated with aortic aneurysm repair, cardiopulmonary bypass, vascular reanastomosis in connection with organ transplants and/or extremity/digit replantation, stroke, myocardial infarction, and hemodynamic resuscitation following shock and/or surgical procedures.

28. A method of treating and/or preventing atherosclerosis in a subject in need thereof, comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

29. A method of treating a subject suffering from a lectin-dependent complement mediated condition associated with an inflammatory gastrointestinal disorder comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

30. The method of claim 29 wherein the inflammatory gastrointestinal disorder is selected from the group consisting of pancreatitis, Crohn'"'"'s disease, ulcerative colitis, irritable bowel syndrome and diverticulitis.

31. A method of treating a subject suffering from a lectin-dependent complement mediated pulmonary condition comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

32. The method of claim 31 wherein the pulmonary condition is selected from the group consisting of acute respiratory distress syndrome, transfusion-related acute lung injury, ischemia/reperfusion acute lung injury, chronic obstructive pulmonary disease, asthma, Wegener'"'"'s granulomatosis, antiglomerular basement membrane disease (Goodpasture'"'"'s disease), meconium aspiration syndrome, bronchiolitis obliterans syndrome, idiopathic pulmonary fibrosis, acute lung injury secondary to burn, non-cardiogenic pulmonary edema, transfusion-related respiratory depression and emphysema.

33. A method of inhibiting lectin-dependent complement activation in a subject that has undergone, is undergoing, or will undergo an extracorporeal reperfusion procedure comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

34. The method of claim 33 wherein the extracorporeal reperfusion procedure is selected from the group consisting of hemodialysis, plasmapheresis, leukopheresis, extracorporeal membrane oxygenator (ECMO), heparin-induced extracorporeal membrane oxygenation LDL precipitation (HELP) and cardiopulmonary bypass (CPB).

35. A method of treating a subject suffering from a lectin-dependent complement mediated musculoskeletal condition comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

36. The method of claim 35 wherein the musculoskeletal condition is selected from the group consisting of osteoarthritis, rheumatoid arthritis, gout, neuropathic arthropathy, psoriatic arthritis, juvenile rheumatoid arthritis, spondyloarthropathy, crystalline arthropathy and systemic lupus erythematosus (SLE).

37. A method of treating a subject suffering from a lectin-dependent complement mediated renal condition comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

38. The method of claim 37 wherein the renal condition is selected from the group consisting of mesangioproliferative glomerulonephritis, membranous glomerulonephritis, membranoproliferative glomerulonephritis (mesangiocapillary glomerulonephritis), acute postinfectious glomerulonephritis (poststreptococcal glomerulonephritis), cryoglobulinemic glomerulonephritis, lupus nephritis, Henoch-Schonlein purpura nephritis and IgA nephropathy.

39. A method of treating a subject suffering from a lectin-dependent complement mediated skin condition comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

40. The method of claim 39 wherein the skin condition is selected from the group consisting of psoriasis, autoimmune bullous dermatoses, eosinophilic spongiosis, bullous pemphigoid, epidermolysis bullosa acquisita, herpes gestationis, thermal burn injury and chemical burn injury.

41. A method of inhibiting lectin-dependent complement activation in a subject that has undergone, is undergoing, or will undergo an organ or tissue transplant procedure comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

42. The method of claim 41 wherein the transplant procedure is selected from the group consisting of organ allotransplantation, organ xenotransplantation organ and tissue graft.

43. A method of treating a subject suffering from a lectin-dependent complement mediated condition associated with a nervous system disorder or injury comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

44. The method of claim 43 wherein the nervous system disorder or injury is selected from the group consisting of multiple sclerosis, myasthenia gravis, Huntington'"'"'s disease, amyotrophic lateral sclerosis, Guillain Barre syndrome, reperfusion following stroke, degenerative discs, cerebral trauma, Parkinson'"'"'s disease, Alzheimer'"'"'s disease, Miller-Fisher syndrome, cerebral trauma and/or hemorrhage, demyellination and meningitis.

45. A method of treating a subject suffering from a lectin-dependent complement mediated condition associated with a blood disorder comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

46. The method of claim 45 wherein the blood disorder is selected from the group consisting of sepsis, severe sepsis, septic shock, acute respiratory distress syndrome resulting from sepsis, systemic inflammatory response syndrome, hemorrhagic shock, hemolytic anemia, autoimmune thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.

47. A method of treating a subject suffering from a lectin-dependent complement mediated condition associated with a urogenital condition comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

48. The method of claim 47 wherein the urogenital condition is selected from the group consisting of painful bladder disease, sensory bladder disease, chronic abacterial cystitis, interstitial cystitis, infertility, placental dysfunction and miscarriage and pre-eclampsia.

49. A method of treating a subject suffering from a lectin-dependent complement mediated condition associated with nonobese diabetes (Type-1 diabetes or Insulin-dependent diabetes mellitus) and/or complications associated with Type-1 or Type-2 (adult onset) diabetes comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

50. The method of claim 49 wherein the complication associated with Type 1 or Type 2 diabetes is selected from the group consisting of angiopathy, neuropathy and retinopathy.

51. A method of inhibiting lectin-dependent complement activation in a subject that has undergone, is undergoing, or will undergo chemotherapeutic treatment and/or radiation therapy comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

52. A method of treating a subject suffering from a malignancy comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

53. A method of treating a subject suffering from an endocrine disorder comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

54. The method of claim 53 wherein the endocrine disorder is selected from the group consisting of Hashimoto'"'"'s thyroiditis, stress, anxiety and hormonal disorders involving regulated release of prolactin, growth or other insulin-like growth factor and adrenocorticotropin from the pituitary.

55. A method of treating a subject suffering from a complement mediated ophthalmologic condition comprising administering an amount of a MAp19 inhibitory agent effective to inhibit lectin-dependent complement activation.

56. The method of claim 55 wherein the ophthalmologic condition is age-related macular degeneration.