IP Library Granted Patent US 8,691,239
Granted Patent B2
US 8,691,239 · App. 14/037,222 · Granted Apr 8, 2014

Influenza hemagglutinin and neuraminidase variants

Inventors: Chin-Fen Yang (Zhubei, TW); George Kemble (Saratoga, CA); Chongguang Liu (Fremont, CA)
Assignee: MedImmune, LLC
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Quick Facts
Patent No.
US 8,691,239
App. No.
14/037,222
Granted
Apr 8, 2014
Kind
B2
Abstract

Polypeptides, polynucleotides, methods, compositions, and vaccines comprising influenza hemagglutinin and neuraminidase variants are provided.

Claims (20)

1. A reassortant influenza A virus comprising six internal genome segments from one or more donor viruses and at least one surface antigen genome segment encoding a hemagglutinin (HA) polypeptide comprising the amino acid sequence of SEQ ID NO: 87.

2. The reassortant influenza A virus of claim 1 , further comprising a surface antigen genome segment encoding a neuraminidase (NA) polypeptide comprising the amino acid sequence of SEQ ID NO: 88.

3. The reassortant influenza A virus of claim 1 , wherein the surface antigen genome segment encoding the HA polypeptide comprises the polynucleotide of SEQ ID NO: 39.

4. The reassortant influenza A virus of claim 2 , wherein the surface antigen genome segment encoding the NA polypeptide comprises the polynucleotide of SEQ ID NO: 40.

5. The reassortant influenza A virus of claim 1 , wherein the one or more donor viruses have one or more phenotypes chosen from temperature-sensitive, cold-adapted, and attenuated.

6. The reassortant influenza A virus of claim 1 , wherein the one or more donor viruses are selected from the group consisting of A/Ann Arbor/6/60 and A/Puerto Rico/8/34.

7. The reassortant influenza A virus of claim 1 , wherein the reassortant influenza A virus is a live attenuated reassortant influenza virus.

8. The reassortant influenza A virus of claim 1 , wherein the reassortant influenza A virus is killed or inactivated.

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

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

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

12. A method for stimulating the immune system of an individual to produce an immune response against influenza A virus, the method comprising administering to the individual an immunologically effective amount of the reassortant influenza A virus of claim 5 , which is in a physiologically effective carrier.

13. A method for stimulating the immune system of an individual to produce an immune response against influenza A virus, the method comprising administering to the individual an immunologically effective amount of the reassortant influenza A virus of claim 7 , which is in a physiologically effective carrier.

14. A method for stimulating the immune system of an individual to produce an immune response against influenza A virus, the method comprising administering to the individual an immunologically effective amount of the reassortant influenza A virus of claim 8 , which in a physiologically effective carrier.

15. A method for producing an influenza A virus in cell culture, the method comprising:

i) introducing into a population of cultured host cells, which population of cultured host cells is capable of supporting replication of influenza A virus, a plurality of vectors comprising nucleotide sequences corresponding to at least 6 internal genome segments of one or more donor viruses, and at least one genome segment encoding an HA surface antigen polypeptide, wherein the HA surface antigen polypeptide comprises the amino acid sequence of SEQ ID NO: 87;

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

iii) recovering the influenza A virus.

16. The method of claim 15 , wherein the genome segment encoding the HA surface antigen polypeptide comprises the polynucleotide of SEQ ID NO: 39.

17. The method of claim 15 , wherein the one or more donor viruses have one or more phenotypes chosen from temperature-sensitive, cold-adapted, and attenuated.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2014
From: YANG, CHIN-FEN; KEMBLE, GEORGE; LIU, CHONGGUAN
To: MEDIMMUNE, INC
Reel/Frame 032114/0669 →
CHANGE OF NAME Recorded Feb 1, 2014
From: MEDIMMUNE, INC
To: MEDIMMUNE, LLC
Reel/Frame 032114/0679 →
Continuity (7)
Continuation 13708743 · Dec 7, 2012
Continuation 13329123 · Dec 16, 2011
Division 12858386 · Aug 17, 2010
Continuation 12262215 · Oct 31, 2008
Division 11368246 · Mar 6, 2006
Provisional Application 60659832 · Mar 8, 2005
Related Publication 20140023680A1 · Jan 23, 2014