Universal influenza vaccine

Abstract

Immunogenic compositions for inducing a universal immune response to influenza, and particularly influenza A, by eliciting anti-neuraminidase antibodies which provide protection against heterologous influenza infection. Compositions comprising recombinant baculovirus expression vectors expressing neuraminidase in cultured insect cells dispersed in a pharmaceutically-acceptable carrier comprising insect cell culture media, and optional adjuvant. Methods of inducing immune responses against influenza, and particularly influenza A, by eliciting anti-neuraminidase antibodies in a host animal susceptible to infection.

Description

UNIVERSAL INFLUENZA VACCINE CROSS-REFERENCE TO RELATED APPLICATIONS The present application claims the priority benefit of U.S. Provisional Patent Application 5 Serial No. 62 / 778,409, filed December 12, 2018, entitled UNIVERSAL INFLUENZA VACCINE. SEQUENCE LISTING The following application contains a sequence listing in computer readable format (CRF), submitted as a text file in ASCII format entitled "Sequence_ Listing," created on December 6, 20 I 9, 10 as 31 KB. BACKGROUND Field of the Invention The present disclosure relates to vaccines against influenza, and particularly influenza A, 15 which elicit anti-neuraminidase antibodies. Description of Related Art Swine influenza (SI) is an acute respiratory disease caused by influenza A viruses, which is an enveloped virus of the Orthomyxoviridae family. Swine influenza virus (SIV) is both a 20 pathogen of economic significance to the swine industry. An additional concern regarding SIV is its zoonotic potential as under certain circumstances it can be transmitted to humans, which is best exemplified by the 2009 HIN 1 pandemic originated from a swine source. For that reason, it is a high priority agent in animal health for the USDA. A typical outbreak of respiratory disease caused by SIV is characterized by sudden onset 25 and rapid spread within a herd. Clinical symptoms associated with SI may include coughing, sneezing, nasal discharge, elevated rectal temperature, lethargy, breathing difficulty, and depressed appetite. While morbidity rates may reach I 00% with SIV infections, mortality rates are generally low. The genome of SIV is separated into 8 independent RNA segments that allows for frequent 30 reassortment when two different viruses infect and replicate within the same cell of a pig. Reassortment often results in the production of a new influenza virus (antigenic shift), which renders the current strain-specific vaccine strategy ineffective. In addition, influenza A virus has the unique capacity to undergo genetic variations (antigenic drift) in that it can mutate up to 50% CA 3064760 2019-12-12 of the amino acid sequence of its major surface protein, hemagglutinin (HA), without changing the function of the HA protein. Antigenic drift and antigenic shift contribute to apparent failures of SI vaccines when used in the swine industry. In the USA, HIN], HIN2 and H3N2 subtypes are the major causes of SI outbreaks, 5 although other subtypes have been isolated from diseased pigs. Each subtype also consists of several genetic and antigenic clusters. The contemporary H3N2 SIV strain is a triple reassortant strain, resulting from contributions of human, avian, and SI viral lineages. H3N2 is widely spread in U.S. swine herds. A similar reassortment mechanism resulted in the emergence and rapid spread of a triple reassortant HINI virus that has also become endemic in U.S. swine populations. 10 Currently available SI vaccines are based on killed viruses containing HlNI, H1N2 and H3N2 subtypes. Due to antigenic drift and shift, the killed vaccines are very limited in offering protection against SIV strains genetically and antigenically different from the vaccine strains. These killed vaccines appear also to be associated with disease enhancement in vaccinated pigs under some circumstances after virus infection. 15 Nevertheless, vaccination remains the most effective approach to prevent influenza epidemics. Conventional influenza vaccines can prevent clinical disease, but their efficacy depends on the extent of antigenic "match" between the strains used for vaccine preparation and those circulating in the population. This challenge has focused numerous efforts towards discovering a vaccine candidate that elicits a broad-spectrum protection against diverse influenza 20 subtypes, also termed a universal vaccine. Influenza A virus has two large surface glycoproteins, HA and neuraminidase (NA). The HA mediates the viral receptor binding and entry process, while the NA catalytically drives the release of newly formed virus particles as well as promotes the movement of virus particles via mucosa! surfaces. 25 While several commercial inactivated whole-virus, as well as autogenous vaccines, are widely used, efficacy in field conditions is often lacking due to genetic mismatch between vaccine strains and challenge virus. The immune response following vaccination is largely humoral and directed almost exclusively against the immunodominant HA gene. While antibodies recognizing the HA are often neutralizing and can confer sterilizing immunity, mismatch between antibodies 30 and virus can lead to a loss of binding or even enhancement of disease, a phenomenon referred to vaccination associated-enhancement of respiratory disease (V AERO). Numerous studies have shown that NA-specific antibodies are effective in offering protection from influenza by blocking viral particle release. NA as an important target for control, 2 CA 3064760 2019-12-12 and prevention of influenza A virus infection has been demonstrated by FDA-approved therapeutic antiviral drugs like Oseltamivir and Zanamivir (NA inhibitors). The viral NA differs from viral HA in that the NA protein is relatively more conserved than HA among different influenza strains and swine and human isolates principally consist of two major subtypes, termed Nl and N2. 5 Currently marketed influenza vaccines contain an NA component (among other viral particles) but are generally incapable of inducing protective anti-NA antibodies largely due to the immunodominance of the viral HA protein that is also contained in such vaccines. Despite being a viral surface glycoprotein like HA, the natural immune response directed towards NA is substantially less than that of HA. As a consequence, NA exhibits less variability than HA and 10 represents a more conserved antigen. More prominent presentation of NA to the immune system, either by dissociation of the virion or by recombinant expression of NA, has been shown to elicit a stronger anti-NA antibody response. Both the HA and NA proteins are critical to the influenza virus life cycle. HA allows the virus to bind to cell surface sialic acids present on cellular membrane proteins, leading to 15 endocytosis and virus internalization. In contrast, NA cleaves sialic acids from the host cell allowing mature virions to release and disseminate. While HA antibodies can ideally prevent infection, NA antibodies allow cell infection but prevent virus dissemination. This allows for a more robust immune response as antigen can be processed via both MHCI and MHCII, effectively stimulating infection immunity. 20 The baculovirus expression system is widely used for vaccine production. Examples in humans include vaccines for human papillomavirus and influenza virus, while in pigs baculovirus is used for numerous porcine circovirus type 2 vaccines. Baculovirus expression is popular for vaccine antigen production owing to several features. Baculoviruses can only infect certain insects, making them extremely safe for use in mammals. Large amounts of antigen can also easily 25 be produced using baculovirus expression systems, making them economical. SUMMARY OF INVENTION Immunogenic compositions for inducing a universal immune response to influenza. The composition comprises recombinant baculovirus expression vectors in cultured insect cells 30 dispersed in a pharmaceutically-acceptable carrier comprising insect cell culture media and optional adjuvant. The recombinant baculovirus expression vectors express NA. Preferably, the NA is a recombinantly-expressed wild-type NA protein. Kits for stimulating a universal immune response against influenza infection are also 3 CA 3064760 2019-12-12 described. The kits comprise an immunogenic composition according to any one of the embodiments described herein and instructions for administering the composition to a host animal susceptible to influenza. Also described herein are methods of stimulating a universal immune response against 5 influenza infection. The methods comprise administering an immunogenic composition according to any one of the embodiments described herein to a host animal susceptible to influenza in an effective amount. Advantageously, the immunogenic compositions provide a "universal" immune response in that the anti-NA antibodies stimulated by the vaccine provide protection against heterologous influenza infections (i.e., infections from other strains which are different from the 10 strain from which the recombinantly-expressed NA is derived). BRIEF DESCRIPTION OF THE ORA WINGS FIG. I is a graph demonstrating activity ofNA expressed in the recombinant baculovirus expression system. 