Porcine lactic acid bacterial strains
US-9539293-B2 · Jan 10, 2017 · US
US9839655B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9839655-B2 |
| Application number | US-201615357850-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 21, 2016 |
| Priority date | Nov 20, 2015 |
| Publication date | Dec 12, 2017 |
| Grant date | Dec 12, 2017 |
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The invention provides compositions comprising bacterial strains for treating and preventing cancer.
Opening claim text (preview).
What is claimed is: 1. A pharmaceutical composition that comprises: a therapeutically effective amount of a bacteria strain of the species Enterococcus gallinarum deposited under accession number NCIMB 42488; and a pharmaceutically acceptable excipient, diluent, or carrier; wherein said therapeutically effective amount of said bacteria strain is an amount sufficient for treating cancer in a subject, and wherein said bacteria strain is lyophilized. 2. The pharmaceutical composition of claim 1 , wherein said pharmaceutically acceptable excipient, diluent, or carrier further comprises a lyoprotectant. 3. The pharmaceutical composition of claim 1 , wherein said pharmaceutical composition further comprises at least one additional bacteria strain. 4. The pharmaceutical composition of claim 1 , wherein at least 50% of said bacteria strain, as measured by an amount of colony forming units (CFU), remains viable after about 1 year of storage when said pharmaceutical composition is stored in a closed container at 25° C. at 95% relative humidity. 5. The pharmaceutical composition of claim 1 , wherein said therapeutically effective amount of said bacteria strain comprises from about 1×10 6 to about 1×10 11 CFU/g of said bacteria strain with respect to a total weight of said pharmaceutical composition. 6. The pharmaceutical composition of claim 1 , wherein said pharmaceutical composition further comprises a lipopolysaccharide. 7. The pharmaceutical composition of claim 1 , wherein said therapeutically effective amount is an amount effective to increase production of at least one cytokine selected from the group consisting of IL-6, TNF-α, and IL-1β. 8. The pharmaceutical composition of claim 1 , wherein said pharmaceutical composition is formulated for oral delivery. 9. The pharmaceutical composition of claim 1 , wherein said pharmaceutical composition further comprises a prebiotic compound selected from the group consisting of: a fructo-oligosaccharide, a short-chain fructo-oligosaccharide, inulin, an isomalt-oligosaccharide, a transgalacto-oligosaccharide, a pectin, a xylo-oligosaccharide, a chitosan-oligosaccharide, a beta-glucan, an arable gum modified starch, a polydextrose, a D-tagatose, an acacia fiber, carob, an oat, and a citrus fiber. 10. The pharmaceutical composition of claim 1 , wherein said pharmaceutical composition further comprises an adjuvant.
lyophilised {, i.e. freeze-dried, solutions or dispersions (lyophilised products with subsequent particle size reduction A61K9/14; granules or pellets made by lyphilisation A61K9/1682; solid oral dosage forms made by lyophilisation A61K9/2095; lyophilisation additives A61K47/00)} · CPC title
Antineoplastic agents · CPC title
{Lactobacillales, e.g. aerococcus, enterococcus, lactobacillus, lactococcus}, streptococcus · CPC title
Lipopolysaccharides · CPC title
Immunostimulants · CPC title
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