IP Library Granted Patent US 8,658,622
Granted Patent B2
US 8,658,622 · App. 11/795,183 · Granted Feb 25, 2014

Methods and compositions for preventing and treating a disease related to glycan dysregulation

Inventors: Michael Demetriou (Irvine, CA); James Dennis (Etobicoke, CA); Ken Siu-Kwong Lau (Toronto, CA)
Assignees: Regents of the University of California; Mount Sinai Hospital
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Quick Facts
Patent No.
US 8,658,622
App. No.
11/795,183
Granted
Feb 25, 2014
Kind
B2
Abstract

Contemplated compositions and methods are directed to prevent and/or treat various autoimmune diseases that are typically associated with glycan dysregulation, and especially autoimmune demyelinating diseases. Further especially contemplated aspects include animal models and systems for screening compounds to treat and/or prevent such diseases.

Claims (25)

1. A method of treating multiple sclerosis comprising:

administering to a subject having multiple sclerosis a therapeutically effective amount of a nutraceutical or pharmaceutical composition comprising a metabolite of a pathway for synthesis of a sugar donor for Mgat5 and a pharmaceutically acceptable or nutraceutically acceptable carrier,

wherein said metabolite is N-acetylglucosamine (GlcNAc) or N-acetylglucosamine-tetra-acetate; and

wherein the level of Mgat5 modified glycans is increased in the subject, thereby treating the subject's multiple sclerosis.

2. The method of claim 1 , further comprising administering a therapeutically effective amount of a nutraceutical or pharmaceutical, composition comprising uridine, uridine 5′ diphosphate (UDP), uridine 5′ monophosphate (UMP), uridine 5′ triphosphate (UTP), uracil, or a nutraceutically acceptable derivative thereof, and a pharmaceutically acceptable or nutraceutically acceptable carrier.

3. The method of claim 2 , further comprising administering a therapeutically effective amount of a nutraceutical or pharmaceutical composition comprising Vitamin D3 and a pharmaceutically acceptable or nutraceutically acceptable carrier.

4. The method of claim 1 , further comprising administering a therapeutically effective amount of a nutraceutical or pharmaceutical composition comprising Vitamin D3 and a pharmaceutically acceptable or nutraceutically acceptable carrier.

5. The method of claim 1 , wherein the nutraceutical or pharmaceutical composition is administered orally.

6. A method for treatment of multiple sclerosis comprising:

administering to a subject having multiple sclerosis a nutraceutical or pharmaceutical composition comprising:

i. N-acetylglucosamine (GlcNAc) or N-acetylglucosamine-tetra-acetate;

ii. uridine, uridine 5′ diphosphate (UDP), uridine 5′ monophosphate (UMP), uridine 5′ triphosphate (UTP), uracil, or a nutraceutically acceptable derivative thereof;

iii. Vitamin D3; and

iv. a pharmaceutically acceptable or nutraceutically acceptable carrier;

wherein the level of Mgat5 modified glycans is increased in the subject, thereby treating the subject's multiple sclerosis.

7. The method of claim 6 , wherein the nutraceutical or pharmaceutical composition is administered orally.

8. A method for treatment of multiple sclerosis comprising administering to a subject having multiple sclerosis a nutraceutical or pharmaceutical composition comprising therapeutically effective amounts of:

i. N-acetylglucosamine (GlcNAc) or N-acetylglucosamine-tetra-acetate; and

ii. uridine, uridine 5′ diphosphate (UDP), uridine 5′ monophosphate (UMP), uridine 5′ triphosphate (UTP), uracil, or a nutraceutically acceptable derivative thereof; and

iii. a pharmaceutically acceptable or nutraceutically acceptable carrier;

wherein the level of Mgat5 modified glycans is increased in the subject, thereby treating the subject's multiple sclerosis.

9. The method of claim 8 , wherein the nutraceutical or pharmaceutical composition is administered orally.

10. The method according to claim 2 , wherein said nutraceutically acceptable derivative is a salt, hydrate or ester.

11. The method according to claim 6 , wherein said nutraceutically acceptable derivative is a salt, hydrate or ester.

12. The method according to claim 8 , wherein said nutraceutically acceptable derivative is a salt, hydrate or ester.

Assignments (6)
MERGER Recorded May 13, 2016
From: MOUNT SINAI HOSPITAL; BRIDGEPOINT HOSPITAL
To: SINAI HEALTH SYSTEM
Reel/Frame 038593/0787 →
CONFIRMATORY LICENSE Recorded Apr 24, 2012
From: UNIVERSITY OF CALIFORNIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 028094/0852 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2008
From: LAU, KEN SUI-KWONG
To: MOUNT SINAI HOSPITAL
Reel/Frame 021546/0956 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2008
From: DENNIS, JAMES
To: MOUNT SINAI HOSPITAL
Reel/Frame 021546/0969 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2008
From: DEMETRIOU, MICHAEL
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 021548/0052 →
RE-RECORD TO CORRECT THE ASSIGNOR'S NAME ON A DOCUMENT PREVIOUSLY RECORDED AT REEL 021546, FRAME 0956. (ASSIGNMENT OF ASSIGNOR'S INTEREST) Recorded Sep 18, 2008
From: LAU, KEN SIU KWONG
To: MOUNT SINAI HOSPITAL
Reel/Frame 021649/0724 →
Continuity (3)
Provisional Application 60663380 · Mar 17, 2005
Provisional Application 60643962 · Jan 14, 2005
Related Publication 20090099130A1 · Apr 16, 2009