IP Library Granted Patent US 8,722,059
Granted Patent B2
US 8,722,059 · App. 13/214,110 · Granted May 13, 2014

Multi plasmid system for the production of influenza virus

Inventors: Erich Hoffman (Sunnyvale, CA); Hong Jin (Cupertino, CA); Bin Lu (Los Altos, CA); Greg Duke (Redwood City, CA); George Kemble (Saratoga, CA)
Assignee: MedImmune, LLC
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Quick Facts
Patent No.
US 8,722,059
App. No.
13/214,110
Granted
May 13, 2014
Kind
B2
Abstract

Vectors and methods for the production of influenza viruses suitable as recombinant influenza vaccines in cell culture are provided. Bi-directional expression vectors for use in a multi-plasmid influenza virus expression system are provided.

Claims (42)

1. An isolated temperature sensitive recombinant or reassortant influenza B virus, comprising:

a modified NP polypeptide with substitutions consisting of threonine to alanine at position 55, valine to alanine at position 114, proline to histidine at position 410 and alanine to threonine at position 509,

wherein the modified NP polypeptide confers temperature sensitivity to the isolated temperature sensitive recombinant or reassortant influenza B virus.

2. The virus of claim 1 , comprising a PB2 polypeptide that does not include a substitution of serine to arginine at amino acid position 630.

3. The virus of claim 1 , wherein the virus exhibits between about 2.0 and about 4.0 log 10 reduction in growth at 37° C. as compared to a wild type influenza B virus.

4. The virus of claim 1 , which is a 6:2 reassortant influenza B virus.

5. An immunogenic composition comprising the isolated temperature sensitive recombinant or reassortant influenza B virus of claim 1 .

6. A method for stimulating an immune response, which comprises administering the immunogenic composition of claim 5 .

7. A method for making an isolated temperature sensitive recombinant or reassortant influenza B virus of claim 1 , comprising:

(a) introducing mutations in an influenza B virus genome that result in a modified NP polypeptide with substitutions consisting of threonine to alanine at position 55, valine to alanine at position 114, proline to histidine at position 410 and alanine to threonine at position 509;

(b) introducing a plurality of vectors into a population of host cells, wherein the plurality of vectors corresponds to the influenza B virus genome and the plurality of vectors comprises the mutations recited in (a);

(c) culturing the population of host cells; and

(d) recovering recombinant or reassortant influenza B virus produced by the host cells, wherein the recombinant or reassortant influenza B virus is temperature sensitive and the modified NP polypeptide confers temperature sensitivity to virus.

8. An isolated temperature sensitive recombinant or reassortant influenza B virus comprising:

a modified PA polypeptide with substitutions consisting of valine to methionine at position 431 and tyrosine to histidine at position 497;

wherein the modified PA polypeptide confers temperature sensitivity to the isolated temperature sensitive recombinant or reassortant influenza B virus.

9. The virus of claim 8 , comprising a PB2 polypeptide that does not include a substitution of serine to arginine at amino acid position 630.

10. The virus of claim 8 , wherein the virus exhibits between about 2.0 and about 4.0 log 10 reduction in growth at 37° C. as compared to a wild type influenza B virus.

11. The virus of claim 8 , which is a 6:2 reassortant influenza B virus.

12. An immunogenic composition comprising the isolated temperature sensitive recombinant or reassortant influenza B virus of claim 8 .

13. A method for stimulating an immune response, which comprises administering the immunogenic composition of claim 12 .

14. A method for making an isolated temperature sensitive recombinant or reassortant influenza B virus of claim 8 , comprising:

(a) introducing mutations in an influenza B virus genome that result in a modified PA polypeptide with substitutions consisting of valine to methionine at position 431 and tyrosine to histidine at position 497;

(b) introducing a plurality of vectors into a population of host cells, wherein the plurality of vectors corresponds to the influenza B virus genome and the plurality of vectors comprises the mutations recited in (a);

(c) culturing the population of host cells; and

(d) recovering recombinant or reassortant influenza B virus produced by the host cells, wherein the recombinant or reassortant influenza B virus is temperature sensitive and the modified PA polypeptide confers temperature sensitivity to virus.

15. An isolated temperature sensitive recombinant or reassortant influenza B virus comprising:

(i) a modified PA polypeptide with substitutions consisting of valine to methionine at position 431 and tyrosine to histidine at position 497; and

(ii) a modified NP polypeptide with substitutions consisting of threonine to alanine at position 55, valine to alanine at position 114, proline to histidine at position 410 and alanine to threonine at position 509;

wherein the modified PA polypeptide and the modified NP polypeptide confer temperature sensitivity to the isolated temperature sensitive recombinant or reassortant influenza B virus.

16. The virus of claim 15 , comprising a PB2 polypeptide that does not include a substitution of serine to arginine at amino acid position 630.

17. The virus of claim 15 , wherein the virus exhibits between about 2.0 and about 4.0 log 10 reduction in growth at 37° C. as compared to a wild type influenza B virus.

18. The virus of claim 15 , which is a 6:2 reassortant influenza B virus.

19. An immunogenic composition comprising the isolated temperature sensitive recombinant or reassortant influenza B virus of claim 15 .

20. A method for stimulating an immune response, which comprises administering the immunogenic composition of claim 19 .

21. A method for making an isolated temperature sensitive recombinant or reassortant influenza B virus of claim 15 , comprising:

(a) introducing mutations in an influenza B virus genome that result in

(i) a modified PA polypeptide with substitutions consisting of valine to methionine at position 431 and tyrosine to histidine at position 497; and

(ii) a modified NP polypeptide with substitutions consisting of threonine to alanine at position 55, valine to alanine at position 114, proline to histidine at position 410 and alanine to threonine at position 509;

(b) introducing a plurality of vectors into a population of host cells, wherein the plurality of vectors corresponds to the influenza B virus genome and the plurality of vectors comprises the mutations recited in (a);

(c) culturing the population of host cells; and

(d) recovering recombinant or reassortant influenza B virus produced by the host cells, wherein the recombinant or reassortant influenza B virus is temperature sensitive and the modified PA polypeptide and the modified NP polypeptide confer temperature sensitivity to virus.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2014
From: HOFFMAN, ERICH; JIN, HONG; LU, BIN; DUKE, GREG; KEMBLE, GEORGE
To: MEDIMMUNE VACCINES, INC
Reel/Frame 032114/0712 →
CHANGE OF NAME Recorded Feb 1, 2014
From: MEDIMMUNE VACCINES, INC
To: MEDIMMUNE, INC.
Reel/Frame 032114/0722 →
CHANGE OF NAME Recorded Feb 1, 2014
From: MEDIMMUNE, INC.
To: MEDIMMUNE, LLC
Reel/Frame 032114/0729 →
Continuity (9)
Continuation 10423828 · Apr 25, 2003
Provisional Application 60375675 · Apr 26, 2002
Provisional Application 60394983 · Jul 9, 2002
Provisional Application 60410576 · Sep 12, 2002
Provisional Application 60419802 · Oct 18, 2002
Provisional Application 60420708 · Oct 23, 2002
Provisional Application 60457699 · Mar 24, 2003
Provisional Application 60462361 · Apr 10, 2003
Related Publication 20120020997A1 · Jan 26, 2012