IP Library Granted Patent US 7,270,827
Granted Patent B2
US 7,270,827 · App. 10/284,400 · Granted Sep 18, 2007

Multivalent streptococcal vaccine compositions and methods for use

Assignees: University of Tennessee Research Foundation; ID Biomedical Corporation of Washington
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Quick Facts
Patent No.
US 7,270,827
App. No.
10/284,400
Granted
Sep 18, 2007
Kind
B2
Abstract

Compositions and methods for making and using therapeutic formulations of multivalent hybrid polypeptides comprising immunogenic peptides of M proteins from various different serotypes of group A streptococci and antibodies thereto are provided. Also provided are nucleic acids encoding such hybrid polypeptides. The hybrid polypeptide formulations may be used, for example, in methods for treating or preventing a microbial infection and eliciting a protective immune response having broadly protective opsonic antibodies in the absence of tissue cross-reactive antibodies.

Claims (19)

1. A composition comprising a pharmaceutically acceptable carrier and a mixture of at least two hybrid polypeptides selected from

(a) a hybrid polypeptide consisting of six different immunogenic amino terminal peptides from six different group A streptococcal M proteins M24, M5, M6, M19, M29 and M14, wherein the six different immunogenic amino terminal peptides are linked in tandem by at least two amino acids, wherein each of the immunogenic amino terminal peptides comprises at least 30 contiguous amino acids of each of said group A streptococcal M proteins, wherein the immunogenic amino terminal peptide at the amino terminus of the hybrid polypeptide is reiterated at the carboxy terminus of the hybrid polypeptide and wherein the hybrid polypeptide is capable of eliciting an immune response against more than one of said group A streptococcal M proteins M5, M6, M14, M19, M24 and M29;

(b) a hybrid polypeptide consisting of seven different immunogenic amino terminal peptides from seven different group A streptococcal M proteins M2, M43, M94, M22, M11, M59 and M33, wherein the seven different immunogenic amino terminal peptides are linked in tandem by at least two amino acids, wherein each of the immunogenic amino terminal peptides comprises at least 35 contiguous amino acids of each of said group A streptococcal M proteins, wherein the immunogenic amino terminal peptide at the amino terminus of the hybrid polypeptide is reiterated at the carboxy terminus of the hybrid polypeptide and wherein the hybrid polypeptide is capable of eliciting an immune response against more than one of said group A streptococcal M proteins M2, M11, M22, M33, M43, M59 and M94;

(c) a hybrid polypeptide consisting of seven different immunogenic amino terminal peptides from seven different group A streptococcal M proteins M89, M101, M77, M114, M75, M76 and M92, wherein the seven different immunogenic amino terminal peptides are linked in tandem by at least two amino acids, wherein each of the immunogenic amino terminal peptides comprises at least 40 contiguous amino acids of each of said group A streptococcal M proteins, wherein the immunogenic amino terminal peptide at the amino terminus of the hybrid polypeptide is reiterated at the carboxy terminus of the hybrid polypeptide and wherein the hybrid polypeptide is capable of eliciting an immune response against more than one of said group A streptococcal M proteins M75, M76, M77, M89, M92, M101 and M114; and

(d) a hybrid polypeptide consisting of seven different immunogenic amino terminal peptides from seven different group A streptococcal proteins M1.0, M12, Spa, M28, M3, M1.2, M18 and M1.0, wherein the seven different immunogenic amino terminal peptides are linked in tandem by at least two amino acids, wherein each of the immunogenic amino terminal peptides comprises at least 50 contiguous amino acids of each of said group A streptococcal proteins, wherein the immunogenic amino terminal peptide at the amino terminus of the hybrid polypeptide is reiterated at the carboxy terminus of the hybrid polypeptide and wherein the hybrid polypeptide is capable of eliciting an immune response against more than one of said group A streptococcal proteins Spa, M1.0, M1.2, M3, M12, M18 and M28.

