IP Library Granted Patent US 8,697,085
Granted Patent B2
US 8,697,085 · App. 13/525,020 · Granted Apr 15, 2014

Group A

Inventor: James B. Dale (Memphis, TN)
Assignee: University of Tennessee Research Foundation
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,697,085
App. No.
13/525,020
Granted
Apr 15, 2014
Kind
B2
Abstract

Immunogenic compositions are provided herein that are useful for inducing an immune response specific against group A streptococcus (GAS). Immunogenic compositions provided herein are multivalent and comprise a plurality of immunogenic peptides or fusion polypeptides comprising the immunogenic peptides that induce an immune response against GAS. The immunogenic compositions provided herein induce an immune response against the GAS serotypes represented by an immunogenic peptide (derived from an M protein or Spa protein) comprised within the immunogenic composition and also induce an immune response against serotypes that are unrepresented by any immunogenic peptide included in the immunogenic composition. Methods for using the compositions for inducing an immune response against GAS and for treating or reducing the likelihood of occurrence of a GAS infection are also provided.

Claims (22)

1. An immunogenic composition comprising at least 31 immunogenic peptides, wherein each immunogenic peptide is different and comprises at least 25 contiguous amino acids from the amino terminal portion of a different M protein or Spa protein, wherein each different M protein is independently selected from the M protein of group A streptococcus (GAS) serotype 1, 2, 3, 4, 5, 6, 11, 12, 14, 18, 19, 22, 24, 28, 29, 44, 49, 58, 73, 75, 77, 78, 81, 82, 83, 87, 89, 92, 114, and 118, and the Spa protein is from GAS serotype 18,

wherein the immunogenic composition comprises a first fusion polypeptide, a second fusion polypeptide, a third fusion polypeptide, and a fourth fusion polypeptide that each comprises at least six of the different immunogenic peptides linked in tandem,

wherein the first fusion polypeptide comprises eight of the different immunogenic peptides linked in tandem, wherein each of the eight immunogenic peptides comprises at least 25 contiguous amino acids from the amino terminal portion of a different M protein or the Spa protein, wherein each different M protein is independently selected from the M protein of GAS serotype 1, 2, 3, 6, 12, 18, and 28, and the Spa protein is from GAS serotype 18;

wherein the second fusion polypeptide comprises eight of the different immunogenic peptides linked in tandem, and wherein each of the eight immunogenic peptides comprises at least 25 contiguous amino acids from the amino terminal portion of a different M protein independently selected from the M protein of GAS serotype 4, 5, 11, 14, 19, 24, 29, and 75;

wherein the third fusion polypeptide comprises eight of the different immunogenic peptides linked in tandem, and wherein each of the eight immunogenic peptides comprises at least 25 contiguous amino acids from the amino terminal portion of a different M protein independently selected from the M protein of GAS serotype 22, 44, 58, 73, 77, 78, 89, and 118;

wherein the fourth fusion polypeptide comprises seven of the different immunogenic peptides linked in tandem, and wherein each of the seven immunogenic peptides comprises at least 25 contiguous amino acids from the amino terminal portion of a different M protein independently selected from the M protein of GAS serotype 49, 81, 82, 83, 87, 92, and 114, and wherein the immunogenic composition induces an immune response against GAS.

2. The immunogenic composition of claim 1 , wherein the immunogenic peptide located at the carboxy terminal end of the first fusion polypeptide is a duplicate of the immunogenic peptide located at the amino terminal end of the first fusion polypeptide.

3. The immunogenic composition of claim 2 , wherein the immunogenic peptide that is duplicated comprises at least 25 contiguous amino acids from the amino terminal portion of the M protein of GAS serotype 1.

4. The immunogenic composition of claim 1 , wherein the immunogenic peptide located at the carboxy terminal end of the second fusion polypeptide is a duplicate of the immunogenic peptide located at the amino terminal end of the second fusion polypeptide.

5. The immunogenic composition of claim 4 , wherein the immunogenic peptide that is duplicated comprises at least 25 contiguous amino acids from the amino terminal portion of the M protein of GAS serotype 4.

6. The immunogenic composition of claim 1 , wherein the immunogenic peptide located at the carboxy terminal end of the third fusion polypeptide is a duplicate of the immunogenic peptide located at the amino terminal end of the third fusion polypeptide.

7. The immunogenic composition of claim 6 , wherein the immunogenic peptide that is duplicated comprises at least 25 contiguous amino acids from the amino terminal portion of the M protein of GAS serotype 77.

8. The immunogenic composition of claim 1 , wherein the immunogenic peptide located at the carboxy terminal end of the fourth fusion polypeptide is a duplicate of the immunogenic peptide located at the amino terminal end of the fourth fusion polypeptide.

9. The immunogenic composition of claim 8 , wherein the immunogenic peptide that is duplicated comprises at least 25 contiguous amino acids from the amino terminal portion of the M protein of GAS serotype 83.

10. The immunogenic composition of claim 1 , wherein one or more of the immunogenic peptides comprises the at least 25 contiguous amino acids from the amino terminal portion of the different M protein or the Spa protein in duplicate.

11. The immunogenic composition of claim 1 , further comprising a pharmaceutically acceptable excipient.

12. The immunogenic composition of claim 11 , further comprising a pharmaceutically acceptable adjuvant.

13. The immunogenic composition of claim 1 , wherein the immune response against group A streptococcus comprises an immune response against at least each of GAS 1, 2, 3, 4, 5, 6, 11, 12, 14, 18, 19, 22, 24, 28, 29, 44, 49, 58, 73, 75, 77, 78, 81, 82, 83, 87, 89, 92, 114, and 118 serotypes.

14. The immunogenic composition of claim 1 , wherein one or more of the immunogenic peptides comprises at least 40 contiguous amino acids from the amino terminal portion of the different M protein or the Spa protein.

15. The immunogenic composition of claim 1 , wherein one or more of the immunogenic peptides comprises at least 45 contiguous amino acids from the amino terminal portion of the different M protein or the Spa protein.

16. The immunogenic composition of claim 1 , wherein one or more of the immunogenic peptides comprises at least 50 contiguous amino acids from the amino terminal portion of the different M protein or the Spa protein.

17. A method for inducing an immune response against group A streptococcus in a subject, comprising administering to the subject the immunogenic composition of claim 1 .

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 11, 2017
From: UNIVERSITY OF TENNESSEE HEALTH SCI CTR
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044219/0312 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2012
From: DALE, JAMES B.
To: UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION
Reel/Frame 028893/0550 →
Continuity (3)
Provisional Application 61641448 · May 2, 2012
Provisional Application 61498397 · Jun 17, 2011
Related Publication 20120321657A1 · Dec 20, 2012