15 FIG. 2 is a graph showing the IDEXX IAV-S NP ELISA and NA inhibition (NI) titers in sera collected from pigs on the day of challenge. FIG. 3 is a graph of the qRT-PCR Ct values for Ct values in nasal swabs collected from pigs on days I, 3 and 5 post-challenge. FIG. 4 is a graph of the SIV titers (TCID50 / mL) in nasal swabs collected from pigs on days 20 1, 3 and 5 post challenge. FIG. 5 is a graph of qRT-PCR Ct values and percent lung consolidation day 5 post challenge. FIG. 6 is a graph of the pathology scores from lung tissue staining. FIG. 7 is a graph of the results of the NA inhibition assay showing antibody generated to 25 NI and N2. FIG. 8 is a graph of PCR results from lung tissue collected 5 days post-challenge with heterologous HlNl. FIG. 9 is graph of gross and microscopic pathology scores on lungs collected 5 days post challenge. 30 FIG. 10 shows images from SDS-PAGE and Western blotting of purified NAI and NA2 proteins. FIG. 11 is a graph of Serology-NA inhibition (NI) antibody titer to parental viruses. FIG. 12 is a graph of IAV PCR (Ct) values on nasal swabs collected on days 1, 2 and 5 4 CA 3064760 2019-12-12 post challenge and lung tissue collected day 5 post challenge. FIG. 13 is a graph of gross and microscopic scores on lung tissue collected day 5 post challenge. FIG. 14 is a graph of Serology-NA inhibition (NI) antibody titer to parental viruses. 5 FIG. 15 is a graph of IA V PCR (Ct) values on nasal swabs collected on days 3 and 5 post challenge and lung tissue collected day 5 post challenge. FIG. 16 a graph of gross and microscopic scores on lung tissue collected day 5 post challenge. FIG. 17 is a graph of Serology-NA inhibition (NI) antibody titer to parental viruses for 10 diluted vaccine formulations. 15 FIG. 18 shows graphs scoring gross lung lesions after challenge for pigs vaccinated with diluted vaccine formulations. FIG. 19 shows a graph oflHC and H&E staining on lung tissue from pigs vaccinated with diluted vaccine formulations. DETAILED DESCRIPTION Our universal influenza vaccine strategy is to develop a recombinantly-expressed neuraminidase-based protective vaccine for influenza virus, such as against SI, produced in a baculovirus expression system. Baculovirus expression systems and baculovirus expression 20 vectors in general have been described extensively in the literature, including U.S. Patent No. 4,745,051, O'Reilly at al. (Baculovirus Expression Vectors, A Laboratory Manual. (1993)), and Murhammer (Baculovirus and Insect Cell Expression Protocols. In: Methods in Molecular Biology™. Volume 388 (2007)). Immunogenic compositions are described herein which comprise recombinant baculovirus 25 expression vectors in cultured insect cells dispersed in cell culture media, along with an optional adjuvant (oil-in-water, water-in-oil, etc.). The baculovirus expression vectors direct the expression of native or wild-type NA proteins in the infected insect cells. That is, unlike previous approaches using modified NA proteins, such as those in which the transmembrane domain has been modified or deleted, the present expression systems are engineered in a way that the full-length, wild-type 30 or native NA protein sequence is expressed in the system (and not a truncated version), and more particularly the native or wild-type NA protein is expressed as part of the insect cell membrane proteins, and can be found integrated into the insect cell membranes, as well as in the budded baculovirus membranes in the culture supematants. Preferably, the full-length, wild-type / native 5 CA 3064760 2019-12-12 NA coding sequence ( cDNA) is cloned into the baculovirus system for expression. It will be appreciated that such sequences can be identified based upon the circulating strains isolated in a population at a given time, and synthesized to create updated vaccines targeted to circulating strains. However, as shown in the data, the inventive vaccines provide protection against 5 heterologous challenge. Therefore, protective immunity may be obtained even from vaccines different from the circulating strains. Advantageously, since the expression systems are engineered to express the full-length, wild-type / native NA protein, which is associated with and presented by membrane components in the expression system (i.e., the infected insect cells and the baculoviral components), and not as free, soluble recombinant NA in solution, it is believed 10 that the expressed NA protein in the inventive vaccine is presented to the immune system in a manner (folded structure) more closely resembling (and perhaps substantially similar to) its native conformation, further enhancing the immune response. Crude and unpurified cultures of the expression system components are preferably used for the immunogenic compositions, that is, as a crude cell culture containing the unpurified infected 15 cells (presenting NA), baculovirus (expressing NA), and cell media, along with optional adjuvant. In other words, the infected cell culture may be chemically inactivated, but is not otherwise processed or purified. Exemplary insect cells for use in the invention include Lepidopteran species Spodoptera frugiperda and cell lines derived therefrom. Other insect cell hosts can be used including 20 Trichplusia ni, Bombyx mori, cell lines derived therefrom, and the like. Particularly preferred insect cell lines include SF9 (and variants), SF21, High Five (BTI-TN-SBI-4), and the like. Any suitable culture media can be used to propagate the cells. Culture media suitable for insect cell culture is preferably serum-free, and various formulations are known in the art and widely available, such as SF9001I. In general, the culture medium will comprise a mixture of amino acids, 25 sugars, salts, proteins, and the like. Publicly available formulations such as Grace's media are also suitable. Various baculovirus expression systems are commercially available. Exemplary baculovirus expression vectors will generally include ProEasy (AB Vector), BaculoGold™ DNA (PharMingen), Bac-N-Blue™ DNA (lnvitrogen), or BacPAK6™ DNA (Clontech) for cotransfection with the transfer vector (donor or shuttle) plasmid DNA containing the foreign gene. 30 Alternatively, insect cells are transfected with a recombinant bacmid DNA constructed by transposition of the donor plasmid DNA in E. coli cells, using the Bae-to-Bae™ (lnvitrogenGibco / Life Technologies) system. Multiple gene transfer vectors, such as pAcAB3 and pAcAB4 are particularly preferred. 