2. The composition according to claim 1 wherein the at least two hybrid polypeptides are selected from M24-M5-M6-M19-M29-M14-M24, M2-M43-M94-M22-M11-M59-M33-M2, M89-M101 -M77-M114-M75-M76-M92-M89, and M1.0-M12Spa-MM28-M3-M1.2-M18-M1.0.

3. The composition according to claim 1 wherein the mixture comprises the hybrid polypeptide of item (d) and at least one of the hybrid polypeptides of item (a), item (b) and item (c).

4. The composition according to claim 3 wherein the hybrid polypeptide of item (d) is M1.0-M12-Spa-M28-M3-M1.2-M18-M1.0 and wherein the hybrid polypeptide of item (a) is M24-M5-M6-M19-M29-M14-M24, the hybrid polypeptide of item (b) is M2-M43-M94-M22-M11-M59-M33-M2 and the hybrid polypeptide of item (c) is M89-M101-M77-M114-M75-M76-M92-M89.

5. The composition according to claim 1 wherein the mixture comprises at least three hybrid polypeptides according to item (a), item (b), item (c) and item (d).

6. The composition according to claim 5 wherein the mixture comprises at least three hybrid polypeptides selected from M24-M5-M6-M19-M29-M14-M24, M2-M43-M94-M22-M 11-M59-M33-M2, M89-M101-M77-M 114-M75-M76-M92-M89, and M1.0-M12-Spa-M28-M3-M1.2-M18-M1.0.

7. A composition comprising a pharmaceutically acceptable carrier and a mixture of (a) a recombinant hybrid polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 2; (b) a recombinant hybrid polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 4; (c) a recombinant hybrid polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 6; and (d) a recombinant hybrid polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 8.

8. The composition according to claim 7 further comprising an adjuvant.

9. The composition according to claim 8 wherein the adjuvant is selected from the group consisting of aluminum hydroxide (alum), aluminum phosphate, proteosome adjuvant, virosome, liposome, Freund's complete adjuvant, Freund's incomplete adjuvant, and an oil and water emulsion.

10. The composition according to claim 1 wherein the hybrid polypeptide of item (a) is recombinant M24-M5-M6-M19-M29-M14-M24.

11. The composition according to claim 1 wherein the hybrid polypeptide of item (b) is recombinant M2-M43-M94-M22-M11-M59-M33-M2.

12. The composition according to claim 1 wherein the hybrid polypeptide of item (c) is recombinant M89-M101-M77-M114-M75-M76-M92-M89.

13. The composition according to claim 1 wherein the hybrid polypeptide of item (d) is recombinant M1.0-M12-Spa-M28-M3-M1.2-M18-M1.0.

14. The composition according to claim 1 further comprising an adjuvant.

15. The composition according to claim 14 wherein the adjuvant is selected from the group consisting of aluminum hydroxide (alum), aluminum phosphate, proteosome adjuvant, virosome, liposome, Freund's complete adjuvant, Freund's incomplete adjuvant, and an oil and water emulsion.

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2010
From: ID BIOMEDICAL CORPORATION OF WASHINGTON
To: UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION
Reel/Frame 025536/0394 →
CONFIRMATORY LICENSE Recorded Aug 11, 2010
From: UNIVERSITY OF TENNESSEE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024826/0538 →
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Oct 30, 2008
From: UNIVERSITY OF TENNESSEE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021765/0450 →
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Oct 30, 2008
From: UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021765/0208 →
CHANGE OF NAME Recorded Aug 15, 2006
From: UNIVERSITY OF TENNESSEE RESEARCH CORPORATION
To: UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION
Reel/Frame 018107/0360 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2003
From: REDDISH, MARK A.; HU, MARY CHAOHONG; WALLS, MICHAEL A.
To: ID BIOMEDICAL CORPORATION OF WASHINGTON
Reel/Frame 013784/0012 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2003
From: DALE, JAMES B.
To: TENNESSEE RESEARCH CORPORATION, UNIVERSITY OF
Reel/Frame 013785/0180 →
Continuity (2)
Provisional Application 6034843400 · Oct 26, 2001
Related Publication 20030143245A1 · Jul 31, 2003