IP Library Granted Patent US 11,723,933
Granted Patent B2
US 11,723,933 · App. 16/247,834 · Granted Aug 15, 2023

Composition of bacteroides thetaiotaomicron for immune modulation

Inventors: Angela Margaret Patterson (Norwich, GB); George Grant (Aberdeen, GB); Imke Mulder (Aberdeen, GB)
Assignee: CJ BIOSCIENCE, INC.
A61K35/74A23L33/135A61K9/0053A61K9/19C12N1/04C12N1/205A23V2002/00C12R2001/01
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Quick Facts
Patent No.
US 11,723,933
App. No.
16/247,834
Granted
Aug 15, 2023
Kind
B2
Abstract

The present invention provides a strain of Bacteroides thetaiotaomicron and derivatives thereof, and the use of said strain or derivatives in treating inflammatory, autoimmune and allergic disorders. The invention also provides pharmaceutical compositions, nutritional supplements, feedstuffs, food products, dietary supplements, and food additives comprising said strain or derivatives.

Claims (23)

1. A method of treating an inflammatory disorder in a subject in need thereof comprising administering to said subject a pharmaceutical composition that comprises an amount of a Bacteroides thetaiotaomicron bacteria strain deposited under accession number NCIMB 42341.

2. The method of claim 1 , wherein said administering of said pharmaceutical composition reduces inflammation in a tissue or organ.

3. The method of claim 1 , wherein said inflammatory disorder affects a section of an alimentary canal or an epithelial cell; and wherein said administering reduces inflammation of said section of said alimentary canal or said epithelial cell.

4. The method of claim 1 , wherein said inflammatory disorder is selected from the group consisting of inflammatory bowel disorder (IBD), colitis, rheumatoid arthritis, psoriasis, multiple sclerosis, type I diabetes, celiac disease, atopic dermatitis, rhinitis, irritable bowel syndrome (IBS), ulcerative colitis, pouchitis, Crohn's disease, functional dyspepsia, atopic diseases, necrotizing enterocolitis, non-alcoholic fatty liver disease, gastrointestinal infection, and any combination thereof.

5. The method of claim 1 , wherein said administering of said pharmaceutical composition reduces disruption to a colon of said subject.

6. The method of claim 1 , wherein said administering of said pharmaceutical composition:

a. reduces or prevents disruption to an integrity of a mucosal epithelium;

b. reduces or prevents a reduction in a number of goblet cells in the epithelium;

c. reduces or prevents infiltration of immune cells into a lamina propria; or

d. any combination thereof.

7. The method of claim 1 ; wherein said administering of said pharmaceutical composition is sufficient to reduce an expression of at least one pro-inflammatory gene in said subject relative to an amount prior to said administering.

8. The method of claim 7 , wherein said at least one pro-inflammatory gene is selected from the group consisting of IL1-β, IL4, IL5, IL6, IL8, IL12, IL13, IL17, IL21, IL22, IL23, IL27, IFN, CCL2, CCL3, CCL5, CCL20, CXCL5, CXCL10, CXCL12, CXCL13, TNF-α, and any combination thereof.

9. The method of claim 1 , wherein said administering of said pharmaceutical composition is sufficient to increase an expression of at least one pro-barrier integrity gene in said subject relative to an amount prior to said administering.

10. The method of claim 9 , wherein said pro-barrier integrity gene is selected from the group consisting of Retnlg, Retnlb, Si, Defa24, Hsd11b2, Hsd17b2, and Nr1d1.

11. The method of claim 1 , wherein said administering of said pharmaceutical composition is sufficient to increase an amount of regulatory T cells in a section of an alimentary canal relative to an amount prior to said administering.

12. The method of claim 1 , wherein said pharmaceutical composition is encapsulated.

13. The method of claim 1 , wherein said pharmaceutical composition is formulated for oral delivery.

14. The method of claim 13 , wherein said pharmaceutical composition comprises an enteric coating.

15. The method of claim 1 , wherein said amount comprises from about 1×10 3 to about 1×10 12 CFU/g of said Bacteroides thetaiotaomicron bacteria strain with respect to a total weight of said pharmaceutical composition.

16. The method of claim 1 , wherein said Bacteroides thetaiotaomicron bacteria strain is live and viable.

17. The method of claim 1 , further comprising an additional bacteria strain.

18. The method of claim 17 , wherein said additional bacteria strain is Roseburia hominis.

19. A method of treating a disorder in a subject in need thereof comprising administering to said subject a pharmaceutical composition that comprises an amount of a Bacteroides thetaiotaomicron bacteria strain, wherein said disorder is selected from the group consisting of type I diabetes, celiac disease, atopic dermatitis, rhinitis, pouchitis, functional dyspepsia, atopic diseases, necrotizing enterocolitis, non-alcoholic fatty liver disease, gastrointestinal infection, and any combination thereof.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2023
From: 4D PHARMA PLC; 4D PHARMA RESEARCH LIMITED
To: CJ BIOSCIENCE, INC.
Reel/Frame 063992/0427 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2022
From: OXFORD FINANCE LUXEMBOURG S.A R.L.
To: ARMISTICE CAPITAL MASTER FUND LTD.
Reel/Frame 061806/0371 →
INTELECTUAL PROPERTY SECURITY AGREEMENT Recorded Jul 30, 2021
From: 4D PHARMA PLC; 4D PHARMA RESEARCH LIMITED; 4D PHARMA CORK LIMITED; 4D PHARMA DELAWARE INC.
To: OXFORD FINANCE LUXEMBOURG S.A R.L.
Reel/Frame 057042/0715 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2020
From: PATTERSON, ANGELA MARGARET; GRANT, GEORGE; MULDER, IMKE
To: 4D PHARMA RESEARCH LIMITED
Reel/Frame 051554/0924 →
Priority Claims (1)
GB 1423084 · Dec 23, 2014 · national
Continuity (3)
Division 15631945 · Jun 23, 2017
Continuation PCTGB2015054112 · Dec 22, 2015
Related Publication 20190134108A1 · May 9, 2019