Pharmaceutical compositions having antibacterial, antiviral, and other immunostimulatory activities
The present disclosure relates to pharmaceutical compositions including an active substance with antimicrobial, antiviral, and immunoistimulatory activities. The disclosure further provides methods of treating bacterial or viral infections and methods of enhancing immune function using the active substance.
1. A method of treating a bacterial infection or a viral infection in a subject in need thereof comprising administering to the subject an effective amount of a pharmaceutical composition comprising an active substance and a pharmaceutically acceptable carrier or filler, wherein the active substance comprises:
(i) 40-60% (w/w) polysaccharide, wherein the polysaccharide comprises the following structure:
wherein m=3-5 and every second α-L-Rhap residue bears an R substituent,
R is a monosaccharide or an oligosaccharide comprising β-D-galactopyranose and optionally comprising α-L-arabinofuranose,
and the polysaccharide portion comprises a weight ratio of rhamnose to galacturonic acid of 1:6 to 1:4;
(ii) 4-20% (w/w) peptide; and
(iii) 2-7% (w/w) lipid.
2. The method of claim 1 , wherein the method is for treating a bacterial infection.
3. The method of claim 1 , wherein the method is for treating a viral infection.
4. The method of claim 1 , wherein the active substance has immunostimulatory activity.
5. The method of claim 4 , wherein the active substance activates dendritic cells.
6. The method of claim 4 , wherein the active substance activates macrophages.
7. The method of claim 1 , wherein the active substance increases the production of cytokines in the subject.
8. The method of claim 1 , wherein the bacterial or viral infection is a bacterial or viral infection of a wound.
9. The method of claim 8 , wherein administering the active substance to the subject decreases local edema around the wound, decreases local hyperemia around the wound, or decreases the healing time of the wound, as compared to a subject not having been administered the active substance.
10. The method of claim 1 , wherein the molecular weight of the active substance is 500 kDa to 17,000 kDa.
11. The method of claim 1 , wherein the polysaccharide does not comprise glucose.
12. The method of claim 1 , wherein R is an oligosaccharide comprising β-D-galactopyranose and α-L-arabinofuranose.
13. A method of enhancing the immune function of a cell comprising contacting the cell with an effective amount of a pharmaceutical composition comprising an active substance and a pharmaceutically acceptable carrier or filler, wherein the active substance comprises:
(i) 40-60% (w/w) polysaccharide, wherein the polysaccharide comprises the following structure:
wherein m=3-5 and every second α-L-Rhap residue bears an R substituent,
R is a monosaccharide or an oligosaccharide comprising β-D-galactopyranose and optionally comprising α-L-arabinofuranose,
and the polysaccharide portion comprises a weight ratio of rhamnose to galacturonic acid of 1:6 to 1:4;
(ii) 4-20% (w/w) peptide; and
(iii) 2-7% (w/w) lipid.
14. The method of claim 13 , wherein the cell is a dendritic cell.
15. The method of claim 13 , wherein the cell is a macrophage.
16. The method of claim 13 , wherein the active substance increases the production of cytokines in the cell.
17. The method of claim 13 , wherein the cell is in a subject in need of enhanced immune function, and the active substance is administered to the subject thereby enhancing the immune function of the subject.
18. The method of claim 13 , wherein the molecular weight of the active substance is 500 kDa to 17,000 kDa.
19. The method of claim 13 , wherein the polysaccharide does not comprise glucose.
20. The method of claim 13 , wherein R is an oligosaccharide comprising β-D-galactopyranose and α-L-arabinofuranose.