US2005059589A1PendingUtilityA1
Methods and compositions for treating allergic reactions
Priority: Oct 15, 1991Filed: Dec 2, 2003Published: Mar 17, 2005
Est. expiryOct 15, 2011(expired)· nominal 20-yr term from priority
Inventors:Michael F. Mullarkey
A61P 37/08A61K 31/573A61P 29/00A61K 38/1793
48
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Claims
Abstract
Methods and compositions for treating allergic reactions, including cutaneous, ocular, nasal and bronchial allergic disease, are disclosed. Interleukin-1 and Tumor Necrosis Factor receptors, and analogues thereof, are employed which bind the respective effector competitively and thereby suppress allergic reactions.
Claims
exact text as granted — not AI-modified1 . A method for treating allergic responses comprising contacting inflamed tissue with a preparation comprising at least one member selected from the group consisting of IL-1 receptors, TNF receptors, and receptor analogues thereof which are capable of binding either IL-1 or TNF.
2 . The method of claim 1 , wherein a substantial portion of the receptors or analogues contained in the preparation are soluble.
3 . The method of claim 1 , wherein said preparation comprises a mixture of IL-1 receptors and TNF receptors.
4 . The method of claim 3 , wherein at least a portion of said TNF receptors are covalently bound to said IL-1 receptors.
5 . The method of claim 3 , wherein at least a portion of said receptor analogues are hybrid fusion molecules comprising a TNF receptor moiety and an IL-1 receptor moiety.
6 . The method of claim 1 , wherein the preparation further comprises a therapeutically effective amount of at least one corticosteroid.
7 . The method of claim 5 , wherein at least a portion of said corticosteroids are covalently bound to said IL-1 receptors.
8 . The method of claim 1 , wherein the tissue to be treated is selected from the group consisting of nasal tissue, ocular tissue, lung tissue, and skin.
9 . A method for testing pharmaceuticals for anti-allergic properties, comprising:
a) providing a test solution comprising at least one challenging allergen; b) providing a pharmaceutical to be tested; c) adding said pharmaceutical to said test solution to make a test mixture; d) injecting one or more individuals interdermally with said test mixture; and e) examining the injection site at intervals after said injecting to determine the extent of an allergic reaction.
10 . The method of claim 9 , wherein said individuals have previously displayed a dual allergic response (early and late) to intradermal challenge with said allergen.
11 . The method of claim 9 , wherein said examining step comprises measuring the area of the wheal reaction on the skin of the individuals.
12 . A therapeutic composition for treating allergic responses comprising at least one member selected from the group consisting of IL-1 receptors, TNF receptors, and receptor analogues thereof which are capable of binding either IL-1 or TNF, together with a pharmaceutically acceptable carrier adapted for topical or parenteral application to a host in need of such treatment.
13 . The therapeutic composition of claim 12 , wherein a substantial portion of the receptors or analogues contained in the preparation are soluble.
14 . The therapeutic composition of claim 12 , wherein said preparation comprises a mixture of IL-1 receptors and TNF receptors.
15 . The therapeutic composition of claim 14 , wherein at least a portion of said TNF receptors are covalently bound to said IL-1 receptors.
16 . The therapeutic composition of claim 14 , wherein at least a portion of said receptor analogues are hybrid fusion molecules comprising a TNF receptor moiety and an IL-1 receptor moiety.
17 . The therapeutic composition of claim 12 , wherein the preparation further comprises a therapeutically effective amount of at least one corticosteroid.
18 . The therapeutic composition of claim 17 , wherein at least a portion of said corticosteroids are covalently bound to said IL-1 receptors.Join the waitlist — get patent alerts
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