IP Library › Granted Patent US 9,492,530
Granted Patent B2
US 9,492,530 · App. 14/840,759 · Granted Nov 15, 2016

H3 influenza a virus

Inventors: Christopher W. Olsen (Madison, WI); Gabriele A. Landolt (Fort Collins, CO); Alexander I. Karasin (Madison, WI)
Assignee: Wisconsin Alumni Research Foundation
A61K39/145A61K9/0019A61K9/0043A61K39/12C07K14/005C12N7/00C12R1/91G01N33/56983A61K2039/525A61K2039/5252A61K2039/5254A61K2039/54A61K2039/552C12N2760/16121C12N2760/16122C12N2760/16134G01N2333/11
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Quick Facts
Patent No.
US 9,492,530
App. No.
14/840,759
Granted
Nov 15, 2016
Kind
B2
Abstract

The invention provides an isolated H3 equine influenza A virus, as well as methods of preparing and using the virus, and genes or proteins thereof.

Claims (26)

1. A method of preparing a vaccine, comprising

providing an isolated live H3 influenza virus comprising a gene segment with sequences for a HA having SEQ ID NO: 1 or a HA having at least 98% amino acid sequence identity to SEQ ID NO:1 which HA does not have a valine at position 78 or an asparagine at position 159;

combining the isolated H3 influenza virus with an adjuvant or treating the isolated H3 influenza virus with an agent that inactivates the virus, thereby providing a composition; and

providing an individual dose of the composition comprising an amount effective to immunize a mammal.

2. The method of claim 1 wherein the mammal is a horse.

3. The method of claim 1 wherein the mammal is a canine.

4. The method of claim 1 wherein the composition comprises inactivated virus.

5. The method of claim 1 wherein the H3 influenza virus comprises at least one of the following gene segments: a gene segment with sequences for a NA having SEQ ID NO:2 or having at least 95% amino acid sequence identity to SEQ ID NO:2, a gene segment with sequences for a PB1 having SEQ ID NO:3 or having at least 95% amino acid sequence identity to SEQ ID NO:3, a gene segment with sequences for a PB2 having SEQ ID NO:4 or having at least 95% amino acid sequence identity to SEQ ID NO:4, a gene segment with sequences for a PA having SEQ ID NO:5 or having at least 95% amino acid sequence identity to SEQ ID NO:5, a gene segment with sequences for a NP having SEQ ID NO:6 or having at least 95% amino acid sequence identity to SEQ ID NO:6, a gene segment with sequences for a M1 having SEQ ID NO:7 or having at least 95% amino acid sequence identity to SEQ ID NO:7, a gene segment with sequences for a M2 having SEQ ID NO:17 or having at least 95% amino acid sequence identity to SEQ ID NO: 17, a gene segment with sequences for a NS1 having SEQ ID NO:8 or having at least 95% amino acid sequence identity to SEQ ID NO:8, or a gene segment with sequences for a NS2 having SEQ ID NO: 18 or having at least 95% amino acid sequence identity to SEQ ID NO: 18.

6. The method of claim 1 wherein the composition further comprises a different isolated influenza virus.

7. The method of claim 1 wherein the composition further comprises a pathogen other than the H3 influenza virus.

8. The method of claim 1 wherein the composition comprises the adjuvant.

9. The method of claim 1 further comprises a pharmaceutically acceptable carrier.

10. The method of claim 9 wherein the carrier is suitable for intramuscular administration.

11. The method of claim 1 wherein the composition is freeze-dried.

12. A method of preparing a vaccine, comprising

providing an isolated live H3 influenza virus comprising a gene segment with sequences for a HA having SEQ ID NO: 1 or a HA having at least 95% amino acid sequence identity to SEQ ID NO:1 which HA has an alanine at position 78 and a serine at position 159;

combining the isolated H3 influenza virus with an adjuvant or treating the isolated H3 influenza virus with an agent that inactivates the virus, thereby providing a composition; and

providing an individual dose of the composition comprising an amount effective to immunize a mammal.

13. The method of claim 12 wherein the mammal is a horse.

14. The method of claim 12 wherein the mammal is a canine.

15. The method of claim 12 wherein the composition comprises inactivated virus.

16. The method of claim 12 wherein the carrier is suitable for intranasal administration.

17. The method of claim 12 wherein the composition further comprises a different isolated influenza virus.

18. The method of claim 12 wherein the composition further comprises a pathogen other than the H3 influenza virus.

19. The method of claim 12 wherein the composition comprises the adjuvant.

20. The method of claim 12 further comprising a pharmaceutically acceptable carrier suitable for intramuscular or intranasal administration.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 11, 2016
From: OLSEN, CHRISTOPHER W.; LANDOLT, GABRIELE A.; KARASIN, ALEXANDER I.
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 038543/0222 →
Continuity (5)
Continuation 14255719 · Apr 17, 2014
Continuation 13839111 · Mar 15, 2013
Continuation 12503712 · Jul 15, 2009
Division 11033248 · Jan 11, 2005
Related Publication 20160051662A1 · Feb 25, 2016