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Broad antiviral therapy with membrane modifying oxysterols

a technology of oxysterols and broad antiviral therapy, which is applied in the direction of macromolecular non-active ingredients, biochemistry apparatus and processes, drug compositions, etc., can solve the problem that their roles in the immune system remain elusiv

Inactive Publication Date: 2015-05-14
RGT UNIV OF CALIFORNIA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent text describes the discovery of a new gene called Ch25h, which is induced by interferons and is involved in the immune response to viruses. The patent aims to protect the use of this gene and its related proteins for the development of new antiviral therapies that can work against a broad range of viruses. The technical effect of this patent is the discovery and validation of a new gene and its related proteins that can be used to develop new antiviral therapies.

Problems solved by technology

Although these studies support a conserved immunological role of Ch25h and 25HC, their roles in the immune system remain elusive.

Method used

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  • Broad antiviral therapy with membrane modifying oxysterols
  • Broad antiviral therapy with membrane modifying oxysterols
  • Broad antiviral therapy with membrane modifying oxysterols

Examples

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example 1

References for Example 1

[0166]Andrew J, and Jessup, W. (1999). Oxysterols and atherosclerosis. Atherosclerosis 142, 1-28.[0167]Bauman, D. R., Bitmansour, A. D., McDonald, J. G., Thompson, B. M., Liang, G., and Russell,[0168]D. W. (2009). 25-Hydroxycholesterol secreted by macrophages in response to Toll-like receptor activation suppresses immunoglobulin A production. Proceedings of the National Academy of Sciences 106, 16764-16769.[0169]Brass, A. L., Huang, I.-C., Benita, Y., John, S. P., Krishnan, M. N., Feeley, E. M., Ryan, B. J., Weyer, J. L., van der Weyden, L., Fikrig, E., et al. (2009). The IFITM Proteins Mediate Cellular Resistance to Influenza A H1N1 Virus, West Nile Virus, and Dengue Virus. Cell 139, 1243-1254.[0170]Butler, S. L., Hansen, M. S. T., and Bushman, F. D. (2001). A quantitative assay for HIV DNA integration in vivo. Nat Med 7,631-634.[0171]Cavrois, M., de Noronha, C., and Greene, W. C. (2002). A sensitive and specific enzyme-based assay detecting HIV-1 virion fus...

example 2

References for Example 2

[0219]Butler, S. L., Hansen, M. S. T., and Bushman, F. D. (2001). A quantitative assay for HIV DNA integration in vivo. Nat Med 7, 631-634.[0220]Cavrois, M., de Noronha, C., and Greene, W. C. (2002). A sensitive and specific enzyme-based assay detecting HIV-1 virion fusion in primary T lymphocytes. Nat Biotech 20, 1151-1154.[0221]Korin, Y. D., and Zack, J. A. (1999). Nonproductive Human Immunodeficiency Virus Type 1 Infection in Nucleoside-Treated G0 Lymphocytes. Journal of Virology 73, 6526-6532.[0222]Liu, X. V., Ho, S. S. W., Tan, J. J., Kamran, N., and Gasser, S. (2012). Ras Activation Induces Expression of Raet1 Family NK Receptor Ligands. The Journal of Immunology 189, 1826-1834.[0223]Miller, B. T., Ueta, C. B., Lau, V., Jacomino, K. G., Wasserman, L. M., and Kim, B. W. (2012). Statins and Downstream Inhibitors of the Isoprenylation Pathway Increase Type 2 Iodothyronine Deiodinase Activity. Endocrinology 153, 4039-4048.[0224]Mortazavi, A., Williams, B. A...

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Abstract

This invention relates, e.g., to a method for inhibiting the growth and / or proliferation and / or infectivity of a virus in a cell, such as a mammalian cell (e.g. for inhibiting entry of the virus into the cell), comprising administering, or causing to be administered, to the cell, 25-hydroxycholesterol (25HC) in an amount sufficient to inhibit the growth and / or proliferation and / or infectivity of the virus in the cell. The method can be carried out in vivo or in vitro. Among the viruses that can be inhibited are, e.g., VSV, HSV, MHV68, HCV, HIV, EBOV, RVFV, RSSEV and Nipah virus. In one embodiment of the invention, the 25HC is administered topically, e.g. to a mucosal surface.

Description

[0001]This application claims the benefit of the filing date of U.S. Provisional application 61 / 643,110, filed May 4, 2012, which is incorporated by reference herein in its entirely.SEQUENCE LISTING[0002]The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on May 3, 2013, is named 58086-347965_SL.txt and is 3,313 bytes in size.BACKGROUND INFORMATION[0003]Viruses are obligate intracellular pathogens that—despite having unique structure and function—undergo lifecycle stages of entry, replication, protein synthesis, assembly, and egress. Upon specific binding to cell surface molecules, non-enveloped virus can enter the cell directly while enveloped viruses undergo fusion process that requires specific interactions between the viral and cellular receptors and membranes. After entry, viral components are released into the cytoplasm and may enter the nucleu...

Claims

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Application Information

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IPC IPC(8): A61K31/575
CPCA61K31/575A61K47/40A61P31/00A61P31/12
Inventor CHENG, GENHONGLIU, SU-YANG
Owner RGT UNIV OF CALIFORNIA
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