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US 11,883,459 B2Granted
Thiol isomerases inhibitors for the treatment and prevention of food allergies, allergic diseases, and inflammatory diseases
AssigneeWestern New England University
InventorsDaniel Kennedy, Clinton Mathias
Life of this patent
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Abstract
Disclosed are methods of treating, inhibiting, or preventing the development of, a food allergy in a patient by administering a therapeutically effective amount of a thiol isomerase inhibitor to a patient in need thereof. Also disclosed are methods for treatment of other allergic diseases and inflammatory diseases.
Claims9
A method of treating, inhibiting, or preventing the development of a food allergy in a patient, comprising:
- administering a therapeutically effective amount of two thiol isomerase inhibitors to a patient in need thereof;
- wherein the thiol isomerase inhibitor is a protein disulfide isomerase inhibitor;
- and wherein the thiol isomerase inhibitor is a compound in the class of propynoic acid carbamoyl methyl amides (PACMAs) selected from the group consisting of PACMA 31 (N-(2,4-dimethoxypheny 1)-N-(1-oxo-2- propyn-1-yl)-2-(2-thienyl)glycylglycine ethyl ester);
- juniferdin;
- juniferdin epoxide;
- phenylarsine oxide;
- LOC 14 (2-1 14-(cyclopropylcarbonyl)-1-piperazinyllmethy 11-1,2-benzisothiazol-3(2H)-one);
- CCF 642 (3-(4-methoxypheny 1)-5- 1(5-nitro-2- thienyl)methylene 1-2-thioxo-4-thiazolidinone);
- P1 (N- 1(1,1-dimethylethoxy)carbonyll-L - phenylalanyl1-O -(ethenylsulfonyl1)-N-4-pentyn-1-yl-L-tyrosinamide);
- 1 6F1 6 (2-(2- chloroacety 1)-2,3 ,4,9-tetrahydro-1-methyl-1H-pyrido13,4-blindole-1-carboxylic acid methyl ester);
- ML359 (ethyl 1- (3-chloro-4-hydroxybenzy 1)-4-(2-phenoxyethyl)piperidine-4- carboxylate);
- zafirlukast;
- CGP -13501;
- CGP-7930;
- alosetron;
- balsalazide;
- benserazide;
- butaclamol;
- oxcarbazepine;
- or combination thereof, or a protein disulfide isomerase inhibitor targeting antibody, selected from the group consisting of protein disulfide isomerase inhibitor antibody RL90, or MA3-0 19 and wherein the therapeutically effective amount of the two thiol isomerase inhibitors are formulated as a pharmaceutical composition suitable for administration orally, parenterally, or transdermally.
17 more elements
A method of inhibiting or preventing cytokine production in a patient, the cytokine production caused by a food allergen, the method comprising:
- administering a therapeutically effective amount of two thiol isomerase inhibitors to a patient in need thereof;
- wherein the thiol isomerase inhibitor is a protein disulfide isomerase (PDI) inhibitor;
- and wherein the thiol isomerase inhibitor is a compound in the class of propynoic acid carbamoyl methyl amides (PACMAs) selected from the group consisting of PACMA 31 (N-(2,4-dimethoxypheny 1)-N-(1-oxo-2- propyn-1-yl)-2-(2-thienyl)glycylglycine ethyl ester);
- juniferdin;
- juniferdin epoxide;
- phenylarsine oxide;
- LOC 14 (2-[[4-(cyclopropylcarbonyl)-1-piperazinyllmethy 11-1,2-benzisothiazol-3(2H)-one);
- CCF 642 (3-(4-methoxypheny 1)-5-[(5-nitro-2- thienyl)methylene 1-2-thioxo-4-thiazolidinone);
- P1 (N-[(1,1-dimethylethoxy)carbonyll-L- phenylalanyl1-O-(ethenylsulfonyl1)-N-4-pentyn-1-yl-L -tyrosinamide);
- 1 6F1 6 (2-(2- chloroacety 1)-2,3 ,4,9-tetrahydro-1-methyl- 1H-pyrido[3,4-blindole-1-carboxylic acid methyl ester);
- ML359 (ethyl 1 -(3-chloro-4-hydroxybenzy 1)-4-(2-phenoxyethyl)piperidine-4- carboxylate);
- zafirlukast;
- CGP- 13501;
- CGP-7930;
- alosetron;
- balsalazide;
- benserazide;
- butaclamol;
- oxcarbazepine;
- or combination thereof, or a protein disulfide isomerase inhibitor targeting antibody, selected from the group consisting of protein disulfide isomerase inhibitor antibody RL90, or MA3-0 19, and wherein the therapeutically effective amount of the two thiol isomerase inhibitors is formulated as a pharmaceutical composition suitable for administration orally, parenterally, by inhalation or spray, transdermally, or rectally.
17 more elements
Dependencies are inferred from the claim text.