IP Library Granted Patent US 7,981,429
Granted Patent B2
US 7,981,429 · App. 12/399,312 · Granted Jul 19, 2011

Influenza hemagglutinin and neuraminidase variants

Assignee: Medimmune, LLC
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Quick Facts
Patent No.
US 7,981,429
App. No.
12/399,312
Granted
Jul 19, 2011
Kind
B2
Abstract

Polypeptides, polynucleotides, methods, compositions, and vaccines comprising (avian pandemic) influenza hemagglutinin and neuraminidase variants are provided.

Claims (39)

1. A reassortant influenza virus, wherein said virus comprises 6 internal genome segments from one or more donor viruses other than A/Ann Arbor/6/60 and a genome segment encoding an immunogenic influenza surface antigen comprising the amino acid sequence of SEQ ID NO: 11.

2. The reassortant influenza virus of claim 1 , wherein the 6 internal genome segments of the one or more donor viruses are selected for comprising one or more phenotypic attributes selected from the group consisting of: attenuated, cold adapted and temperature sensitive.

3. The reassortant influenza virus of claim 1 , wherein said one or more donor viruses are PR8.

4. The reassortant influenza virus of claim 1 , wherein said one or more donor viruses are A/Leningrad/17.

5. An immunogenic composition comprising an immunologically effective amount of the reassortant influenza virus of claim 1 .

6. An immunogenic composition comprising an immunologically effective amount of the reassortant influenza virus of claim 2 .

7. An immunogenic composition comprising an immunologically effective amount of the reassortant influenza virus of claim 3 .

8. An immunogenic composition comprising an immunologically effective amount of the reassortant influenza virus of claim 4 .

9. A method for stimulating the immune system of a subject to produce a protective immune response against influenza virus, the method comprising administering to the subject an immunologically effective amount of the reassortant influenza virus of claim 1 in a physiologically effective carrier.

10. A method for stimulating the immune system of a subject to produce a protective immune response against influenza virus, the method comprising administering to the subject an immunologically effective amount of the reassortant influenza virus of claim 2 in a physiologically effective carrier.

11. A method for stimulating the immune system of a subject to produce a protective immune response against influenza virus, the method comprising administering to the subject an immunologically effective amount of the reassortant influenza virus of claim 3 in a physiologically effective carrier.

12. A method for stimulating the immune system of a subject to produce a protective immune response against influenza virus, the method comprising administering to the subject an immunologically effective amount of the reassortant influenza virus of claim 4 in a physiologically effective carrier.

13. A method of prophylactic or therapeutic treatment of a viral infection in a subject, the method comprising: administering to the subject, the virus of claim 1 in an amount effective to produce an immunogenic response against the viral infection.

14. A method of prophylactic or therapeutic treatment of a viral infection in a subject, the method comprising: administering to the subject, the virus of claim 3 in an amount effective to produce an immunogenic response against the viral infection.

15. A method of prophylactic or therapeutic treatment of a viral infection in a subject, the method comprising: administering to the subject, the virus of claim 4 in an amount effective to produce an immunogenic response against the viral infection.

16. The method of claim 13 , wherein said virus is killed or inactivated.

17. The method of claim 14 , wherein said virus is killed or inactivated.

18. The method of claim 15 , wherein said virus is killed or inactivated.

19. The method of claim 9 , wherein the subject is a human.

20. The method of claim 10 , wherein the subject is a human.

21. The method of claim 11 , wherein the subject is a human.

22. A live attenuated influenza vaccine comprising the composition of claim 5 .

23. A live attenuated influenza vaccine comprising the composition of claim 6 .

24. A split virus or killed virus vaccine comprising the immunogenic composition of claim 5 .

25. A split virus or killed virus vaccine comprising the immunogenic composition of claim 6 .

26. A method for producing influenza viruses in cell culture, the method comprising:

i) introducing into a population of host cells a plurality of vectors comprising nucleic acid sequences corresponding to:

a) at least 6 internal genome segments from a donor virus other than A/Ann Arbor/6/60 and at least one genome segment encoding an immunogenic influenza surface antigen comprising the amino acid sequence of SEQ ID NO: 11; or

b) at least 6 internal genome segments from a donor virus other than A/Ann Arbor/6/60, wherein said donor virus has one or more phenotypic attributes selected from the group consisting of: attenuated, cold adapted and temperature sensitive; and at least one genome segment encoding an immunogenic influenza surface antigen comprising the amino acid sequence of SEQ ID NO: 11;

ii) culturing the population of host cells at a temperature less than or equal to 35° C.; and,

iii) recovering a plurality of influenza viruses.

27. An immunogenic composition comprising an immunologically effective amount of the influenza virus produced by the method comprising:

i) introducing into a population of host cells a plurality of vectors comprising nucleic acid sequences corresponding to:

a) at least 6 internal genome segments from a donor virus other than A/Ann Arbor/6/60 and a genome segment encoding an immunogenic influenza surface antigen comprising the amino acid sequence of SEQ ID NO: 11; or

b) at least 6 internal genome segments from a donor virus other than A/Ann Arbor/6/60, wherein said donor virus has one or more phenotypic attributes selected from the group consisting of: attenuated, cold adapted and temperature sensitive; and a genome segment encoding an immunogenic influenza surface antigen comprising the amino acid sequence of SEQ ID NO: 11;

ii) culturing the population of host cells at a temperature less than or equal to 35° C.; and,

iii) recovering a plurality of influenza viruses.

28. A method for stimulating the immune system of an individual to produce a protective immune response against influenza virus, the method comprising administering to the individual an immunologically effective amount of the influenza virus produced by the method of claim 26 in a physiologically effective carrier.

29. A method for stimulating the immune system of an individual to produce a protective immune response against influenza virus, the method comprising administering to the individual the immunogenic composition of claim 27 .

Assignments (3)
CHANGE OF NAME Recorded Feb 1, 2014
From: MEDIMMUNE VACCINES, INC.
To: MEDIMMUNE, INC.
Reel/Frame 032114/0803 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2014
From: YANG, CHIN-FEN; KEMBLE, GEORGE
To: MEDIMMUNE VACCINES, INC.
Reel/Frame 032114/0810 →
CHANGE OF NAME Recorded Feb 1, 2014
From: MEDIMMUNE, INC.
To: MEDIMMUNE, LLC
Reel/Frame 032114/0822 →
Continuity (4)
Division 11133360 · May 20, 2005
Provisional Application 60574553 · May 25, 2004
Provisional Application 60657554 · Feb 28, 2005
Related Publication 20090175909A1 · Jul 9, 2009