Compounds, compositions, and methods for the treatment of inflammatory, degenerative, and neurodegenerative diseases
US-2024409487-A1 · Dec 12, 2024 · US
US11278556B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11278556-B2 |
| Application number | US-201816488865-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 27, 2018 |
| Priority date | Feb 27, 2017 |
| Publication date | Mar 22, 2022 |
| Grant date | Mar 22, 2022 |
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The invention generally relates to methods to prevent and/or inhibit viral infection as well as to inhibit inflammation and/or pathogen infection by administering at least one xylitol lipid analog or compositions comprising at least one xylitol lipid analog to an individual. The invention also relates to methods to prevent or inhibit respiratory syncytial virus (RSV) infection by administering at least one xylitol lipid analog or compositions comprising at least one xylitol lipid analog to an individual.
Opening claim text (preview).
What is claimed: 1. A method to inhibit respiratory syncytial virus (RSV) infection in an individual who has, or is at risk of developing, RSV infection, the method comprising administering to the individual at least one xylitol lipid analog, wherein an amount of the xylitol lipid analog is effective to inhibit said viral infection, and wherein the xylitol lipid analog is Diether-phosphatidylxylitol (DEPX) or an analog thereof. 2. The method of claim 1 , wherein the RSV infection activates at least one Toll-like receptor (TLR) selected from the group consisting of TLR1, TLR2, TLR3, TLR4, TLR6, TLR7, TLR8, TLR9, and TLR10. 3. The method of claim 1 , wherein the DEPX lipid analog is selected from the group consisting of 14:0 Diether-phosphatidylxylitol (14:0 DEPX) and 18:1 Diether-phosphatidylxylitol (18:1 DEPX). 4. The method of claim 1 , wherein the individual is a neonatal infant. 5. The method of claim 1 , wherein the xylitol lipid analog is administered to the individual prior to any indication of viral infection. 6. The method of claim 1 , wherein the xylitol lipid analog is administered to the individual subsequent to identification of a symptom of, or confirmation of, viral infection of the individual. 7. The method of claim 1 , wherein the xylitol lipid analog is administered as a homogeneous lipid preparation. 8. The method of claim 1 , wherein the xylitol lipid analog is administered as a composition comprising a homogeneous lipid preparation of the xylitol lipid analog. 9. The method of claim 1 , wherein the xylitol lipid analog is administered as a composition comprising a preparation of randomly mixed surfactant lipids combined with a homogeneous lipid preparation of the xylitol lipid analog. 10. The method of claim 1 , wherein the xylitol lipid analog is administered as a preparation of randomly mixed surfactant lipids, wherein the xylitol lipid analog comprises at least about 50% of the total lipids in said randomly mixed surfactant lipids. 11. The method of claim 1 , wherein the xylitol lipid analog is administered via respiratory tract of the individual. 12. The method of claim 1 , wherein the xylitol lipid analog is administered via nasal passages of the individual. 13. The method of claim 1 , wherein the xylitol lipid analog suppresses activation of at least one TLR selected from the group consisting of TLR1, TLR2, TLR3, TLR4, and TLR7. 14. The method of claim 1 , wherein the xylitol lipid analog is administered in combination with at least one material selected from the group consisting of POPG, SP-A and SP-D.
Adducts, complexes, salts of phosphatides · CPC title
having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate · CPC title
Nose · CPC title
for RNA viruses · CPC title
Antivirals · CPC title
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