6 CA 3064760 2019-12-12 Favorable baculovirus expression vectors utilize double recombination between the multiple gene transfer vector and baculovirus genomic DNA which is linearized by Bsu36.I such that a portion of the essential gene ORF 1629 is lost due to genomic DNA digestion. Double recombination between the transfer vector and the linearized baculovirus DNA restores ORF1629 5 and concurrently mediates integration of the heterologous gene expression cassette into the baculovirus genome. A further favorable feature of this system is the utilization of baculovirus genomic DNA derived from a baculovirus strain carrying a conditionally-lethal gene which is lost via linearization with Bsu36.I. This feature ensures that any contaminating uncut parental baculovirus DNA does not lead to rescue of parental virus, ensuring that all rescued baculoviruses IO are derived from recombination with the transfer vector. The various components of the immunogenic composition will be selected to be pharmaceutically acceptable. As used herein, the term "pharmaceutically acceptable" means not biologically or otherwise undesirable, in that it can be administered to a subject without excessive toxicity, irritation, or allergic response, and does not cause unacceptable biological effects or 15 interact in a deleterious manner with any of the other components of the composition in which it is contained. A pharmaceutically-acceptable carrier would naturally be selected to minimize any degradation of the baculovirus, insect cells, and other components and to minimize any adverse side effects in the subject, as would be well known to one of skill in the art. Pharmaceuticallyacceptable ingredients include those acceptable for veterinary use as well as human pharmaceutical 20 use, and will depend on the route of administration. Native / wild-type NA proteins are recombinantly expressed at high levels in the insect cells infected with the baculovirus expression vectors. Advantageously, the primary gene product is unprocessed, full length NA which remains associated with the cell membrane of infected insect cells, as well as budded baculovirus membranes. As such, unlike purified or soluble forms of NA, 25 such as those which have been modified or mutated, the NA in the inventive compositions is presented on the surface of such membranes and complexes, likely contributing to the immunogenicity of the composition (particularly as displayed on the baculovirus viral membrane surface) as discussed herein. Expression plasmids can be generated using sequence information for NA, based upon 30 publicly available sequences and / or based upon newly sequenced circulating strains. Exemplary NA sequences include Genbank accessions KYI l 5564 and KU752376, or conservatively modified variants thereof that retain the functionality of NA, or sequences which encode for NA protein, such as Genbank accessions APGS6794. l and AMP44884. l, or conservatively modified 7 CA 3064760 2019-12-12 variants thereof that retain the functionality of NA. It will be appreciated that wild-type / native NA sequences for use as vaccines in various species can be identified from publicly available sequences and / or from circulating strains, such that up-to-date vaccines can be developed. The identified sequences are synthesized into cDNA and inserted or cloned into the baculovirus 5 expression vectors along with appropriate control sequences, promoters, etc. The resulting expression vectors can then be transfected into appropriate insect cells, and the crude culture can be used for vaccine production. Ideally, the immunogenic compositions will include a mixture of two or more NA protein subtypes to provide multi-valent protection. However, this will also depend on the species to be 10 vaccinated. For example, pigs are known to be infected with both NI and N2 strains. However, dogs are more likely to be infected with only N2. Thus, for certain species, only one NA protein subtype may be necessary to achieve vaccination. The platform developed is exemplified in pigs in the working examples, where we have developed the BacNA 1 expression construct that was used in our studies. NAI (SEQ ID NO:2) is derived from A / swine / Iowa / A0l782229 / 2016 HINI 15 (SEQ ID NO:l). We also generated a BacNA2 expression plasmid derived from A / swine / Oklahoma / A0I 730659 / 2016 HIN2 (SEQ ID NO:3). As noted above, suitable baculovirus expression shuttle vectors, such as pAcAB3, are commercially available. However, it will be appreciated that the vaccine platform can be applied to a variety of other species susceptible to influenza infection, including poultry, canines, equines, and felines, as well as humans. 20 In one or more embodiments concerned with research and study, a baculovirus secretion signal sequence (e.g., GP67) and affinity tag (e.g., polyhistidine-tag) can be added to the NA gene during synthesis to facilitate secretion of the protein into the supernatant during cell culture (which is useful for study and research of the secreted protein by affinity chromatography). Isolation and purification from culture medium for research and study is considerably easier than purification 25 from cell lysates, as cellular material does not need to be removed from the preparation. However, for vaccine preparation, baculoviruses expressing native NA proteins can be prepared by gently mix plasmid DNA (e.g., pAcAB3 shuttle vector containing NAI or NA2) and linearized baculovirus DNA (purchased from ABVECTOR) followed by adding Profectin (ABVECTOR) dropwise into the mixture. After a IO-minute incubation, DNA-Profectin mixture 30 will be added into semi-confluent monolayer of insect cells (e.g., SF9) for an additional 72-hours of incubation. Following the confirmation of NA I and NA2 protein expression in Western-blot and NA activity assays, seed virus stocks (BacNAl and NacNAl) can be titrated and optimized in terms of the infectious dose and culture time. The cell culture can be inactivated using an 8 CA 3064760 2019-12-12 appropriate chemical treatment, such as with formaldehyde, P-propiolactone, ethylenimine, binary ethylenimine, or thimerosal (and preferably binary ethylenimine). Preferably, the antigenic influenza components in the immunogenic compositions according to the invention consist of influenza NA-type proteins. That is, the immunogenic 5 compositions are preferably substantially free of other influenza proteins, subunits, particles, etc., such as influenza HA, matrix proteins (Ml or M2), RNA polymerase subunits PBI, PB2, and PA~ nucleoprotein (NP), nonstructural proteins (NS 1, NS2), or associated virus like particles. As used here, Hsubstantially free" means that the component is not intentionally added or part of the composition, although it is recognized that residual or incidental amounts or impurities may be 10 present in low amounts ( e.g., less than about 0.1 % by weight and preferably less than about 0.0 I% by weight, based upon the total weight of the composite taken as 100% by weight). That is, the only influenza antigenic component(s) present in the inventive compositions is NA (and preferably mixtures of NAI and NA2). More preferably, the recombinantly-expressed NA proteins in the vaccine are membrane-bound or membrane-associated, full-length, or native NA proteins (as 15 opposed to free, soluble, modified NA proteins). The immunogenic compositions can comprise a therapeutically effective amount of NA dispersed in a suitable carrier. Examples include aqueous solutions such as sterile water / distilled autoclaved water (DAW), phosphate buffered saline (PBS), normal (n.) saline (~0.9% NaCl), aqueous dextrose solutions, aqueous glycerol solutions, ethanol, normal allantoic fluid, various 20 oil-in-water or water-in-oil emulsions, as well as dimethyl sulfoxide (DMSO) or other acceptable vehicles, and the like. In the inventive compositions suitable carriers further include cell culture media used for culturing the insect cells, and cell culture supernatants. As discussed herein, the expressed NA is preferably not purified or isolated from the expression systems and mixed with a suitable carrier to generate the inventive vaccines. Rather, the expressed NA, along with infected 25 insect cells, membrane particles, and recombinant baculovirus (and associated cell culture and supernatants) can be directly dispersed in a carrier system noted above for administration without purification. The amount included in the composition is an amount that provides a therapeutically effective amount of expressed NA. Methods are described herein for detecting the amount of NA expressed from a given expression system. 