US2009136427A1PendingUtilityA1
LIGHT Inhibitors For Asthma, Lung and Airway Inflammation, Respiratory, Interstitial, Pulmonary and Fibrotic Disease Treatment
Assignee: JOLLA INST ALLERGY IMMUNOLOGPriority: Sep 18, 2007Filed: Sep 18, 2008Published: May 28, 2009
Est. expirySep 18, 2027(~1.2 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 31/16A61P 37/08A61P 9/12A61P 29/00A61P 11/02A61P 11/00A61P 11/14A61P 11/08A61P 1/00A61P 17/00A61P 11/06A61K 45/06C07K 2317/76A61K 38/191A61K 31/00C07K 16/2875A61K 39/3955C07K 2319/70A61K 49/0004A61K 2039/505C07K 2317/21C07K 2317/24A61K 9/007
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Claims
Abstract
Methods of treating inflammatory conditions, disease and disorders are provided. Method include, for example, contacting or administering a sufficient amount of a LIGHT inhibitor to a subject to treat the inflammatory condition, disease or disorder.
Claims
exact text as granted — not AI-modified1 . A method for reducing or inhibiting lung or airway inflammation, comprising administering a sufficient amount of an inhibitor of LIGHT (p30 polypeptide) to a subject in need thereof to reduce or inhibit lung or airway inflammation in the subject.
2 . (canceled)
3 . A method for treating asthma, comprising administering a sufficient amount of an inhibitor of LIGHT (p30 polypeptide) to a subject in need thereof to treat asthma.
4 . A method for treating a respiratory disease or disorder, comprising administering a sufficient amount of an inhibitor of LIGHT (p30 polypeptide) to a subject in need thereof to treat the respiratory disease or disorder.
5 . A method for treating an interstitial or pulmonary disease or disorder, comprising administering a sufficient amount of an inhibitor of LIGHT (p30 polypeptide) to a subject to treat the interstitial or pulmonary disease or disorder.
6 . A method for treating a fibrotic disease or disorder, comprising administering a sufficient amount of an inhibitor of LIGHT (p30 polypeptide) to a subject to treat the fibrotic disease or disorder.
7 . The method of claim 4 , wherein the respiratory disease or disorder affects the upper or lower respiratory tract.
8 . The method of claim 4 , wherein the respiratory disease or disorder comprises asthma, allergic asthma, bronchiolitis or pleuritis.
9 . The method of claim 4 , wherein the respiratory disease comprises an allergic disorder.
10 . The method of claim 9 , wherein the allergic disorder is selected from: Extrinsic bronchial asthma; Allergic rhinitis; Onchocercal dermatitis; Atopic dermatitis, Drug reactions; Nodules, eosinophilia, rheumatism, dermatitis, and swelling (NERDS); Eosophageal and a gastrointestinal allergy.
11 . The method of claim 4 , wherein the respiratory disease or disorder is selected from: Airway Obstruction, Apnea, Asbestosis, Atelectasis, Berylliosis, Bronchiectasis, Bronchiolitis, Bronchiolitis Obliterans Organizing Pneumonia, Bronchitis, Bronchopulmonary Dysplasia, Common Cold, Cough, Empyema, Pleural Empyema, Pleural Epiglottitis, Hemoptysis, Hypertension, Kartagener Syndrome, Meconium Aspiration, Pleural Effusion, Pleurisy, Pneumonia, Pneumothorax, Respiratory Distress Syndrome, Respiratory Hypersensitivity, Respiratory Tract Infections, Rhinoscleroma, Scimitar Syndrome, Severe Acute Respiratory Syndrome, Silicosis, Tracheal Stenosis, Whooping Cough and Influenza.
12 . The method of claim 5 , wherein the interstitial or pulmonary disease or disorder, or the fibrotic disease or disorder, is selected from: Eosinophilic pleural effusions; Transient pulmonary eosinophilic infiltrates (Löffler); Histiocytosis; Chronic eosinophilic pneumonia; Hypersensitivity pneumonitis; Allergic bronchopulmonary aspergillosis; Sarcoidosis; Idiopathic pulmonary fibrosis; pulmonary edema; pulmonary embolism; pulmonary emphysema; Pulmonary Hyperventilation; Pulmonary Alveolar Proteinosis; Chronic Obstructive Pulmonary Disease (COPD); Interstitial Lung Disease; and Topical eosinophilia.
13 . The method of any of claims 1 to 12 , wherein treatment reduces, decreases, inhibits, delays, eliminates or prevents the probability, severity, frequency, or duration of one or more symptoms associated with or caused by the lung or airway inflammation, asthma or respiratory, interstitial, or pulmonary disease or disorder, or fibrotic disease or disorder.
14 . The method of any of claims 1 to 12 , wherein one or more symptoms of the lung or airway inflammation, asthma or respiratory, interstitial, or pulmonary disease or disorder, or the fibrotic disease or disorder, is reduced, inhibited, abrogated, eliminated or reversed.
15 . The method of claim 14 , wherein the symptom comprises shortness of breath (dyspnea), wheezing, stridor, coughing, airway remodeling, rapid breathing (tachypnea), prolonged expiration, runny nose, rapid or increased heart rate (tachycardia), rhonchous lung, over-inflation of the chest or chest-tightness, decreased lung capacity, an acute asthmatic episode, or lung, airway or respiratory mucosum inflammation or tissue damage.
