Genetically modified porcine cells, tissue, and animals with reduced human xenoreactivity and methods of using the same
US-2024271103-A1 · Aug 15, 2024 · US
US10849841B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10849841-B2 |
| Application number | US-201815894691-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 12, 2018 |
| Priority date | Jun 16, 2006 |
| Publication date | Dec 1, 2020 |
| Grant date | Dec 1, 2020 |
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This invention provides methods of treating androgenetic alopecia (AGA), acne, rosacea, prostate cancer, and benign prostatic hypertrophy (BPH), comprising the step of contacting a subject with a compound or composition capable of decreasing prostaglandin D2 (PGD2) level or activity, a downstream signaling or receptor pathway thereof, or prostaglandin D2 synthase level or activity; methods of stimulating hair growth, comprising the step of contacting a subject with a compound or composition capable of increasing or decreasing the activity or level of a target gene of the present invention, or with a protein product of the target gene or an analogue or mimetic thereof; and methods of testing for AGA and evaluating therapeutic methods thereof, comprising measuring PGD2 levels.
Opening claim text (preview).
What is claimed is: 1. A method of treating androgenetic alopecia (AGA) in a scalp of a subject, comprising the step of orally administering to said subject an effective amount of a compound or composition comprising a prostaglandin D2 antagonist, thereby treating an AGA in a scalp of a subject. 2. The method of claim 1 , further comprising the step of administering to said subject a pro-hair growth prostaglandin selected from a prostaglandin E1, a prostaglandin E2, a prostaglandin F2a; or an analogue thereof. 3. A method of treating androgenetic alopecia (AGA) in a scalp of a subject, comprising the step of orally administering to said subject an effective amount of a prostaglandin (PG) D receptor (DP receptor) antagonist, thereby treating an AGA in a scalp of a subject. 4. The method of claim 1 , wherein said compound or composition decreases a level of a prostaglandin D2 in said scalp. 5. The method of claim 1 , wherein the prostaglandin D2 antagonist is a prostaglandin (PG) D receptor (DP receptor) antagonist. 6. The method of claim 5 , wherein the DP receptor antagonist is a CRTH2 (chemoattractant receptor-homologous molecule expressed on Th2 cells)/DP2 receptor antagonist. 7. The method of claim 3 , wherein the DP receptor antagonist is a CRTH2 (chemoattractant receptor-homologous molecule expressed on Th2 cells)/DP2 receptor antagonist.
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