30 As used herein, a "therapeutically effective" amount refers to the amount that will elicit the biological or medical response of a tissue, system, or subject that is being sought by a researcher or clinician, and in particular elicit some desired protective effect as against the viral infection by priming or stimulating an immune response specific for one or more strains of influenza virus (and 9 CA 3064760 2019-12-12 preferably at least the target strain). One of skill in the art recognizes that an amount may be considered therapeutically "effective" even if the condition is not totally eradicated or prevented, but it or its symptoms and / or effects are improved or alleviated partially in the subject. In some embodiments, the composition will comprise at least about 1 μg total NA, preferably at least 5 μg 5 total NA, more preferably at least 10 μg total NA, more preferably at least 15 μg total NA, more preferably more preferably at least 20 μg total NA, and even more preferably about 25 μg per dose or more. As used here "total" NA clarifies that if two different subtypes of NA are included in the vaccine, the total amount of all subtypes of NA in the composition. Other ingredients may be included in the composition, such as adjuvants, other active IO agents, preservatives, buffering agents, salts, other pharmaceutically-acceptable ingredients. The term "adjuvant" is used herein to refer to substances that have immunopotentiating effects and are added to or co-formulated in the vaccine composition in order to enhance, elicit, and / or modulate the innate, humoral, and / or cell-mediated immune response against the vaccine components. Suitable adjuvants include: aluminum salts, such as aluminum hydroxide, aluminum phosphate, 15 alum (potassium aluminum sulfate), or mixed aluminum salts, peptides, oil or hydrocarbon emulsions, or any other adjuvant deemed suitable for human or animal use. In one or more embodiments, the baculoviral components of the expression system itself contributes an adjuvant effect. Antibiotics can also be used as part of vaccine production and may be present in small amounts in the vaccine, such as neomycin, polymyxin B, streptomycin and gentamicin. 20 Advantageously, the immunogenic compositions of the invention specifically generate in the subject anti-influenza antibodies against NA only. Anti-NA antibodies do not prevent virus uptake but rather prevent the newly formed virus from escaping the cell. This is an important distinction as our vaccine also generates infection immunity, i.e., it allows a permissive infection by influenza but controls clinical disease and observable symptoms by preventing virus spread. 25 Not only do we get immunity targeted at the antigen in the vaccine, we also stimulate cell mediated immunity by allowing the virus limited replication in the vaccinated subject. Further, maternal anti-HA antibodies are nearly universally present in young animals, such as pigs, and interfere with vaccination. In contrast, anti-NA antibodies are largely low or nonexistent in animals vaccinated with traditional vaccines or following infection. As anti-NA 30 antibodies are low in the animals, we can vaccinate young and growing animals using the immunogenic compositions and not have maternal antibody interference. Further, the immunogenic compositions rely on expression of full-length, wild-type / native, membrane-bound NA, which promotes a more robust immune response as compared to purified 10 CA 3064760 2019-12-12 or soluble versions ofNA that have been previously attempted. Again, the NA used in the present compositions is not processed or purified. Consequently, the NA is found integrated in the insect cell membranes and the budded baculovirus membranes in the culture supematants. Presentation of NA in these complex structures likely makes it more immunogenic (especially as displayed on 5 the baculovirus viral membrane). Measures of NA activity in the culture have shown that about half is in the cells and the other half is in the supernatant (presumably in the baculovirus membranes in the supernatant). Homologous and heterologous challenge studies demonstrate that crude baculovirus culture (Sf9 cells+ baculovirus + S:f90011 media) containing at least 25μg each ofNAl and NA2 10 yields protection to influenza virus. The primary measurement of protection is reduction in lung lesions. The secondary measurement of protection is reduction in influenza viral titer in the lung. Vaccination / challenge studies demonstrate the NA inhibiting antibody titers are a good correlate of protection. Vaccines formulated at a minimum of 25 μg total NA / dose yield NI titers >40, however, doses as low as IO μg total NA have been demonstrated to provide a protective immune 15 response. Thus, described herein are vaccination methods or methods of stimulating an immune response against influenza infection, so as to inhibit, reduce, or even prevent symptoms of infection. The methods generally involve administering the immunogenic compositions to a host animal susceptible to influenza in an effective amount. The composition can be delivered 20 intramuscularly, subcutaneously, intradermally, or intravenously using a needle and syringe, or a needleless injection device, as well as mucosally, such as intranasal administration. Advantageously, there have been no adverse injection site reactions observed in vaccinated subjects thus far. While stimulation of a protective immune response with a single dose is preferred, additional dosages can be administered, by the same or different route, to achieve the 25 desired prophylactic or therapeutic effect. The vaccine can also be administered using a prime and boost regime if deemed necessary. In some embodiments, the methods described herein are useful for eliciting an immune response against influenza infection, as described above. Advantageously, the compositions provide an immune response and heterologous protection against influenza. Ideally, the compositions include at least one NA subtype NA 1 and 30 at least one NA subtype NA2 to broaden its protection coverage. Such an "immune response" includes, for example, the production or activation of antibodies, B cells and / or the various T cells, directed specifically to NAI and / or NAZ. The immune response will be demonstrated by a lack of observable clinical symptoms, or reduction of clinical symptoms normally displayed by an 11 CA 3064760 2019-12-12 infected animal, faster recovery times from infection, reduced duration or amount of viral shedding, and the like. Accordingly, vaccinated animals will display resistance to new infection ( or observable signs of infection) or reduced severity of infection, as compared to unvaccinated animals. "Reducing" the incidence, severity, and / or duration of clinical symptoms and / or viral 5 shedding, means reducing the number of infected animals in a group, reducing or eliminating the number of animals exhibiting clinical signs of infection, or reducing the severity of any clinical signs that are present in the animals, in comparison to wild-type infection in unvaccinated animals. In some embodiments, the vaccine can be provided in unit dosage form in a suitable container. The term "unit dosage form" refers to a physically discrete unit suitable as a unitary IO dosage for human or animal use. Each unit dosage form may contain a predetermined amount of the vaccine (and / or other active agents) in the carrier calculated to produce the desired effect. In other embodiments, the vaccine can be provided separate from the carrier (e.g., in its own vial, ampule, sachet, or other suitable container) for on-site mixing before administration to a subject. A kit comprising the vaccine is also disclosed herein. The kit further comprises instructions for 15 administering the vaccine to a subject. The virus can be provided as part of a dosage unit, already dispersed in a pharmaceutically-acceptable carrier (e.g., along with culture media and / or adjuvant solution), or it can be provided separately from the carrier. The kit can further comprise instructions for preparing the virus for administration to a subject, including for example, instructions for dispersing the virus in a suitable carrier. 