IP Library Granted Patent US 9,550,814
Granted Patent B2
US 9,550,814 · App. 14/918,417 · Granted Jan 24, 2017

Multiple variants of meningococcal protein NMB1870

Inventors: Maurizio Comanducci (Siena, IT); Mariagrazia Pizza (Siena, IT)
Assignee: GlaxoSmithKline Biologicals SA
C07K14/22A61K39/095A61K39/102A61K39/39C07K14/285A61K2039/55505C07K2319/00
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Quick Facts
Patent No.
US 9,550,814
App. No.
14/918,417
Granted
Jan 24, 2017
Kind
B2
Abstract

Meningococcal protein NMB 1870 has been described in the prior art. The inventors have found that NMB 1870 is an effective antigen for eliciting anti-meningococcal antibody responses, and that it is expressed across all meningococcal serogroups. Forty-two different NMB 1870 sequences have been identified, and these group into three variants. Serum raised against a given variant is bactericidal within the same variant group, but is not active against strains which express one of the other two variants i.e. there is intra-variant cross-protection, but not inter-variant cross-protection. For maximum cross-strain efficacy, therefore, the invention uses mixture comprising different variants of NMB 1870.

Claims (39)

1. A composition comprising an aluminum salt adjuvant, a histidine buffer, and consisting of two purified antigens, wherein the two purified antigens are selected from the group consisting of:

(a) a first purified protein, comprising an amino acid sequence having at least 85% sequence identity to SEQ ID NO: 24;

(b) a second purified protein, comprising an amino acid sequence having at least 85% sequence identity to SEQ ID NO: 33; and

(c) a third purified protein, comprising an amino acid sequence having at least 85% identity to SEQ ID NO: 41, wherein: the first purified protein has less than 70% sequence identity to the second purified protein; the first purified protein has less than 70% sequence identity to the third purified protein; and the second purified protein has less than 70% sequence identity to the third purified protein.

2. The composition of claim 1 , wherein one or both of the purified proteins is a lipoprotein.

3. The composition of claim 1 , wherein at least one of the two purified proteins does not include the amino acid sequence TRSKP (SEQ ID NO: 70) or TRSKPV (SEQ ID NO: 71) within 10 amino acids of its N-terminus.

4. The composition of claim 1 , wherein at least one of the two purified proteins does not include the amino acid sequence PSEPPFG (SEQ ID NO: 72) within 10 amino acids of its N-terminus.

5. The composition of claim 1 , wherein at least one of the two purified proteins includes the amino acid sequence GGGG (SEQ ID NO: 73).

6. The composition of claim 1 , wherein at least one of the two purified proteins is used in the form of a fusion protein.

7. The composition of claim 6 , wherein the fusion protein includes SEQ ID NO: 46 or the Haemophilus influenzae P4 lipoprotein leader sequence.

8. A composition comprising an aluminum salt adjuvant, a histidine buffer, and consisting of two purified antigens, wherein the two purified antigens are selected from the group consisting of:

(a) a first purified protein comprising an amino acid sequence consisting of a fragment of at least 20 contiguous amino acids from SEQ ID NO: 24;

(b) a second purified protein comprising an amino acid sequence consisting of a fragment of at least 20 contiguous amino acids from SEQ ID NO: 33; and

(c) a third purified protein comprising an amino acid sequence consisting of a fragment of at least 20 contiguous amino acids from SEQ ID NO: 41, wherein: the first purified protein has less than 70% sequence identity across its full length to the second purified protein; the first purified protein has less than 70% sequence identity across its full length to the third purified protein; and

the second purified protein has less than 70% sequence identity across its full length to the third purified protein.

9. The composition of claim 8 , wherein one or both of the purified proteins is a lipoprotein.

10. The composition of claim 8 , wherein at least one of the two purified proteins does not include the amino acid sequence TRSKP (SEQ ID NO: 70) or TRSKPV (SEQ ID NO: 71) within 10 amino acids of its N-terminus.

11. The composition of claim 8 , wherein at least one of the two purified proteins does not include the amino acid sequence PSEPPFG (SEQ ID NO: 72) within 10 amino acids of its N-terminus.

