IP Library Granted Patent US 10,919,956
Granted Patent B2
US 10,919,956 · App. 10/713,790 · Granted Feb 16, 2021

Polysaccharide vaccine for staphylococcal infections

Inventors: Gerald B. Pier (Brookline, MA); Tomas Maira-Litran (Brookline, MA)
Assignee: The Brigham and Women's Hospital, Inc.
C07K16/1271A61K31/715A61K39/085A61K47/646C08B37/0063A61K39/00A61K2039/6037A61K2039/6087A61K2039/627G01N2400/10
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Quick Facts
Patent No.
US 10,919,956
App. No.
10/713,790
Granted
Feb 16, 2021
Kind
B2
Abstract

The invention relates to compositions of a deacetylated poly N-acetylated glucosamine (dPNAG) of Staphylococci. The dPNAG may be isolated from natural sources or synthesized de novo. The invention also relates to the use of dPNAG as a vaccine for inducing active immunity to infections caused by Staphylococcus aureus, S. epidermidis , other related coagulase-negative or coagulase-positive Staphylococci, and other organisms carrying the ica (intracellular adhesion) locus. The invention further provides methods of use for antibodies directed to dPNAG, particularly for inducing passive immunity to the same class of infections.

Claims (41)

1. A composition comprising

an isolated β-1,6-glucosamine polymer conjugated to a protein or peptide carrier, wherein less than 40% of glucosamine amino groups in the isolated polymer are substituted with acetate, and

wherein the isolated polymer has the structure of

wherein n is an integer that is at least four, wherein R is selected from the group consisting of —NH—CO—CH 3 and —NH 2 .

2. The composition of claim 1 , wherein less than 35%, less than 30%, less than 25%, less than 20%, less than 15%, less than 10% or less than 5% of the glucosamine amino groups are substituted with acetate.

3. The composition of claim 1 , wherein none of the glucosamine amino groups is substituted with acetate.

4. A composition comprising

an isolated β-1,6-glucosamine polymer, wherein less than 40% of glucosamine amino groups in the isolated polymer are substituted with acetate, wherein the composition is sterile, and

wherein the isolated polymer has the structure of

wherein n is an integer that is at least four, wherein R is selected from the group consisting of —NH—CO—CH 3 and —NH 2 , and wherein the isolated polymer is conjugated to a carrier compound through a linker.

5. The composition of claim 1 , wherein the peptide or protein carrier is tetanus toxoid.

6. The composition of claim 4 , wherein the carrier compound is tetanus toxoid.

7. The composition of claim 1 , wherein the composition is sterile.

8. A composition comprising

an isolated β-1,6-glucosamine polymer conjugated to a carrier compound through a linker, wherein less than 40% of glucosamine amino groups in the isolated polymer are substituted with acetate, and

wherein the isolated polymer conjugated to the carrier compound through a linker comprises the following structure:

wherein each of X1, X2, X3, X4, X5 and X6 is either H or the linker, wherein each of Y1, Y2 and Y3 is either OH or the linker, provided only one of said X1, X2, X3, X4, X5, X6, Y1, Y2 or Y3 is the linker, wherein n is an integer that is at least four, and wherein R is selected from the group consisting of —NH—CO—CH 3 and —NH 2 .

9. The composition of claim 8 , wherein only one of said X1, X2, X3, X4, X5 or X6 is the linker.

10. The composition of claim 8 , wherein only one of said Y1, Y2 or Y3 is the linker.

11. A composition comprising

an isolated β-1,6-glucosamine polymer conjugated to a carrier compound, wherein less than 40% of glucosamine amino groups in the isolated polymer are substituted with acetate, and

wherein the isolated polymer conjugated to the carrier compound comprises the following structure:

wherein each of X1, X2, X3, X4, X5 and X6 is either H, the carrier compound, or a linker joined to the carrier compound, wherein each of Y1, Y2 and Y3 is either OH, the carrier compound or a linker joined to the carrier compound, provided only one of said X1, X2, X3, X4, X5, X6, Y1, Y2 or Y3 is the carrier compound or the linker joined to the carrier compound, wherein n is an integer that is at least four, wherein R is selected from the group consisting of —NH—CO—CH 3 and —NH 2 , wherein the carrier compound is a protein or a peptide.

