US2022016184A1PendingUtilityA1
Compositions comprising bacterial strains
Est. expiryMay 22, 2037(~10.9 yrs left)· nominal 20-yr term from priority
A61K 35/74A61K 9/0031A61P 25/00A61P 25/24A61K 35/741A23L 33/135A61P 25/16A61K 9/0053A61P 25/22C12N 1/20A61K 9/48A61P 25/18A61P 25/28
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Claims
Abstract
The invention provides compositions comprising bacterial strains for treating and preventing brain injury.
Claims
exact text as granted — not AI-modified1 .- 31 . (canceled)
32 . A method of treating a brain injury in a subject in need thereof, comprising administering to the subject a composition that comprises a therapeutically effective amount of a bacteria strain of the genus Blautia , wherein the bacteria strain comprises a 16S rRNA gene sequence having at least 95% sequence identity to the polynucleotide sequence of SEQ ID NO:5, and wherein the administering is effective to treat the brain injury.
33 . The method of claim 32 , wherein the administering is effective to improve a loss of neurological function, motor abilities and/or social recognition associated with the brain injury.
34 . The method of claim 32 , wherein the brain injury is resulting from a trauma, a tumor, a brain hemorrhage, an encephalitis, a cerebral hypoxia, or a cerebral anoxia.
35 . The method of claim 34 , wherein the brain hemorrhage is an intracerebral hemorrhage, an intraparenchymal hemorrhage, an intraventricular hemorrhage, or a subarachnoid hemorrhage.
36 . The method of claim 32 , wherein the brain injury is caused by a cerebral amyloid angiopathy, a brain aneurysm, or a cerebral arteriovenous malformation (AVM).
37 . The method of claim 32 , wherein the therapeutically effective amount comprises from about 1×10 3 to about 1×10 11 colony forming units (CFU).
38 . The method of claim 32 , wherein the composition comprises the bacterial strain in an amount of from about 1×10 6 to about 1×10 11 colony forming units per gram (CFU/g), with respect to the weight of the composition.
39 . The method of claim 32 , wherein the composition comprises no more than de minimis amounts of other bacteria strains.
40 . The method of claim 32 , wherein the bacteria strain is live.
41 . The method of claim 32 , wherein the bacteria strain is capable of at least partially colonizing an intestine of the subject.
42 . The method of claim 32 , wherein the administering comprises oral, rectal, nasal, buccal, sublingual, or subcutaneous administration.
43 . The method of claim 32 , wherein the composition is formulated for delivery to an intestine of the subject.
44 . The method of claim 32 , wherein the composition is encapsulated.
45 . The method of claim 32 , wherein the bacteria strain is lyophilized.
46 . The method of claim 32 , wherein the bacteria strain is of the species Blautia hydrogenotrophica.
47 . The method of claim 32 , wherein the bacteria strain comprises a 16S rRNA gene sequence having at least 98% sequence identity to the polynucleotide sequence of SEQ ID NO:5
48 . The method of claim 32 , wherein the bacteria strain comprises a 16S rRNA gene sequence that is the polynucleotide sequence of SEQ ID NO:5.
49 . The method of claim 32 , wherein the bacteria strain is the strain deposited under accession number DSM 14294 or a biotype of the strain deposited under accession number DSM 14294.
50 . The method of claim 49 , wherein the biotype is a bacteria strain that has the same carbohydrate fermentation pattern as the bacteria strain deposited under accession number DSM 14294.
51 . The method of claim 32 , wherein the composition further comprises a pharmaceutically acceptable excipient or carrier.Cited by (0)
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