IP Library Patent Application 10895941
Patent Application
App. No. 10/895,941

Use of a chemically stabilized chlorite solution for inhibiting an antigen-specific immune response

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Patent No.
US None
App. No.
10/895,941
Abstract

Methods of using a stabilized chlorite solution to inhibit antigen-specific immune responses are disclosed. The stabilized chlorite solution, when administered to a mammal in need thereof, can prevent the presentation of antigens by antigen presenting cells. The stabilized chlorite solution therefore is useful in treating, inter alia, auto-immune diseases, treating diseases caused by an inappropriate immune response, treating lymphoproliferative disease and in inhibiting rejection in transplant patients.

Claims (21)

1 - 26 . (canceled)

27 . A method of inhibiting a disease or syndrome associated with an inappropriate or unwanted immune response, comprising administering to a patient suffering from said disease a therapeutically effective amount of a composition comprising a stabilized chlorite solution, wherein said solution may be represented by the formula ClO 2 − x nO 2 , wherein n is 0. 1-0.25, and wherein said disease or syndrome is selected from the group consisting of myasthenia gravis, systemic lupus erythematosus, serum disease, type I diabetes, rheumatoid arthritis, juvenile rheumatoid arthritis, rheumatic fever, Sjögren syndrome, systemic sclerosis, spondylarthropathies, Lyme disease, sarcoidosis, autoimmune hemolysis, autoimmune hepatitis, autoimmune neutropenia, autoimmune polyglandular disease, autoimmune thyroid disease, multiple sclerosis, inflammatory bowel disease, colitis, Crohn's disease, and chronic fatigue syndrome.

28 . The method according to claim 27 , wherein said disease or syndrome is systemic lupus erythemotosus.

29 . The method according to claim 27 , wherein said disease or syndrome is organ transplant or graft rejection.

30 . A method of reducing inflammation accompanying a disease or syndrome that induces an inappropriate or unwanted antigen-specific immune response, comprising administering to a patient suffering from said disease or syndrome a therapeutically effective amount of a composition comprising a stabilized chlorite solution, wherein said solution may be represented by the formula ClO 2 − x nO 2 , wherein n is 0.1-0.25, and wherein said disease is selected from the group consisting of hepatitis B, hepatitis C, chronic hepatitis, and chronic obstructive pulmonary disease.

31 . The method according to claim 30 , wherein said disease is hepatitis B.

32 . The method according to claim 30 , wherein said disease is hepatitis C.

33 . The method according to claim 30 , wherein said disease is chronic hepatitis.

34 . The method according to claim 30 , wherein said disease is chronic obstructive pulmonary disease.

35 . A method of treating a lymphoproliferative disease, comprising administering to a human patient suffering from said disease a therapeutically effective amount of a composition comprising a stabilized chlorite solution, wherein said solution may be represented by the formula ClO 2 − x nO 2 , wherein n is 0.1-0.25.

36 . The method according to claim 35 , wherein said lymphoproliferative disease is lymphoma.

37 . A method of inhibiting a disease or syndrome associated with an inappropriate or unwanted immune response, comprising administering to a patient suffering from said disease a therapeutically effective amount of a composition comprising WF 10, wherein said disease or syndrome is selected from the group consisting of myasthenia gravis, systemic lupus erythematosus, serum disease, type I diabetes, rheumatoid arthritis, juvenile rheumatoid arthritis, rheumatic fever, Sjögren syndrome, systemic sclerosis, spondylarthropathies, Lyme disease, sarcoidosis, autoimmune hemolysis, autoimmune hepatitis, autoimmune neutropenia, autoimmune polyglandular disease, autoimmune thyroid disease, multiple sclerosis, inflammatory bowel disease, colitis, Crohn's disease, and chronic fatigue syndrome.

38 . The method according to claim 37 , wherein said disease or syndrome is systemic lupus erythemotosus.

39 . The method according to claim 37 , wherein said disease or syndrome is organ transplant or graft rejection.

40 . A method of reducing inflammation accompanying a disease or syndrome that induces an inappropriate or unwanted antigen-specific immune response, comprising administering to a patient suffering from said disease or syndrome a therapeutically effective amount of a composition comprising WF10, and wherein said disease or syndrome is selected from tne group consisting of hepatitis B, hepatitis C, chronic hepatitis, and chronic obstructive pulmonary disease.

41 . The method according to claim 40 , wherein said disease is hepatitis B.

42 . The method according to claim 40 , wherein said disease is hepatitis C.

43 . The method according to claim 40 , wherein said disease is chronic hepatitis.

44 . The method according to claim 40 , wherein said disease is chronic obstructive pulmonary disease.

45 . A method of treating a lymphoproliferative disease, comprising administering to a human patient suffering from said disease a therapeutically effective amount of a composition comprising WF10.

46 . The method according to claim 47 , wherein said lymphoproliferative disease is lymphoma.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT RECEIVING PARTY PREVIOUSLY RECORDED ON REEL 026594 FRAME 0546. ASSIGNOR CONFIRMS THE CHANGE OF NAME. Recorded Nov 4, 2011
From: DIMETHAID AG
To: NUVO RESEARCH AG
Reel/Frame 027330/0503 →
CHANGE OF NAME Recorded Jul 14, 2011
From: DIMETHAID AG
To: NUVO RESEARCH INC.
Reel/Frame 026594/0546 →