US2020281961A1PendingUtilityA1
Glucocerebroside treatment of disease
Est. expiryFeb 27, 2023(expired)· nominal 20-yr term from priority
A61K 35/17A61K 35/15A61P 31/20A61K 31/7032A61P 31/14A61P 9/00A61P 31/00A61K 31/7004A61K 31/70A61P 3/10A61P 1/04A61K 31/7028A61P 5/00A61P 31/04A61P 27/02A61P 1/16A61K 38/00A61K 38/1709A61P 11/00A61P 7/00A61P 17/00A61P 9/10A61K 31/00A61P 31/12A61P 25/28A61P 37/02A61P 37/04A61P 19/00A61P 3/00A61P 29/00A61P 31/18A61P 35/00A61P 1/00A61K 31/739
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Claims
Abstract
The present invention provides a method for the treatment of immune mediated or immune related diseases or disorders, infectious diseases, metabolic disorders and cancer in mammalian subjects. This method comprises the administration of a naturally occurring, mammalian intermediary metabolite or T cell receptor ligand, preferably a glucosylceramide, to a mammalian subject. In a preferred embodiment, such mammalian subjects are human beings.
Claims
exact text as granted — not AI-modified1 . A method for intrahepatic trapping of CD8+ T-cells in a mammal, comprising:
administering to a mammalian subject a pharmaceutical composition comprising an effective amount of glucocerebroside to intrahepatically trap CD8+ T-cells,
wherein as a result of said administration CD8+ T-cells are intrahepatically trapped.
2 . The method of claim 1 , wherein the mammalian subject is a human subject.
3 . The method of claim 1 , wherein said administering step comprises parenteral administration of said pharmaceutical composition.
4 . The method of claim 3 , wherein the mammalian subject is a human subject.
5 . The method of claim 1 , wherein said administering step comprises intravenous, intraperitoneal, or subcutaneous administration of said pharmaceutical composition.
6 . The method of claim 5 , wherein the mammalian subject is a human subject.
7 . The method of claim 1 , wherein said administering step comprises enteral administration of said pharmaceutical composition.
8 . The method of claim 7 , wherein the mammalian subject is a human subject.
9 . The method of claim 1 , wherein said administering step comprises oral administration of said pharmaceutical composition.
10 . The method of claim 9 , wherein the mammalian subject is a human subject.Cited by (0)
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