US2021069258A1PendingUtilityA1
Compositions comprising bacterial strains
Est. expiryNov 23, 2035(~9.4 yrs left)· nominal 20-yr term from priority
Y02A50/30C12N 1/205C12R 2001/145A61P 37/02A61K 31/00A61K 35/74A61K 9/19A61P 35/04A61P 11/08A61K 39/08A61P 11/00A61P 9/00A61K 2039/542A61P 25/00A61P 17/02A61K 2035/11A61P 17/00A61P 19/00A23L 33/135A61P 37/06A61P 29/00A61K 2039/577A61P 17/04A61P 27/02A61P 37/00A23V 2002/00A61P 9/10A61P 17/06A61P 7/00A61K 2039/55594A61P 1/04A61P 35/00A61K 2039/58A61P 37/08A61K 39/39A61K 2300/00A61P 19/08A61P 19/02A61P 25/28A61P 1/02A61P 1/00A61P 11/02A61P 11/06A61P 43/00A23C 9/152
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Claims
Abstract
The invention provides compositions comprising bacterial strains for treating and preventing inflammatory and autoimmune diseases.
Claims
exact text as granted — not AI-modified1 .- 30 . (canceled)
31 . A method of treating a subject in need thereof, comprising:
administering to said subject a pharmaceutical composition that comprises at least 1×10 3 colony forming units (CFU)/g of a bacteria strain of the genus Erysipelatoclostridium with respect to a total weight of said pharmaceutical composition, wherein said bacteria strain comprises a polynucleotide of a 16S rRNA gene that has at least 95% identity to the polynucleotide sequence of SEQ ID NO:3, as determined by a Smith-Waterman homology search algorithm using an affine gap search with a gap open penalty of 12, a gap extension penalty of 2, and a BLOSUM of 62, and wherein said pharmaceutical composition comprises said bacteria strain in a therapeutically effective amount that is sufficient to treat said subject when administered to said subject.
32 . The method of claim 31 , wherein said bacteria strain is capable of at least partially colonizing an intestine of said subject.
33 . The method of claim 31 , wherein said pharmaceutical composition is formulated for delivery to an intestine of said subject.
34 . The method of claim 31 , wherein said pharmaceutical composition is encapsulated.
35 . The method of claim 31 , wherein said bacterial strain is dried.
36 . The method of claim 31 , wherein said administering comprises oral, rectal, nasal, buccal, sublingual, or subcutaneous administration.
37 . The method of claim 31 , wherein said pharmaceutical composition further comprises a pharmaceutically acceptable excipient, diluent, or carrier.
38 . The method of claim 31 , wherein said pharmaceutical composition comprises from about 1×10 3 to about 1×10 11 CFU/g of the bacteria strain with respect to the total weight of said pharmaceutical composition.
39 . The method of claim 31 , wherein said bacteria strain comprises a polynucleotide of a 16S rRNA gene that has at least 99% identity to the polynucleotide sequence of SEQ ID NO:3, as determined by a Smith-Waterman homology search algorithm using an affine gap search with a gap open penalty of 12, a gap extension penalty of 2, and a BLOSUM of 62.
40 . The method of claim 31 , wherein said bacteria strain comprises a 16S rRNA gene that comprises the polynucleotide sequence of SEQ ID NO: 3.
41 . The method of claim 31 , wherein said bacteria strain is the strain deposited with the NCIMB accession number NCIMB 42688.
42 . The method of claim 31 , wherein said bacteria strain is of species Erysipelatoclostridium ramosum.
43 . The method of claim 31 , wherein said bacteria strain is a spore-forming bacterial strain.
44 . The method of claim 31 , wherein said subject is human.Cited by (0)
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