H3 influenza A virus
US-9180181-B2 · Nov 10, 2015 · US
US9492530B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9492530-B2 |
| Application number | US-201514840759-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 31, 2015 |
| Priority date | Jan 11, 2005 |
| Publication date | Nov 15, 2016 |
| Grant date | Nov 15, 2016 |
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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.
Opening claim text (preview).
What is claimed is: 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.
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