20 Using the methodology and technology described herein compositions can be developed that are effective against H 1 NI, H3N 1, HI N2, and H3N2 viruses in pigs, and can be considered "universal" vaccine candidates. In other species, NA subtypes can be sequenced and used to create compositions that provide protection against various HxN1 or HxN2 viruses. Specifically, avian influenza is typically H5N 1 or H5N2. Chickens or turkeys can be vaccinated with 25 BacNA1 / BacNA2 to generate an antibody response to H5Nl / H5N2 viruses. Canine influenza is typically H3N8 or H3N2 so could predict BacNA2 would protect against canine influenza. Likewise, humans are typically infected with HIN I or H3N2 and may benefit from the vaccination strategies described herein. As used herein, the term "vaccine" refers to an immunogenic composition capable of 30 eliciting partial or complete immunogenic protection against a disease or condition in the subject to which it has been administered. Although vaccines are generally considered prophylactic, the vaccines may be used for therapeutic treatment of a disease or a condition. Compositions according to the embodiments disclosed herein are useful in treating viral infection from influenza 12 CA 3064760 2019-12-12 in a subject (e.g., swine) and / or preventing or reducing clinical symptoms of infection. Such clinical symptoms include respiratory distress, fever, anorexia and lethargy. Thus, embodiments described herein have therapeutic and / or prophylactic uses, and in particular can be used for prophylactic treatment of a viral infection. In general, the compositions are administered 5 prophylactically, that is, before the subject demonstrates detectable clinical signs of an infection, such that the subject develops an adaptive immune response to infection by the virus. As such, the methods are useful for preventing the development of observable clinical symptoms from viral infection, and / or reducing the incidence or severity of clinical symptoms, and / or effects of the infection, and / or reducing the duration of the infection / symptoms / effects, and / or reducing the 10 amount and / or duration viral shedding / viremia, as compared with unvaccinated control animals. Thus, the composition may only partially prevent and / or lessen the extent of morbidity due to the viral infection (i.e., reduce the severity of the symptoms and / or effects of the infection, and / or reduce the duration of the infection / symptoms / effects), as compared with unvaccinated control animals. Yet, the composition is still considered to treat or "prevent" the target infection or 15 disease, even though it is not 100% effective. Additional advantages of the various embodiments of the invention will be apparent to those skilled in the art upon review of the disclosure herein and the working examples below. It will be appreciated that the various embodiments described herein are not necessarily mutually exclusive unless otherwise indicated herein. For example, a feature described or depicted in one 20 embodiment may also be included in other embodiments, but is not necessarily included. Thus, the present invention encompasses a variety of combinations and / or integrations of the specific embodiments described herein. As used herein, the phrase "and / or," when used in a list of two or more items, means that any one of the listed items can be employed by itself or any combination of two or more of the 25 listed items can be employed. For example, if a composition is described as containing or excluding components A, 8, and / or C, the composition can contain or exclude A alone; B alone; C alone; A and B in combination; A and C in combination; B and C in combination; or A, B, and C in combination. The present description also uses numerical ranges to quantify certain parameters relating 30 to various embodiments of the invention. It should be understood that when numerical ranges are provided, such ranges are to be construed as providing literal support for claim limitations that only recite the lower value of the range as well as claim limitations that only recite the upper value of the range. For example, a disclosed numerical range of about 10 to about 100 provides literal 13 CA 3064760 2019-12-12 support for a claim reciting "greater than about 10" (with no upper bounds) and a claim reciting "less than about l 00" (with no lower bounds). EXAMPLES 5 The following examples set forth methods in accordance with the invention. It is to be understood, however, that these examples are provided by way of illustration and nothing therein should be taken as a limitation upon the overall scope of the invention. Example 1: Construction of a baculovirus strains that expresses SIV NA subtype 1 10 (NAl) or subtype 2 (NA2) The synthetic NA genes were synthesized at Integrated DNA Technologies with the addition of BamHI sites immediately upstream and downstream of the gene sequence. The NA protein genes of A / swine / Iowa / A01782229 / 2016(H1Nl) (SEQ ID NO:l) and A / swine / Oklahoma / A01730659 / 2016(H1N2) (SEQ ID NO:3) were downloaded from Genbank 15 under accessions KYI 15564 and KU752376, respectively. The synthetic NA genes were then cloned into the BamHI site of E.coli pAcAB3 (AB Vector- Catalog Number B2). After transformation into E.coli, DHSa cells, ampicillin-resistant colonies were selected and expanded in overnight 2mL cultures of Luria-Bertani broth with I 00 μg / mL ampicillin. Following plasmid DNA isolation with a Qiagen miniprep kit, plasmids were 20 screened by restriction digestion to identify clones which contained NA 1 or NA2 genes in the proper orientation (pAcAB3-NA1 and pAcAB3-NA2, respectively) by restriction endonuclease digestion. The identified clones were further verified by DNA sequencing. Plasmid DNA (pAcAB3-NA1 and pAcAB3-NA2) along with Bsu36 / -linearized baculovirus vector DNA (ProEasy, AB Vector, Catalog Number AlO) were used to transfect Sf9 25 (Spodopterafrugiperda) insect cells to produce recombinant baculovirus encoding either the NAl (SEQ ID NO:2) or NA2 (SEQ ID NO:4) expression cassette. Transfection was performed in a 6- well plate with lx106 cells / well. For each transfection sample, plasmid DNA and Profectin Reagent (AB Vector, Catalog Number Tl 0) complexes were prepared in 12 x 75mm sterile tubes as follows: 30 Solution A: 45μ1 water+ 5.0 μl Profectin transfection reagent Solution B: 44μ1 water+ 0.1 μg plasmid (pAcAB3-NA1 or pAcAB3-NA2) + 5 μL linearized baculovirus DNA (ProEasy, AB Vector) Solution A and Solution B were combined and incubated for 20 minutes at 20°C + / - 5°C. 14 CA 3064760 2019-12-12 Then, 0.9 mL ofSF-900 II medium was added to each tube before adding the complexes into Sf9 cells. The DNA profectin complexes were transferred into Sf9 cells and incubated for 24 hrs in 27° + / - 1°C. Two mL of fresh cell culture medium was then added to each well. The transfected cells were incubated at 27°C for generation of recombinant baculovirus. 5 Recombinant baculoviruses produced from transfection of Sf9 cells are usually released into the medium at 4 to 5 days post-transfection. Once the cells appeared infected (cell enlargement, internal granular formation, cell detached from cell culture surface, cell degradation), the viruses were harvested from the cell culture medium by centrifugation at 500x g for 10 minutes to remove cells and large debris. The recombinant baculoviruses were called PO viral stock. 10 The P 1 viral stocks were amplified in Sf9 cells by inoculation of 0.5 mL of PO material to a T75 shaker flask of ~60% confluent Sf9 cells in 20 mL of Sf90011 media. Pl was harvested on day 4 post infection. Similarly, Pl harvests (lmL) were used to infect 2-T225 flasks of Sf9 cells (~60% confluency) in 100 mL of Sf90011. Passage 2 (p2) recombinant baculoviruses were harvested on day 4 post infection and aliquoted as the Master Seed Stock, identified as BacNA 1 15 P2 072817 and BacNA2 P2 072817. Example 2: Verification of NA activity in BacNAl and BacNA2 The mature influenza NA protein is a tetrameric protein composed of four identical subunits. Mature NA has sialidase activity, cleaving sialic acid moieties on glycoproteins. Only 20 mature, tetrameric protein has this enzymatic activity. To verify that the NAl and NA2 genes expressed in baculovirus are enzymatically active, NA activity assays were performed. NA activity is assayed using 2-o-(p-nitrophenyl)-a.