Macrocyclic peptidomimetic protease inhibitor and use thereof
US-2024327458-A1 · Oct 3, 2024 · US
US10076491B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10076491-B2 |
| Application number | US-201414166965-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 29, 2014 |
| Priority date | Feb 5, 2013 |
| Publication date | Sep 18, 2018 |
| Grant date | Sep 18, 2018 |
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The invention provides a vaccine composition containing an antigen for inducing cellular immunity, comprising at least one first cellular immunity induction promoter.
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What is claimed is: 1. A method for inducing cellular immunity in a subject, comprising transdermally administering, to intact skin or under mildly irritating conditions, an immunogenic composition comprising: an antigen, at least one first cellular immunity induction promoter selected from the group consisting of a cyclooxygenase inhibitor, a prostaglandin receptor antagonist, a prostaglandin receptor agonist, a TSLP production inhibitor, an adenylate cyclase inhibitor, an omega-3 fatty acid, a PPAR agonist, a dopamine receptor antagonist, a dopamine receptor agonist, a histamine receptor agonist, a histamine receptor antagonist, a serotonin receptor agonist, a serotonin receptor antagonist, a vasopressin receptor antagonist, a vasopressin receptor agonist, a muscarine receptor antagonist, a muscarine receptor agonist, an adrenergic receptor antagonist, an adrenergic receptor agonist, an angiotensin receptor agonist, a GABA receptor agonist, a thrombin receptor antagonist, a thrombin receptor agonist, an opioid receptor agonist, an ADP receptor agonist, a leukotriene receptor antagonist, a leukotriene receptor agonist, a melatonin receptor agonist, a somatostatin receptor agonist, a cannabinoid receptor agonist, a sphingosine-1 phosphate receptor agonist, a metabotropic glutamate receptor agonist, a phospholipase A2 inhibitor, a TGF-β production inhibitor, and a Th2 cytokine inhibitor, and a TLR ligand other than a TLR9 ligand. 2. The method according to claim 1 , wherein the composition is administered to the skin under a mildly irritating condition. 3. The method according to claim 2 , wherein the mildly irritating condition is a condition under which transepidermal water loss (TEWL) in a model animal for skin irritation evaluation before the administration of the composition is 50 g/hm 2 or less. 4. The method according to claim 2 , wherein the mildly irritating condition is a condition under which the cutaneous TSLP level in a model animal for skin irritation evaluation at completion of the administration of the composition is 10000 pg/mg protein or less. 5. The method according to claim 1 , wherein the method is for the treatment of a cancer. 6. The method according to claim 1 , wherein the method is for the treatment of a viral disease. 7. The method according to claim 1 , wherein the TLR ligand is a TLR4 ligand. 8. The method according to claim 7 , wherein the TLR4 ligand is a lipopolysaccharide (LPS) derived from bacteria or plants. 9. The method according to claim 8 , wherein the TLR4 ligand is a lipopolysaccharide (LPS) derived from Pantoea genus. 10. The method according to claim 1 , wherein the TLR ligand is a TLR7 and/or TLR8 ligand. 11. The method according to claim 10 , wherein the TLR7 and/or TLR8 ligand is imiquimod. 12. The method according to claim 1 , wherein the first cellular immunity induction promoter is a cyclooxygenase inhibitor. 13. The method according to claim 12 , wherein the cyclooxygenase inhibitor is selected from etodolac, loxoprofen, indomethacin, aspirin, diclofenac, ketoprofen, celecoxib, valdecoxib, and derivatives thereof, and pharmacologically acceptable salts thereof. 14. The method according to claim 12 , wherein the cyclooxygenase inhibitor is loxoprofen. 15. The method according to claim 11 , wherein the cyclooxygenase inhibitor is loxoprofen.
Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title
Antineoplastic agents · CPC title
Drugs for immunological or allergic disorders · CPC title
Immunostimulants · CPC title
characterised by the route of administration · CPC title
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