Gene therapy for recessive dystrophic epidermolysis bullosa using genetically corrected autologous keratinocytes
US-12173314-B2 · Dec 24, 2024 · US
US12357560B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12357560-B2 |
| Application number | US-202318225377-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 24, 2023 |
| Priority date | Nov 30, 2018 |
| Publication date | Jul 15, 2025 |
| Grant date | Jul 15, 2025 |
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The present invention provides a composition for treating or preventing skin pigmentation, which contains fibroblasts as an active ingredient, wherein the fibroblasts are those fibroblasts which are less damaged than fibroblasts localized in a site where the skin pigmentation occurs, and the composition is characterized by being intended to be applied to a site where the pigmentation occurs or a dermis tissue around the site.
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The invention claimed is: 1. A method for treatment of skin pigmentation of a subject in need thereof, the method comprising: applying fibroblasts as an active ingredient to a site of skin pigmentation or a surrounding dermal tissue of the subject, wherein: the fibroblasts are fibroblasts with less damage than fibroblasts localized at the site of skin pigmentation, the fibroblasts have lower expression of a cell senescence marker than fibroblasts localized at the site of skin pigmentation, the fibroblasts are derived from a tissue selected from the group consisting of a gluteal region, an abdominal region, a thorax, a femoral region, an upper arm, a dorsal region, a gingiva, an oral mucosa, a scalp, and an auricle rear, the cell senescence marker is one or more selected from the group consisting of senescent acidic β-galactosidase (SA-βgal), cell cycle check mechanism-associated factor and cell senescence-associated secretory phenotype (SASP) factor, and the skin pigmentation is caused by activated melanocytes induced by photo damaged-fibroblasts. 2. The method according to claim 1 , wherein the pigmentation is from one or more conditions selected from the group consisting of senile pigmentation spots, seborrheic keratosis, Chloasma, freckles and floriform pigmented spots. 3. The method according to claim 1 , wherein the fibroblasts are autologous fibroblasts. 4. The method of claim 1 , wherein the skin pigmentation is caused by overproduction of melanin by melanocytes due to ultraviolet ray exposure.
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