IP Library Granted Patent US 8,293,249
Granted Patent B2
US 8,293,249 · App. 11/796,426 · Granted Oct 23, 2012

Nucleic acid and amino acid sequences relating to

Assignee: Sanofi Pasteur Limited/Sanofi Pasteur Limitee
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Quick Facts
Patent No.
US 8,293,249
App. No.
11/796,426
Granted
Oct 23, 2012
Kind
B2
Abstract

The invention provides isolated polypeptide and nucleic acid sequences derived from Streptococcus pneumoniae that are useful in diagnosis and therapy of pathological conditions; antibodies against the polypeptides; and methods for the production of the polypeptides. The invention also provides methods for the detection, prevention and treatment of pathological conditions resulting from bacterial infection.

Claims (26)

1. An isolated polypeptide comprising the amino acid sequence as set forth in SEQ ID NO: 5326.

2. An isolated polypeptide having at least 80% identity to the amino acid sequence of SEQ ID NO: 5326.

3. An isolated polypeptide having at least 80% identity to the amino acid sequence of SEQ ID NO: 5326, wherein the polypeptide elicits an immune response.

4. The isolated polypeptide of claim 1 , wherein the polypeptide elicits an immune response.

5. The isolated polypeptide of claim 4 , wherein the immune response is an immune response against S. pneumoniae.

6. The isolated polypeptide of claim 2 , wherein the isolated polypeptide has at least 90% identity to SEQ ID NO: 5326.

7. The isolated polypeptide of claim 2 , wherein the isolated polypeptide has at least 95% identity to SEQ ID NO: 5326.

8. The isolated polypeptide of claim 2 , wherein the isolated polypeptide has at least 98% identity to SEQ ID NO: 5326.

9. The isolated polypeptide of claim 2 , wherein the isolated polypeptide has at least 99% identity to SEQ ID NO: 5326.

10. The isolated polypeptide of claim 3 , wherein the immune response is an immune response against S. pneumoniae infection.

11. The isolated polypeptide of claim 3 , wherein the isolated polypeptide has at least 90% identity to SEQ ID NO: 5326.

12. The isolated polypeptide of claim 3 , wherein the isolated polypeptide has at least 95% identity to SEQ ID NO: 5326.

13. The isolated polypeptide of claim 3 , wherein the isolated polypeptide has at least 98% identity to SEQ ID NO: 5326.

14. The isolated polypeptide of claim 3 , wherein the isolated polypeptide has at least 99% identity to SEQ ID NO: 5326.

15. The isolated polypeptide of claim 2 , wherein the polypeptide is a surface protein.

16. The isolated polypeptide of claim 3 , wherein the polypeptide is a surface protein.

17. The isolated polypeptide of claim 2 , wherein the polypeptide provides immunity against S. pneumonia infection.

18. The isolated polypeptide of claim 5 , wherein the polypeptide provides a immune response against S. pneumonia infection.

19. A composition comprising the isolated polypeptide of claim 2 in a pharmaceutically acceptable carrier.

20. The composition of claim 19 , further including an adjuvant.

21. The composition of claim 20 , wherein the adjuvant is at least one member selected from the group consisting of aluminum hydroxide, N-acetyl-muramyl-L-threonyl-D-isoglutamine, N-acetyl-nor-muramyl-L-alanyl-D-isoglutamine, N-acetylmuramyl-L-alanyl-D-isoglutaminyl-L-alanine-2-(1′-2′-dipalmitoyl-sn-glycero-3-hydroxyphos-phoryloxy)-ethylamine; cholera toxin, a non-toxic derivative of cholera toxin, procholeragenoid, fungal polysaccharides, muramyl dipeptide, muramyl dipeptide derivatives, phorbol esters, labile toxin of E. coli , non- S. pneumoniae bacterial lysates, block polymers and saponins.

22. The composition of claim 19 , wherein the isolated polypeptide has at least 90%, 95%, 98% or 99% identity to SEQ ID NO:5326.

23. A composition comprising the isolated polypeptide of claim 3 in a pharmaceutically acceptable carrier.

24. The composition of claim 23 , further including an adjuvant.

25. The composition of claim 24 , wherein the adjuvant is selected from the group consisting of aluminum hydroxide, N-acetyl-muramyl-L-threonyl-D-isoglutamine, N-acetyl-nor-muramyl-L-alanyl-D-isoglutamine, N-acetylmuramyl-L-alanyl-D-isoglutaminyl-L-alanine-2-(1′-2′-dipalmitoyl-sn-glycero-3-hydroxyphos-phoryloxy)-ethylamine; cholera toxin, a non-toxic derivative of cholera toxin, procholeragenoid, fungal polysaccharides, muramyl dipeptide, muramyl dipeptide derivatives, phorbol esters, labile toxin of E. coli , non- S. pneumoniae bacterial lysates, block polymers and saponins.

26. The composition of claim 23 , wherein the isolated polypeptide has at least 90%, 95%, 98% or 99% identity to SEQ ID NO:5326.

Assignments (3)
CHANGE OF NAME Recorded Aug 6, 2012
From: AVENTIS PASTEUR LIMITED/AVENTIS PASTEUR LIMITEE
To: SANOFI PASTEUR LIMITED/SANOFI PASTEUR LIMITEE
Reel/Frame 028734/0586 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2012
From: GENOME THERAPEUTICS CORPORATION
To: AVENTIS PASTEUR LTD
Reel/Frame 028710/0522 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 25, 2012
From: DOUCETTE-STAMM, LYNN; BUSH, DAVID; ZENG, QIANDONG; OPPERMAN, TIMOTHY; HOUSEWEART, CHAD ERIC
To: GENOME THERAPEUTICS CORPORATION
Reel/Frame 028631/0522 →
Continuity (7)
Division 11028458 · Dec 30, 2004
Continuation 10640833 · Aug 14, 2003
Continuation 09583110 · May 26, 2000
Continuation In Part 09107433 · Jun 30, 1998
Provisional Application 60085131 · May 12, 1998
Provisional Application 60051553 · Jul 2, 1997
Related Publication 20080177026A1 · Jul 24, 2008