Modulation of sphingosine 1-phosphate metabolizing enzymes for the treatment of negative-strand RNA virus infections

Patent metadata

Field	Value
Publication number	US-9687477-B2
Application number	US-201214122399-A
Country	US
Kind code	B2
Filing date	May 31, 2012
Priority date	Jun 1, 2011
Publication date	Jun 27, 2017
Grant date	Jun 27, 2017

Abstract

The present invention relates to compounds and methods for the prevention or treatment of infections by negative strand RNA viruses, such as influenza virus and measles virus, wherein said compounds delay or inhibit viral replication by modulating the level or activity of a polypeptide involved in the synthesis or degradation of sphingosine-1-phosphate (S1P) in a cell, tissue, or subject. The methods involve administration of one or more compounds which modulate the level of gene expression, where the gene encodes a polypeptide involved in regulating the metabolic level of S1P, or modulate the level or activity of a polypeptide involved in regulating the metabolic level of S1P, such as sphingosine kinase (SK) and S1P lyase (SPL). Exemplary methods are directed towards reducing the level of SW by reducing the level or activity of one or more SKs, increasing the level or activity of one or more SPLs, or a combination of both steps.

First claim

What is claimed is:

1. A method of inhibiting the production of a negative-strand RNA virus in a eukaryotic cell, comprising administering a composition comprising one or more agents which modulate the level or activity of a polypeptide involved in the synthesis or degradation of sphingosine-1-phosphate in said cell, wherein said negative-strand RNA virus is in a family selected from the group consisting of Orthomyxoviridae, Paramyxoviridae, Rhabdoviridae, Filoviridae, Bornaviridae, and Bunyaviridae.

2. The method of claim 1 , wherein at least one agent of said composition modulates the activity of a polypeptide which catalyzes the phosphorylation of sphingosine to produce sphingosine-1-phosphate.

3. The method of claim 2 , wherein said polypeptide is sphingosine kinase.

4. The method of claim 3 , wherein the sphingosine kinase is selected from the group consisting of sphingosine kinase 1 and sphingosine kinase 2.

5. The method of claim 2 , wherein at least one of said agents decreases the activity of a sphingosine kinase.

6. The method of claim 5 , wherein the sphingosine kinase is selected from the group consisting of sphingosine kinase 1 and sphingosine kinase 2.

7. The method of claim 5 , wherein said agent is the compound SKI-II (4-[4-(4-Chloro-phenyl)-thiazol-2-ylamino]-phenol); and derivatives of this compound, including acids, salts, enantiomers, mixtures of enantiomers, racemates, esters, amides, prodrugs, and active metabolites, thereof.

8. The method of claim 1 , wherein at least one agent of said composition modulates the activity of a polypeptide which catalyzes the conversion of sphingosine-1-phosphate to phosphoethanolamine and hexadecanal.

9. The method of claim 8 , wherein at least one of said agents increases the activity of said polypeptide.

10. The method of claim 8 , wherein said polypeptide is sphingosine-1-phosphate lyase.

11. A composition for inhibiting the production of a negative-strand RNA virus in a eukaryotic cell, comprising an effective amount of an S1P-modulating agent, wherein the S1P-modulating agent decreases the level of S1P within said cell in a sample of cells contacted with the S1P-modulating agent compared to control sample of cells not contacted with the S1P-modulating agent, wherein said negative-strand RNA virus is in a family selected from the group consisting of Orthomyxoviridae, Paramyxoviridae, Rhabdoviridae, Filoviridae, Bornaviridae, and Bunyaviridae.

12. The composition of claim 11 , wherein at least one of said agents modulates the activity of a polypeptide which catalyzes the phosphorylation of sphingosine to produce sphingosine-1-phosphate.

13. The composition of claim 12 , wherein said polypeptide is sphingosine kinase.

14. The composition of claim 13 , wherein the sphingosine kinase is selected from the group consisting of sphingosine kinase 1 and sphingosine kinase 2.

15. The composition of claim 12 , wherein at least one of said agents decreases the activity of a sphingosine kinase.

16. The composition of claim 15 , wherein the sphingosine kinase is selected from the group consisting of sphingosine kinase 1 and sphingosine kinase 2.

17. The composition of claim 15 , wherein said agent is the compound SKI-II (4-[4-(4-Chloro-phenyl)-thiazol-2-ylamino]-phenol); and derivatives of this compound, including acids, salts, enantiomers, mixtures of enantiomers, racemates, esters, amides, prodrugs, and active metabolites, thereof.

18. The composition of claim 11 , wherein at least one of said agents modulates the activity of a polypeptide which catalyzes the conversion of sphingosine-1-phosphate to phosphoethanolamine and hexadecanal.

19. The composition of claim 18 , wherein at least one of said agents increases the activity of said polypeptide.

20. The composition of claim 18 , wherein said polypeptide is sphingosine-1-phosphate lyase.

21. A method for treating, preventing, or ameliorating one or more symptoms associated with a negative-strand RNA virus infection in a subject, said method comprising administering to said subject in need thereof, a prophylactically- or therapeutically-effective amount of a composition comprising one or more agents which modulate the level or activity of a polypeptide involved in the synthesis or degradation of sphingosine-1-phosphate in said subject, wherein said negative-strand RNA virus is in a family selected from the group consisting of Orthomyxoviridae, Paramyxoviridae, Rhabdoviridae, Filoviridae, Bornaviridae, and Bunyaviridae.

22. The method of claim 21 , wherein at least one agent of said composition modulates the activity of a polypeptide which catalyzes the phosphorylation of sphingosine to produce sphingosine-1-phosphate.

23. The method of claim 22 , wherein said polypeptide is sphingosine kinase.

24. The method of claim 23 , wherein the sphingosine kinase is selected from the group consisting of sphingosine kinase 1 and sphingosine kinase 2.

25. The method of claim 22 , wherein at least one of said agents decreases the activity of a sphingosine kinase.

26. The method of claim 25 , wherein the sphingosine kinase is selected from the group consisting of sphingosine kinase 1 and sphingosine kinase 2.

27. The method of claim 25 , wherein said agent is the compound SKI-II (4-[4-(4-Chloro-phenyl)-thiazol-2-ylamino]-phenol); and derivatives of this compound, including acids, salts, enantiomers, mixtures of enantiomers, racemates, esters, amides, prodrugs, and active metabolites, thereof.

28. The method of claim 21 , wherein at least one agent of said composition modulates the activity of a polypeptide which catalyzes the conversion of sphingosine-1-phosphate to phosphoethanolamine and hexadecanal.

29. The method of claim 28 , wherein at least one of said agents increases the activity of said polypeptide.

30. The method of claim 28 , wherein said polypeptide is sphingosine-1-phosphate lyase.

Assignees

• Hahm Bumsuk
• Seo Young-Jin
• Alexander Stephen
• Madhuvanthi Vijayan
• Univ Missouri

Inventors

• Hahm Bumsuk
• Seo Young-Jin
• Alexander Stephen
• Madhuvanthi Vijayan

Classifications

• A61K48/005

  characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered · CPC title

• C12N15/113

  Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; {Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing (when used in plants C12N15/8218)} · CPC title

• C12Y401/02027

  Sphinganine-1-phosphate aldolase (4.1.2.27) · CPC title

• C12N15/1138

  against receptors or cell surface proteins · CPC title

• A61P31/00

  Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title