IP Library Granted Patent US 12,350,328
Granted Patent B2
US 12,350,328 · App. 17/434,489 · Granted Jul 8, 2025

Multivalent live-attenuated influenza vaccine for prevention and control of equine influenza virus (EIV) in horses

Inventors: Luis Martinez-Sobrido (Rochester, NY); Thomas Chambers (Lexington, KY); Kendall Wayne King (Kalamazoo, MI)
Assignees: University of Rochester; UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION; ZOETIS SERVICES LLC
A61K39/145A61P31/16A61K2039/5254A61K2039/552A61K2039/70
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Quick Facts
Patent No.
US 12,350,328
App. No.
17/434,489
Granted
Jul 8, 2025
Kind
B2
Abstract

The present invention provides compositions and methods related to equine live-attenuated influenza vaccines. In one aspect, the invention relates to a composition comprising a multivalent equine live-attenuated influenza vaccine comprising a first live-attenuated influenza virus expressing one or more antigens of a clade 1 H3N8 equine influenza virus; and a second live-attenuated influenza virus expressing one or more antigens of a clade 2 H3N8 equine influenza virus, wherein the second live-attenuated influenza virus expresses HA, NA, or a combination thereof of A/equine/Lancashire/1/2016 H3N8.

Claims (25)

1. A multivalent immunological composition comprising two or more equine live-attenuated influenza viruses (LAIV), comprising:

a first LAIV expressing one or more antigens of a clade 1 H3N8 equine influenza virus; and

a second LAIV expressing one or more antigens of a clade 2 H3N8 equine influenza virus, wherein the second LAIV expresses hemagglutinin (HA), Neuraminidase (NA), or a combination thereof of A/equine/Lancashire/1/2016 H3N8,

wherein each LAIV comprises one or more mutations in one or more of: segment 1 and segment 2 of the viral genome,

wherein segment 1 of the viral genome encodes a polymerase basic 2 (PB2) protein and segment 2 of the viral genome encodes a polymerase basic 1 (PB1) protein.

2. The composition of claim 1 , wherein the first LAIV expresses HA, NA, or a combination thereof of A/equine/Ohio/1/2003 H3N8.

3. The composition of claim 1 , wherein the first LAIV expresses HA, NA, or a combination thereof of A/equine/Texas/6/2017 H3N8.

4. The composition of claim 1 , wherein segment 1 of the first LAIV and/or the second LAIV comprises the nucleic acid sequence set forth in SEQ ID NO: 1.

5. The composition of claim 1 , wherein segment 2 of the first LAIV and/or the second LAIV comprises the nucleic acid sequence set forth in SEQ ID NO: 3.

6. The composition of claim 1 , wherein at least one LAIV comprises one or more mutations in segment 1, which encodes a mutant PB2.

7. The composition of claim 6 , wherein the mutant PB2 comprises a N265S point mutation relative to SEQ ID NO: 6.

8. The composition of claim 7 , wherein the mutant PB2 comprises the amino acid sequence set forth in SEQ ID NO: 2.

9. The composition of claim 1 , wherein at least one LAIV comprises one or more mutations in segment 2, which encodes a mutant PB1.

10. The composition of claim 9 , wherein the mutant PB1 comprises one or more of: a K391E point mutation relative to SEQ ID NO: 8, an E581G point mutation relative to SEQ ID NO: 8, and/or an A661T point mutation relative to SEQ ID NO: 8.

11. The composition of claim 10 , wherein the mutant PB1 comprises a K391E point mutation relative to SEQ ID NO: 8, an E581G point mutation relative to SEQ ID NO: 8, and an A661T point mutation relative to SEQ ID NO: 8.

12. The composition of claim 11 , wherein the mutant PB1 comprises the amino acid sequence set forth in SEQ ID NO: 4.

13. The composition of claim 1 , wherein each LAIV comprises one or more mutations in segment 1, which encodes a mutant PB2; and one or more mutations in segment 2, which encodes a mutant PB1.

14. The composition of claim 13 , wherein the mutant PB2 comprises a N265S point mutation relative to SEQ ID NO: 6 and wherein the mutant PB1 comprises a K391E point mutation relative to SEQ ID NO: 8, an E581G point mutation relative to SEQ ID NO: 8, and an A661T point mutation relative to SEQ ID NO: 8.

15. The composition of claim 1 , wherein the composition is used for the treatment of equine influenza in a subject.

16. The composition of claim 1 , wherein segment 1 of each LAIV is derived from segment 1 of A/equine/Ohio/1/2003; and wherein segment 2 of each LAIV is derived from segment 2 of A/equine/Ohio/1/2003.

17. A method for inducing an immune response against a plurality of equine influenza viruses in a subject, the method comprising administering to the subject the immunological composition of claim 1 .

18. The method of claim 17 , wherein the subject does not have equine influenza, and wherein the method induces immunity against equine influenza.

19. The method of claim 17 , wherein the subject is infected with equine influenza, and wherein the method induces a therapeutic immune response.

20. The method of claim 17 , wherein the immunological composition is administered intranasally, intratracheally, orally, intradermally, intramuscularly, intraperitoneally, intravenously, or subcutaneously.

21. The method of claim 17 , wherein the subject is a horse.

Continuity (2)
Provisional Application 62811112 · Feb 27, 2019
Related Publication 20220133877A1 · May 5, 2022
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