-D-N-acetylneuraminic acid (NPNANA, SigmaAldrich Nl516). For NA activity determination, 50 μL of 0.3mM NP-NANA is combined with 50 μL of clarified culture supernatant and incubated in a flat-bottomed 96 well 25 plastic plate for 1 hour at 37°C before stopping the reaction with the addition of 100 μL of 1.0 N NaOH and measuring absorbance at 405 nm. As shown in FIG. l, NA activity is confirmed by an absorbance >0.4 while supernatant from a control baculovirus culture has an absorbance <0.2. The control baculovirus culture is generated by culturing the baculovirus control strain, BacCon, under similar conditions. BacCon was constructed as described for Bae-NA 1 and Bac-NA2 except 30 pAcAB3 was used for transfection of Sf9 cells. BacCon does not contain a NA gene and establishes the background absorbance for baculovirus propagated in Sf9 cells. Example 3: Protection afforded pigs vaccinated with BacNAl to a heterologous H1N1 15 CA 3064760 2019-12-12 challenge. The experimental vaccine consisted of a crude mixture of Sf9 cells infected with the BacNAl and culture supernatant inactivated with binary ethyleneimine formulated with 15% commercial oil-in-water adjuvant (CASO, Cambridge Technologies). Groups of eight, influenza 5 seronegative three-week old pigs, acquired from Midwest Research Swine, were vaccinated with either inactivated BacNAl culture fluids, an inactivated whole-virus HIN2 SIV or mock vaccinated. Vaccines were administered intramuscularly at four and six weeks of age. Pigs were challenged intranasally with 2mL of 6.0 TCIDso / mL of a heterologous SIV A / swine / Minnesota / 2073 / 2008 (HINI). The challenge virus (a cluster) was heterologous both to 10 the inactivated H1N2 vaccine group (y cluster) as well as the recombinant NAl (92% similarity). Sera collected on the day of challenge was analyzed for a-IAV-S nucleoprotein antibodies using the commercially-available IDEXX ELISA assay. The IDEXX IAV-S NP ELISA and NA inhibition titers in sera collected from pigs on the day of challenge are shown in FIG. 2. All pigs inoculated with BacNA I or mock vaccinated remained negative while pigs vaccinated with an 15 inactivated H 1N2 vims were positive (FIG. 2). Sera were also analyzed for NA inhibiting antibody titers using the challenge virus. Pigs vaccinated with BacNAl had a mean NI titer of 69 while pigs in the other treatment groups were negative (FIG. 2). Nasal swabs were collected on the day of challenge and on days 1, 3 and 5 post-challenge. We employed two complementary approaches to detect viral shedding. The first approach was the 20 standard qRT-PCR with the Cycle threshold (Ct) values as the readout, which are shown in FIG. 3 for Ct values in nasal swabs collected from pigs on days 1, 3 and 5 post-challenge. It is generally agreed that the higher Ct values, the lower amount of viral load. The second approach was cellbased TCIDso experiment that measures the amount of infectious virus particles in nasal swabs. We used swine testicle (ST) cells for determining viral TCIDso. All pigs were negative for SIV on 25 the day of challenge by qRT-PCR. Interestingly, we found that our NI-based recombinant vaccine offered better protection than the inactivated H 1 N2 vaccine. Specifically, we observed that Cycle threshold (CT) values for pigs vaccinated for BacNA 1 were higher, representing lower levels of IAV-S shedding, on all three days (FIG. 3). FIG. 4 shows the SIV titers (TC1D50 / mL) in nasal swabs collected from pigs on days 1, 3 and 5 post challenge. Similar to the qRT-PCR results, 30 lower amounts of IAV-S were detected in BacNAI vaccinated pigs than pigs vaccinated with inactivated H1N2 virus or mock vaccinated (FIG. 4). On day 5 post challenge, pigs were euthanized and the lungs were removed in toto and scored by a blinded veterinarian based on gross lung consolidation in each lobe(%) which was 16 CA 3064760 2019-12-12 used to calculate total affected lung area. FIG. 5 shows the qRT-PCR Ct values and percent lung consolidation day 5 post challenge. Lung lesions were very low for BacNAl vaccinated pigs (0.34%) while considerable lung consolidation was observed both for H1N2 and mock vaccinated pigs (6.0 and 5.1%, respectively, FIG. 5). A portion of the right cardiac lung was also analyzed 5 for SIV by qRT-PCR. SIV was barely detectable for BacNAl vaccinated pigs (Ct=35.4) while high viral loads were detected in the H1N2 and mock treatment groups (Ct's 23.1 and 21.8, respectively). A portion of the right cardiac lobe was also fixed in formalin and analyzed for histopathology. Samples were scored on a 0-4 scale representing increased pathology based on 10 hematoxylin and eosin staining and immunohistochemistry for SIV. Microscopic lung lesion scores based on hematoxylin and eosin (H&E) staining and immunohistochemistry (IHC) for IA VS are shown in FIG. 6. The pathologist was blinded to the study design. Similar to the gross lung lesions, very little lung pathology was observed microscopically and SIV was not identified by IHC in BacNAl vaccinated pigs (FIG. 6). In contrast, significantly more lung lesions along with 15 associated IAV-S detection was observed in the HlN2 and mock treated pigs. Example 4: Protection afforded pigs vaccinated with BacNAl and BacNA2 to a heterologous H1N1 challenge. Baculovirus NI and N2 cultures (two separate strains) were concentrated lOx by 20 ultracentrifugation and used to formulate vaccines with straight antigen (0.85 mL NI lOx concentrate, 0.85mL N2 lOx concentrate, 0.3mL CASO adjuvant per dose) or I :5 and 1 :20 fold dilutions of the I Ox antigen concentrate. Pigs vaccinated at 3 and 5 weeks of age and challenged at 7 weeks of age with a heterologous HINl (6 TCIDso / mL) which has a Nl protein ~92% similar to BacNAl. 25 FIG. 7 shows the data from serology (NA inhibition assay) using parental HINl and H1N2 viruses as well as the challenge virus showing antibody generated to N l and N2. Serum was collected from all pigs on the day of challenge. The NI assay results show that both BacNA 1 and BacNA2 are able to stimulate an antibody response which is capable of inhibiting NAl and NA2 activity. Importantly, antibodies generated against BacNAl are able to cross react with the 30 heterologous virus used for challenge. FIG. 8 shows the results from PCR on lung tissue collected 5 days post challenge with heterologous HIN 1. These results show a dose-dependent effect such that influenza virus titers in the lungs post-challenge are inversely correlated with the amount of antigen used for vaccination. 17 CA 3064760 2019-12-12 Gross and microscopic lung scores on lungs collected 5 days post challenge are shown in FIG. 9. These results demonstrate that all three vaccines formulations were capable of providing protection to lung damage caused by influenza virus infection. As the antigen pool used to generate the three vaccines was 1 Ox concentrated baculovirus cultures, the vaccines represented 5 approximately 8.5, 1.7 and 0.43mL of BacNAl and BacNA2 per dose. Example S: Quantification of NA produced by BacNAl and BacNAl The full length native sequence of NAl and NA2 expressed by BacNAl and BacNA2, respectively, each contain an N-terminal transmembrane domain and consequently are found 10 associated with Sf9 cellular or baculovirus lipid membranes. Membrane proteins are difficult to purify. In order to generate highly purified reference standards for NA I and NA2 we expressed N-terminal truncated versions ofNAl (SEQ ID NO: 5) and NA2 (SEQ ID NO:6) in baculovirus which included the baculovirus GP67 secretion signal sequence to enable soluble protein expression. NA protein genes of A / swine / lowa / A01782229 / 2016(H1Nl) and 15 A / swine / Oklahoma / A0I 730659 / 2016 (HIN2) were synthesized such that the nucleotides encoding the N-terminal 35 amino acids were removed and replaced by the baculovirus Gp67 secretion signal peptide and a hexahistidine tag was added at the C-terminus of the protein (SEQ ID NO:5 and SEQ ID NO:6). The resulting genes were cloned into pAcAB3 and used to construct recombinant baculoviruses expressing soluble NAI and NA2 as described in Example 1. Sf9 cell 20 cultures of the resulting baculovirus strains were used to purify soluble NA 1 and NA2 from the culture supernatant using affinity chromatography (immobilized Ni2+). The purified NAl and NA2 proteins were visualized by SOS-PAGE and Western blotting using an antibody which recognizes the hexahistidine tag. The purity of NA in each preparation was determined by densitometry of the SOS-PAGE 25 gel to be >90%. In FIG. 10, Lane I contains 2 ug of bovine serum albumin standard as a reference. Lane 2 contains 2 ug of purified NA. Lane 3 contains 2 ug of purified NA.Protein concentration was determined by the Bradford assay using a bovine serum albumin standard curve. Purified NA I was 0.21 mg / mL and NA2 was 0.14 mg / mL. NA activity assays were performed on representative cultures of BacNAl and BacNA 1 30 along with purified, soluble NAI and NA2 as described in Example 2. Parallel line analysis was performed on the NA activity assay curves to determine the concentration of NA 1 and NA2 produced by BacNAI and BacNA2, respectively, using the purified reference NAl and NA2 of known concentration. Repeated measures of BacNA 1 and BacNA2 cultures found approximately 18 CA 3064760 2019-12-12 50 μg / mL NA in both cultures. Example 6. Protection afforded pigs vaccinated with BacNAl and BacNA2 to a homologous H1N2 challenge. 