US2022169976A1PendingUtilityA1
Probiotic bifidobacterium strain
Est. expiryNov 11, 2029(~3.3 yrs left)· nominal 20-yr term from priority
A61P 17/06A61P 1/16A61P 25/28A61P 31/10C12R 2001/01A61P 11/00A61P 7/02A23C 9/1234A61P 29/00A61P 7/06A61K 35/745A61P 31/00A23G 9/363A61P 1/02A61P 37/08A61P 3/00A61P 9/00A61P 3/04A61P 1/00A61P 37/06A61P 31/18A61P 1/12A61P 17/02A23L 33/135A61P 9/10A23V 2002/00A61P 15/00C12N 1/205A61P 19/02A61P 37/02Y02A50/30A61P 31/12A61P 5/00C12N 1/20A61P 37/00A61P 11/06A61P 19/10A61P 13/12A61P 31/04A61P 17/00A61P 17/10A61P 1/04A61P 35/04A61P 3/10A61P 25/00A61P 35/00A23Y 2300/55A23V 2400/533
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Claims
Abstract
Probiotic Bifidobacterium strain AH1714 is significantly immunomodulatory following oral consumption. The strain is useful as an immunomodulatory biotherapeutic agent.
Claims
exact text as granted — not AI-modified1 - 38 . (canceled)
39 . A method for preventing inflammation in the gastrointestinal system of a subject, the method comprising administering to the subject an oral formulation comprising isolated strain Bifidobacterium longum deposited with NCIMB under accession number NCIMB 41676, wherein the Bifidobacterium longum strain is in the form of a powder.
40 . The method of claim 39 , wherein the formulation modulates cytokine levels in the subject, such that the subject has increased production of anti-inflammatory cytokines.
41 . The method of claim 39 , wherein the subject has increased production of IL-10.
42 . The method of claim 39 , wherein the formulation inhibits production of TNF-α in the subject.
43 . The method of claim 39 , wherein the formulation inhibits production of IFN-γ in the subject.
44 . The method of claim 39 , wherein the formulation inhibits production of IL-12 in the subject.
45 . The method of claim 39 , wherein the subject is a human.
46 . The method of claim 39 , wherein the formulation comprises an ingestible carrier.
47 . The method of claim 46 , wherein the ingestible carrier comprises a dairy product.
48 . The method of claim 46 , wherein the ingestible carrier comprises a dressing or a beverage.
49 . The method of claim 39 , wherein the formulation comprises more than 10 6 cfu of the Bifidobacterium longum strain per gram of the formulation.
50 . A method for preventing inflammation in the gastrointestinal system of a subject, the method comprising administering to the subject an oral formulation comprising isolated strain Bifidobacterium longum deposited with NCIMB under accession number NCIMB 41676 and an ingestible carrier, wherein the subject is a human.
51 . The method of claim 50 , wherein the formulation modulates cytokine levels in the subject, such that the subject has increased production of IL-10.
52 . The method of claim 50 , wherein the formulation inhibits production of TNF-α, IFN-γ, or both in the subject.
53 . The method of claim 50 , wherein the formulation comprises more than 10 6 cfu of the Bifidobacterium longum strain per gram of the formulation.
54 . The method of claim 50 , wherein the formulation is administered in the form of a food product or a beverage.
55 . The method of claim 50 , wherein the formulation is administered in the form of a capsule or a tablet.
56 . A method for preventing inflammation in the gastrointestinal system of a subject, the method comprising administering to the subject an oral formulation comprising isolated strain Bifidobacterium longum deposited with NCIMB under accession number NCIMB 41676 and an ingestible carrier, wherein the formulation comprises more than 10 6 cfu per gram of the Bifidobacterium longum strain.
57 . The method of claim 56 , wherein the formulation is administered in the form of a food product or a beverage.
58 . The method of claim 56 , wherein the formulation modulates cytokine levels in the subject, such that the subject has increased production of IL-10 and reduced production of TNF-α, IFN-γ, or both.Cited by (0)
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