IP Library Granted Patent US 8,715,999
Granted Patent B2
US 8,715,999 · App. 12/866,631 · Granted May 6, 2014

Flaviviridae mutants comprising a deletion in the capsid protein for use as vaccines

Inventors: Franz X. Heinz (Vienna, AT); Christian Mandl (Vienna, AT); Petra Schlick (Vienna, AT); Andreas Meinke (Pressbaum, AT)
Assignee: Valneva Austria GmbH
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Quick Facts
Patent No.
US 8,715,999
App. No.
12/866,631
Granted
May 6, 2014
Kind
B2
Abstract

The present invention relates to a mutant virus of the family flaviviridae, comprising a deletion in the capsid protein of at least 20 successive amino acids, without any further deletion, substitution or insertion mutation except of the amino acids next to the deletion, which may be substituted.

Claims (34)

1. A mutant virus of the flavivirus genus, comprising a capsid protein with a deletion of up to 47 amino acids, wherein the deletion comprises the entire helix 3, and wherein there are no further deletion, substitution or insertion mutations within the capsid protein, with the proviso that amino acids adjacent to the deletion may be substituted.

2. The virus of claim 1 , further defined as an arthropod borne virus.

3. The virus of claim 2 , further defined as a mosquito borne virus.

4. The virus of claim 1 , further defined as yellow fever virus (YFV), Japanese encephalitis virus (JEV), Dengue viruses (DV), tick-borne encephalitis virus (TBE virus), West Nile virus (WNV), Murray Valley encephalitis virus (MVEV), Saint Louis encephalitis virus (SLEV) or Powassan virus (PV).

5. The virus of claim 1 , wherein the deletion is of at least 22 successive amino acids.

6. The virus of claim 5 , wherein the deletion is of at least 24 successive amino acids.

7. The virus of claim 6 , wherein the deletion is of at least 26 successive amino acids.

8. The virus of claim 7 , wherein the deletion is of at least 28 successive amino acids.

9. The virus of claim 8 , wherein the deletion is of at least 30 successive amino acids.

10. The virus of claim 9 , wherein the deletion is of at least 32 successive amino acids.

11. The virus of claim 10 , wherein the deletion is of at least 34 successive amino acids.

12. The virus of claim 1 , wherein the deletion is of up to 46 amino acids.

13. The virus of claim 12 , wherein the deletion is of up to 44 amino acids.

14. The virus of claim 13 , wherein the deletion is of up to 42 amino acids.

15. The virus of claim 14 , wherein the deletion is of up to 40 amino acids.

16. The virus of claim 15 , wherein the deletion is of up to 38 amino acids.

17. The virus of claim 1 , wherein the virus is capable of being passaged in cell culture and genetically stable.

18. The virus of claim 17 , wherein virus is capable of being passaged at least two times in cell culture.

19. The virus of claim 1 , wherein the deletion comprises at least one amino acid of alpha helix 2 of the wild type virus capsid protein.

20. The virus of claim 19 , wherein the deletion comprises at least a third of the amino acids of helix 2.

21. The virus of claim 20 , wherein the deletion comprises the C-terminal amino acids of helix 2.

22. The virus of claim 1 , wherein the deletion comprises at least one amino acid of alpha helix 4 of the wild type virus capsid protein.

23. The virus of claim 22 , wherein the deletion comprises at least one third of the amino acids of helix 4.

24. The virus of claim 23 , wherein the deletion comprises the N-terminal amino acids of helix 4.

25. The virus of claim 1 , further defined as comprising a mutation outside of the capsid protein.

26. A pharmaceutical composition comprising the virus of claim 1 , a capsid protein of that mutated virus, or a nucleic acid encoding a capsid protein of the mutated virus.

27. The pharmaceutical composition of claim 26 , further defined as a vaccine.

28. The pharmaceutical composition of claim 26 , further defined as comprising 10 1 to 10 7 infectious units of said virus.

29. The pharmaceutical composition of claim 28 , further defined as comprising 10 2 to 10 6 infectious units of said virus.

30. The pharmaceutical composition of claim 29 , further defined as comprising 10 3 to 10 5 infectious units of said virus.

31. The pharmaceutical composition of claim 26 , further defined as comprising antibiotics, preservatives, stabilizers, buffer substances or mixtures thereof.

32. The pharmaceutical composition of claim 26 , further defined as comprising an aminoglycoside antibiotic, a liposome, a microsphere or a mixture thereof.

33. The pharmaceutical composition of claim 32 , wherein the aminoglycoside antibiotic is neomycin or kanamycin.

34. The virus of claim 1 , wherein the deletion comprises the entire helix 2.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2014
From: VALNEVA AUSTRIA GMBH
To: HEINZ, FRANZ XAVER; MANDL, CHRISTIAN
Reel/Frame 033645/0243 →
CHANGE OF NAME Recorded Mar 5, 2014
From: INTERCELL AUSTRIA AG
To: VALNEVA AUSTRIA GMBH
Reel/Frame 032354/0679 →
ASSET TRANSFER AGREEMENT Recorded Mar 5, 2014
From: INTERCELL AG
To: INTERCELL AUSTRIA AG
Reel/Frame 032388/0680 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2010
From: HEINZ, FRANZ X.; MANDL, CHRISTIAN; SCHLICK, PETRA; MEINKE, ANDREAS
To: INTERCELL AG
Reel/Frame 024989/0123 →
Priority Claims (1)
EP 08101404 · Feb 8, 2008 · regional
Continuity (1)
Related Publication 20100323003A1 · Dec 23, 2010