5 Baculovirus Nl and N2 cultures (two separate strains) were concentrated lOx by ultracentrifugation. The amount of NA present in the concentrated cultures were determined as described in Example 5. Vaccines were formulated to contain 200, 100, 50, 25 or O μg / dose of both NA I and NA2 and 15% CASO adjuvant. The dose volume was adjusted to 2 mL with phosphate buffered saline. Pigs were vaccinated at 3 and 5 weeks of age and challenged at 7 weeks 10 of age with the homologous HIN2 (6 TCID50 / mL) parental virus. Serology-NA inhibition antibody titer to parental viruses are shown in FIG. 11. All vaccine formulations induced antibody titers to both parental viruses. IA V PCR (Ct) values on nasal swabs collected on days 1, 2 and 5 post challenge and lung tissue collected day 5 post challenge are shown in FIG. 12. The amount of virus detected in nasal swabs and lungs were lower than mock 15 vaccinated pigs at all time points. FIG. 13 includes the gross and microscopic scores on lung tissue collected day 5 post challenge. All vaccine formulations significantly reduced lung lesions. Example 7. Protection afforded pigs vaccinated with BacNAl and BacNA2 to a homologous HlNl challenge. 20 Baculovirus NI and N2 cultures (two separate strains) were concentrated lOx by ultracentrifugation. The amount of NA present in the concentrated cultures were determined as described in Example 5. Vaccines were formulated to contain 200, 100, 50, 25 or O μg / dose of both NAl and NA2 and 15% CASO adjuvant. The dose volume was adjusted to 2 mL with phosphate buffered saline. Pigs were vaccinated at 3 and 5 weeks of age and challenged at 7weeks 25 of age with the homologous H 1 NI (6 TC!D50 / mL) parental virus. Serology-NA inhibition antibody titer to parental viruses are shown in FIG. 14. All vaccine formulations induced antibody titers to both parental viruses. The IA V PCR (Ct) values on nasal swabs collected on days 3 and 5 post challenge and lung tissue collected day 5 post challenge are shown in FIG. 15. While the amount ofinfluenza detected in nasal swabs for vaccinated pigs was 30 not significantly different than mock vaccinated pigs, all vaccine groups had significantly lower levels of influenza in lung samples. FIG. 16 shows the lung lesion scores GMT (geometric mean titer) as assessed by H&E and IHC staining were significantly reduced in all vaccine groups as compared to mock vaccinated pigs. 19 CA 3064760 2019-12-12 20 Example 8. Dose titration studies Further, dose titration studies were carried out. Pigs were vaccinated with crude baculovirus culture fluids as described at various dilution levels. The results are shown in FIG. 17-19. The 1x composition was formulated with 42.5 μg of NA1 and 42.5 μg of NA2 per dose. For the most dilute vaccine, 5 μg of NA1 and 5 μg of NA2 were enough antigen to give protection. FIG. 17 is a graph of serology 5 using the NA inhibition assay. It clearly shows seroconversion for all vaccines and a successful dose response (decreasing antigen leading to lower NI titer). FIG. 18 shows the results of lung lesion scores for N1 and N2. FIG. 19 shows lung lesion scores as assessed by H&E and IHC staining were significantly reduced in all vaccine groups as compared to mock vaccinated pigs. These results demonstrate that the crude baculovirus culture 10 fluids can be diluted ~8x and still be efficacious (~0.1mL BacNA1 / BacNA2 per dose). DISCUSSION The results from these vaccination trials convincingly demonstrate that immunity based on influenza NA-alone provides significant protection from homologous and heterologous challenge. While 15 NA-based immunity does not prevent infection, pigs were nearly completely protected from lung damage. Vaccination aimed at controlling viral dissemination in vivo may allow for the generation of infection immunity while mitigating clinical disease. Another exciting outcome of this study was the ability of recombinant NA1 to provide significant protection to a heterologous H1N1 challenge. To date, only SIVs containing two NA subtypes (N1 or N2) infect the global swine industry and 20 cause a significant economical concern. The NA genes of SIVs are less variable than the HA genes, which represents a good vaccine target. Currently FDA-approved inhibitors to treat human influenza are also targeting the functional NA protein. Including a HA component in the vaccines such as the marketed inactivated SIV vaccines will drive immune responses directed largely towards the immunodominant HA so antibody responses to NA with the universal protection potential will be masked or reduced. 25 In some aspects, embodiments of the present disclosure as described herein include the following items : 1. An immunogenic composition for use in inducing an immune response to influenza in an 30 animal, said composition comprising recombinant baculovirus expression vectors in cultured insect cells and a pharmaceutically acceptable carrier comprising insect cell culture media, said recombinant baculovirus expression vectors expressing a therapeutically effective amount of influenza neuraminidase, said neuraminidase being associated with the cell membrane of said insect cells and / or baculovirus viral membrane surfaces in said composition and presented on CA 3064760 Date reçue / Received date 2026-03-13 21 the surfaces of said membranes, wherein the composition is substantially free of influenza hemagglutinin HA, and wherein said animal is a swine, avian, canine, equine, or feline animal. 2. The immunogenic composition for use of item 1, wherein said recombinant baculovirus 5 expression vectors express: (a) the influenza neuraminidase, which is a native, full-length neuraminidase protein; or (b) the influenza neuraminidase obtained from the neuraminidase sequences of H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza 10 viruses. 3. The immunogenic composition for use of item 2, wherein said immune response comprises protecting said animal against H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses. 15 4. The immunogenic composition for use of any one of items 1 to 3, wherein said composition comprises a first set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 1 protein and a second set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 2 protein. 20 5. The immunogenic composition for use of item 4, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed to both the influenza neuraminidase subtype 1 protein and the influenza neuraminidase subtype 2 protein in said animal. 25 6. The immunogenic composition for use of item 1 or 2, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed specifically to the influenza neuraminidase in said animal. 30 7. The immunogenic composition for use of item 1 or 2, wherein said immune response comprises preventing influenza viral spread in said animal. CA 3064760 Date reçue / Received date 2026-03-13 22 8. The immunogenic composition for use of any one of items 1 to 7, wherein said composition further comprises an adjuvant. 9. The immunogenic composition for use of any one of items 1 to 8, wherein said composition is: (a) chemically 5 inactivated; (b) unpurified; (c) substantially free of one or more of the influenza proteins matrix proteins M1 or M2, RNA polymerase subunits PB1, PB2, and PA, nucleoprotein NP, and nonstructural proteins NS1 or NS2; or 10 (d) present in unit dosage form. 10. The immunogenic composition for use of any one of items 1 to 9, wherein said insect cells are Spodoptera frugiperda cells, Trichplusia ni cells, Bombyx mori cells, or a cell line obtained therefrom. 15 11. The immunogenic composition for use of any one of items 1 to 10, wherein said cell culture medium is serum free culture medium. 12. The immunogenic composition for use of any one of items 1 to 11, wherein the composition 20 is formulated for intramuscular, subcutaneous, intradermal, intravenous, or mucosal administration. 13. The immunogenic composition for use of any one of items 1 to 12, wherein said animal is susceptible to influenza. 