16 . The method of claim 14 , wherein the symptom comprises infiltration of eosinophils in lung, lung draining lymph nodes or airway, leukocyte infiltration of lung draining lymph nodes or airway, hyperplasia of mucus secreting epithelium, inflammatory lesion of lung, goblet cell hyperplasia, or increased Th2 cytokine production.
17 . The method of claim 16 , wherein the Th2 cytokine is an interleukin (IL).
18 . The method of claim 17 , wherein the interleukin (IL) comprises IL-4, IL-5, IL-9, IL-13, IL-16, IL-17 or IL-25.
19 . The method of any of claims 1 to 12 , wherein the method reduces or inhibits progression, severity, frequency, duration or probability of a symptom of the lung or airway inflammation, asthma or respiratory, interstitial, or pulmonary disease or disorder, or fibrotic disease or disorder.
20 . The method of claims 1 to 6 , wherein the lung or airway inflammation, asthma or respiratory, interstitial, or pulmonary disease or disorder, or fibrotic disease or disorder, is caused by an allergen or by exercise.
21 . The method of claims 1 to 6 , wherein the lung or airway inflammation, asthma or respiratory, interstitial, or pulmonary disease or disorder, or fibrotic disease or disorder, is chronic or acute.
22 . A method for reducing or inhibiting a Th2-inflammatory response, comprising administering a sufficient amount of an inhibitor of LIGHT (p30 polypeptide) to a subject to reduce or inhibit Th2-inflammatory response.
23 . The method of claim 22 , wherein the Th2-inflammatory response affects an organ or tissue of a subject.
24 . A method of reducing or decreasing the probability, severity, frequency, duration or preventing a subject from having an acute asthmatic episode, comprising administering to a subject that has previously experienced an asthmatic episode or has been diagnosed as having asthma an amount of an inhibitor of LIGHT (p30 polypeptide) to reduce or decrease the probability, severity, frequency, duration or prevent an acute asthmatic episode.
25 . The method of claim 24 , wherein the acute asthmatic episode is caused by or associated with allergic asthma.
26 .- 27 . (canceled)
28 . The method of any of claims 1 to 6 , 22 , 24 , 26 and 27 , wherein the inhibitor of LIGHT (p30 polypeptide) comprises an antibody or subsequence thereof that binds to LIGHT (p30 polypeptide), an antibody or subsequence thereof that binds to HVEM (herpesvirus entry mediator), or an antibody or subsequence thereof that binds to LTβR (lymphotoxin beta receptor).
29 . The method of claim 28 , wherein the antibody is human or humanized.
30 . The method of any of claims 1 to 6 , 22 , 24 , 26 and 27 , wherein the inhibitor of LIGHT (p30 polypeptide) comprises an LTβR (lymphotoxin beta receptor), HVEM or LIGHT polypeptide subsequence, variant sequence, chimeric sequence or dominant negative sequence.
31 . The method of claim 30 , wherein the chimeric sequence comprises a fusion of an LTβR or HVEM polypeptide sequence and an immunoglobulin sequence.
32 . The method of any of claims 1 to 6 , 22 , 24 , 26 and 27 , wherein the subject is a mammal.
33 . The method of any of claims 1 to 6 , 22 , 24 , 26 and 27 , wherein the subject is a human.
34 . The method of any of claims 1 to 6 , wherein the method reduces or decreases undesirable or abnormal eosinophil migration, chemotaxis or generation.
35 .- 38 . (canceled)
39 . The method of any of claims 1 to 6 , 22 , 24 , 26 and 27 , wherein the inhibitor of LIGHT (p30 polypeptide) is administered via inhalation.
40 . The method of any of claims 1 to 6 , 22 , 24 , 26 and 27 , wherein the inhibitor of LIGHT (p30 polypeptide) is formulated into an aerosol.
41 .- 44 . (canceled)
45 . The method of any of claims 1 to 6 , 22 , 24 , 26 and 27 , wherein the inhibitor of LIGHT (p30 polypeptide) is delivered to the lung or airways.
46 . A method of identifying an agent that reduces or inhibits lung or airway inflammation, comprising:
a) administering a test inhibitor of LIGHT (p30 polypeptide) to a subject; and b) measuring lung or airway inflammation in the subject, wherein a reduction or inhibition of lung or airway inflammation identifies the test inhibitor as an agent that reduces or inhibits lung or airway inflammation.
47 . A method of identifying an agent for treating asthma, comprising:
a) administering a test inhibitor of LIGHT (p30 polypeptide) to a subject; and b) measuring a symptom of asthma in the subject, wherein a reduction or inhibition of a symptom of asthma identifies the test inhibitor as an agent for treating asthma.
48 . A method of identifying an agent for treating fibrosis, comprising:
a) administering a test inhibitor of LIGHT (p30 polypeptide) to a subject; and b) measuring a symptom of fibrosis in the subject, wherein a reduction or inhibition of a symptom of fibrosis identifies the test inhibitor as an agent for treating fibrosis.Join the waitlist — get patent alerts
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