US2021069258A1PendingUtilityA1

Compositions comprising bacterial strains

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Assignee: 4D PHARMA RES LTDPriority: Nov 23, 2015Filed: Jun 23, 2020Published: Mar 11, 2021
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-modified
1 .- 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.

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