Polypeptide and immune modulation
US-9796762-B2 · Oct 24, 2017 · US
US11058732B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11058732-B2 |
| Application number | US-201916703980-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 5, 2019 |
| Priority date | Nov 20, 2015 |
| Publication date | Jul 13, 2021 |
| Grant date | Jul 13, 2021 |
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The invention provides compositions comprising bacterial strains for treating and preventing cancer.
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What is claimed is: 1. A method of increasing a level of an IL-6 or TNF-α cytokine in a subject in need thereof, comprising administering to said subject a pharmaceutical composition that comprises: (a) a bacteria strain of the species Enterococcus gallinarum that comprises a 16s rRNA gene sequence with at least 99.5% sequence identity to the polynucleotide of SEQ ID NO: 2, wherein said sequence identity is determined by the Smith-Waterman homology search algorithm using an affine gap search with a gap open penalty of 12 and a gap extension penalty of 2, and a BLOSUM matrix of 62, and (b) a prebiotic compound, wherein said administering is sufficient to increase said level of said IL-6 or TNF-α cytokine at least 100-fold relative to prior to said administering. 2. The method of claim 1 , wherein said administering is sufficient to increase said level of said IL-6 cytokine. 3. The method of claim 2 , wherein said administering is sufficient to increase said level of said IL-6 cytokine at least 600-fold, relative to prior to said administering. 4. The method of claim 1 , wherein said administering is sufficient to increase said level of said TNF-α cytokine. 5. The method of claim 4 , wherein said administering is sufficient to increase said level of said IL-6 cytokine at least 400-fold, relative to prior to said administering. 6. The method of claim 1 , wherein said pharmaceutical composition further comprises a lipopolysaccharide. 7. The method of claim 6 , wherein said administering is sufficient to increase a level of an IL-1β cytokine at least 1000-fold, relative to prior to said administering. 8. The method of claim 1 , wherein said amount of said bacteria strain comprises from about 1×10 3 to about 1×10 11 CFU/g of said bacteria strain with respect to a total weight of said pharmaceutical composition. 9. The method of claim 1 , wherein said pharmaceutical composition is formulated for oral delivery. 10. The method of claim 1 , wherein said pharmaceutical composition is formulated for delivery to an intestine of said subject. 11. The method of claim 1 , wherein said subject is human. 12. The method of claim 1 , wherein said prebiotic compound is 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.
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