12. The composition of claim 8 , wherein at least one of the two purified proteins includes the amino acid sequence GGGG (SEQ ID NO: 73).

13. The composition of claim 8 , wherein at least one of the two purified proteins is used in the form of a fusion protein.

14. The composition of claim 13 , wherein the fusion protein includes SEQ ID NO: 46 or the Haemophilus influenzae P4 lipoprotein leader sequence.

15. A composition comprising an aluminum salt adjuvant, a histidine buffer, and consisting of two purified antigens, wherein the two purified antigens are:

(a) a first purified protein, comprising an amino acid sequence having at least 85% sequence identity to SEQ ID NO: 24; and

(b) a second purified protein, comprising an amino acid sequence having at least 85% sequence identity to SEQ ID NO: 33, wherein the first purified protein has less than 70% sequence identity to the second purified protein.

16. The composition of claim 15 , wherein one or both of the purified proteins is a lipoprotein.

17. The composition of claim 15 , wherein at least one of the two purified proteins does not include the amino acid sequence TRSKP (SEQ ID NO: 70) or TRSKPV (SEQ ID NO: 71) within 10 amino acids of its N-terminus.

18. The composition of claim 15 , wherein at least one of the two purified proteins does not include the amino acid sequence PSEPPFG (SEQ ID NO: 72) within 10 amino acids of its N-terminus.

19. The composition of claim 15 , wherein at least one of the two purified proteins includes the amino acid sequence GGGG (SEQ ID NO: 73).

20. The composition of claim 15 , wherein at least one of the two purified proteins is used in the form of a fusion protein.

21. The composition of claim 20 , wherein the fusion protein includes SEQ ID NO: 46 or the Haemophilus influenzae P4 lipoprotein leader sequence.

22. A composition comprising an aluminum salt adjuvant, a histidine buffer, and consisting of two purified antigens, wherein the two purified antigens are:

(a) a first purified protein comprising an amino acid sequence consisting of a fragment of at least 20 contiguous amino acids from SEQ ID NO: 24;

(b) a second purified protein comprising an amino acid sequence consisting of a fragment of at least 20 contiguous amino acids from SEQ ID NO: 33, wherein the first purified protein has less than 70% sequence identity across its full length to the second purified protein.

23. The composition of claim 22 , wherein one or both of the purified proteins is a lipoprotein.

24. The composition of claim 22 , wherein at least one of the two purified proteins does not include the amino acid sequence TRSKP (SEQ ID NO: 70) or TRSKPV (SEQ ID NO: 71) within 10 amino acids of its N-terminus.

25. The composition of claim 22 , wherein at least one of the two purified proteins does not include the amino acid sequence PSEPPFG (SEQ ID NO: 72) within 10 amino acids of its N-terminus.

26. The composition of claim 22 , wherein at least one of the two purified proteins includes the amino acid sequence GGGG (SEQ ID NO: 73).

27. The composition of claim 22 , wherein at least one of the two purified proteins is used in the form of a fusion protein.

28. The composition of claim 27 , wherein the fusion protein includes SEQ ID NO: 46 or the Haemophilus influenzae P4 lipoprotein leader sequence.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2016
From: COMANDUCCI, MAURIZIO; PIZZA, MARIAGRAZIA
To: CHIRON S.R.L.
Reel/Frame 039292/0296 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2016
From: NOVARTIS VACCINES & DIAGNOSTICS SRL
To: NOVARTIS AG
Reel/Frame 039292/0419 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2016
From: NOVARTIS AG
To: GLAXOSMITHKLINE BIOLOGICALS SA
Reel/Frame 039292/0434 →
CHANGE OF NAME Recorded Jul 29, 2016
From: CHIRON S.R.L.
To: NOVARTIS VACCINES AND DIAGNOSTICS S.R.L.
Reel/Frame 039507/0313 →
Priority Claims (1)
GB 0227346.4 · Nov 22, 2002 · national
Continuity (3)
Continuation 13367289 · Feb 6, 2012
Continuation 10536215
Related Publication 20160039887A1 · Feb 11, 2016