12. An isolated polysaccharide conjugated to a carrier compound comprising

a β-1,6-glucosamine polymer, wherein less than 40% of glucosamine amino groups in the polymer are substituted with acetate, and

wherein the isolated polysaccharide conjugated to the carrier compound has the structure of

wherein each of X1, X2, X3, X4, X5 and X6 is either H, the carrier compound, or a linker joined to the carrier compound, wherein each of Y1, Y2 and Y3 is either OH, the carrier compound or a linker joined to the carrier compound, provided only one of said X1, X2, X3, X4, X5, X6, Y1, Y2 or Y3 is the carrier compound or the linker joined to the carrier compound, wherein n is an integer that is at least four, wherein R is selected from the group consisting of —NH—CO—CH 3 and —NH 2 , wherein the carrier compound is a protein or peptide carrier.

13. The isolated polysaccharide conjugated to the carrier compound of claim 12 , wherein the isolated polysaccharide conjugated to the carrier compound has the structure of

14. The isolated polysaccharide conjugated to the carrier compound of claim 12 , wherein less than 35%, less than 30%, less than 25%, less than 20%, less than 15%, less than 10% or less than 5% of the glucosamine amino groups are substituted with acetate.

15. The isolated polysaccharide conjugated to the carrier compound of claim 12 , wherein none of the glucosamine amino groups is substituted with acetate.

16. The isolated polysaccharide conjugated to the carrier compound of claim 13 , wherein less than 35%, less than 30%, less than 25%, less than 20%, less than 15%, less than 10%, or less than 5% of the glucosamine amino groups are substituted with acetate.

17. The isolated polysaccharide conjugated to the carrier compound of claim 13 , wherein none of the glucosamine amino groups is substituted with acetate.

18. The isolated polysaccharide conjugated to the carrier compound of claim 12 , wherein the isolated polysaccharide has a molecular weight selected from the group consisting of at least 1000 Daltons, at least 1200 Daltons, at least 1500 Daltons, at least 2000 Daltons, at least 2500 Daltons, at least 5000 Daltons, at least 7500 Daltons, at least 10,000 Daltons, at least 25,000 Daltons, at least 50,000 Daltons, at least 75,000 Daltons, and at least 100,000 Daltons.

19. The isolated polysaccharide conjugated to the carrier compound of claim 12 , wherein n is an integer that is in the range of 4-20.

20. The isolated polysaccharide conjugated to the carrier compound of claim 12 , combined with a pharmaceutically acceptable carrier.

21. The isolated polysaccharide conjugated to the carrier compound of claim 12 , wherein the isolated polysaccharide conjugated to the carrier compound is sterile.

22. The composition of claim 12 , wherein the carrier compound is tetanus toxoid.

23. The composition of claim 1 , further comprising a pharmaceutically acceptable carrier.

24. The composition of claim 1 , wherein n is an integer that is in the range of 4-20.

25. The composition of claim 1 , wherein the isolated polymer has a molecular weight of at least 2500 Daltons.

26. The composition of claim 1 , wherein n is 5.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Nov 20, 2009
From: KLP ENTERPRISES LLC
To: ALOPEXX PHARMACEUTICALS LLC
Reel/Frame 023548/0462 →
CONFIRMATORY LICENSE Recorded Jun 18, 2009
From: BRIGHAM AND WOMEN'S HOSPITAL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022841/0162 →
SECURITY AGREEMENT Recorded Feb 8, 2008
From: ALOPEXX PHARMACEUTICALS, LLC
To: KLP ENTERPRISES, LLC
Reel/Frame 020513/0507 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 19, 2004
From: PIER, GERALD B.; MAIRA-LITRAN, TOMAS
To: BRIGHAM AND WOMENS'S HOSPITAL, INC., THE
Reel/Frame 014647/0912 →
Continuity (2)
Provisional Application 60425425 · Nov 12, 2002
Related Publication 20050118198A1 · Jun 2, 2005
Cited By (1)
US 12,397,014