25 14. The immunogenic composition for use of any one of items 1 to 13, wherein said animal is a young pig less than 8 weeks of age. 15. The immunogenic composition for use of any one of items 1 to 14, wherein said animal does 30 not comprise maternal antibodies that interfere with said immunogenic composition or immune response. CA 3064760 Date reçue / Received date 2026-03-13 23 16. Use of an immunogenic composition for inducing an immune response to influenza in an animal, said composition comprising recombinant baculovirus expression vectors in cultured insect cells and a pharmaceutically-acceptable carrier comprising insect cell culture media, said recombinant baculovirus expression vectors expressing a therapeutically effective amount of influenza neuraminidase, said neuraminidase being associated with the 5 cell membrane of said insect cells and / or baculovirus viral membrane surfaces in said composition and presented on the surfaces of said membranes, wherein the composition is substantially free of influenza hemagglutinin HA, and wherein said animal is a swine, avian, canine, equine, or feline animal. 10 17. Use of an immunogenic composition for the manufacture of a medicament for inducing an immune response to influenza in an animal, said composition comprising recombinant baculovirus expression vectors in cultured insect cells and a pharmaceutically-acceptable carrier comprising insect cell culture media, said recombinant baculovirus expression vectors expressing a therapeutically effective amount of influenza neuraminidase, said neuraminidase 15 being associated with the cell membrane of said insect cells and / or baculovirus viral membrane surfaces in said composition and presented on the surfaces of said membranes, wherein the composition is substantially free of influenza hemagglutinin HA, and wherein said animal is a swine, avian, canine, equine, or feline animal. 20 18. The use of item 16 or 17, wherein said recombinant baculovirus expression vectors express: (a) the influenza neuraminidase, which is a native, full-length neuraminidase protein; or (b) the influenza neuraminidase obtained from the neuraminidase sequences of H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses. 25 19. The use of item 18, wherein said immune response comprises protecting said animal against H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses. 20. The use of any one of items 16 to 19, wherein said composition comprises a first set of 30 recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 1 protein and a second set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 2 protein. CA 3064760 Date reçue / Received date 2026-03-13 24 21. The use of item 20, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed to both the influenza neuraminidase subtype 1 protein and the influenza neuraminidase subtype 2 protein in said animal. 5 22. The use of any one of items 16 to 18, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed specifically to the influenza neuraminidase in said animal. 23. The use of any one of items 16 to 18, wherein said immune response 10 comprises preventing influenza viral spread in said animal. 24. The use of any one of items 16 to 23, wherein the composition further comprises an adjuvant. 15 25. The use of any one of items 16 to 24, wherein said composition is: (a) chemically inactivated; (b) unpurified; (c) substantially free of one or more of the influenza proteins matrix proteins M1 or M2, RNA polymerase subunits PB1, PB2, and PA, nucleoprotein NP, and 20 nonstructural proteins NS1 or NS2; or (d) present in unit dosage form. 26. The use of any one of items 16 to 25, wherein said insect cells are Spodoptera frugiperda cells, Trichplusia ni cells, Bombyx mori cells, or a cell line obtained therefrom. 25 27. The use of any one of items 16 to 26, wherein said cell culture medium is serum free culture medium. 28. The use of any one of items 16 to 27, wherein the composition is formulated for 30 intramuscular, subcutaneous, intradermal, intravenous, or mucosal administration. 29. The use of any one of items 16 to 28, wherein said animal is susceptible to influenza. CA 3064760 Date reçue / Received date 2026-03-13 25 30. The use of any one of items 16 to 29, wherein said animal is a young pig less than 8 weeks of age. 31. The use of any one of items 16 to 30, wherein said animal does 5 not comprise maternal antibodies that interfere with said immunogenic composition or immune response. 32. A kit for use in inducing or stimulating an immune response against influenza infection in an animal, said kit comprising: 10 an immunogenic composition comprising recombinant baculovirus expression vectors in cultured insect cells and a pharmaceutically-acceptable carrier comprising insect cell culture media, said recombinant baculovirus expression vectors expressing a therapeutically effective amount of influenza neuraminidase, said neuraminidase being associated with the cell membrane of said insect cells and / or baculovirus viral membrane 15 surfaces in said composition and presented on the surfaces of said membranes, wherein the composition is substantially free of influenza hemagglutinin HA, and wherein said animal is a swine, avian, canine, equine, or feline animal; and instructions for administering said composition to said animal. 20 33. The kit for use of item 32, wherein said recombinant baculovirus expression vectors express: (a) the influenza neuraminidase, which is a native, full-length neuraminidase protein; or (b) the influenza neuraminidase obtained from the neuraminidase sequences of H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses. 25 34. The kit for use of item 33, wherein said immune response comprises protecting said animal against H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses. 35. The kit for use of any one of items 32 to 34, wherein said composition comprises a first set of 30 recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 1 protein and a second set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 2 protein. CA 3064760 Date reçue / Received date 2026-03-13 26 36. The kit for use of item 35, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed to both the influenza neuraminidase subtype 1 protein and the influenza neuraminidase subtype 2 protein in said animal. 5 37. The kit for use of item 32 or 33, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed specifically to the influenza neuraminidase in said animal. 38. The kit for use of item 32 or 33, wherein said immune response comprises 10 preventing influenza viral spread in said animal. 39. The kit for use of any one of items 32 to 38, wherein the composition further comprises an adjuvant. 15 40. The kit for use of any one of items 32 to 39, wherein said composition is: (a) chemically inactivated; (b) unpurified; (c) substantially free of one or more of the influenza proteins matrix proteins M1 20 or M2, RNA polymerase subunits PB1, PB2, and PA, nucleoprotein NP, and nonstructural proteins NS1 or NS2; or (d) present in unit dosage form. 41. The kit for use of any one of items 32 to 40, wherein said insect cells are Spodoptera frugiperda 25 cells, Trichplusia ni cells, Bombyx mori cells, or a cell line obtained therefrom. 42. The kit for use of any one of items 32 to 41, wherein said cell culture medium is serum free culture medium. 30 43. The kit for use of any one of items 32 to 42, wherein the composition is formulated for intramuscular, subcutaneous, intradermal, intravenous, or mucosal administration. CA 3064760 Date reçue / Received date 2026-03-13 27 44. The kit for use of any one of items 32 to 43, wherein said animal is susceptible to influenza. 45. The kit for use of any one of items 32 to 44, wherein said animal is a young pig less than 8 weeks of age. 5 46. The kit for use of any one of items 32 to 45, wherein said animal does not comprise maternal antibodies that interfere with said immunogenic composition or immune response. 10 CA 3064760 Date reçue / Received date 2026-03-13

Claims

28 CLAIMS:

1. An immunogenic composition for use in inducing an immune response to influenza in an animal, said composition comprising recombinant baculovirus expression vectors in cultured insect cells and a pharmaceutically acceptable carrier comprising insect cell culture media, said recombinant baculovirus expression vectors expressing a therapeutically effective amount of influenza neuraminidase, said neuraminidase being associated with the cell membrane of said insect cells and / or baculovirus viral membrane surfaces in said composition and presented on the surfaces of said membranes, wherein the composition is substantially free of influenza hemagglutinin HA, and wherein said animal is a swine, avian, canine, equine, or feline animal.

2. The immunogenic composition for use of claim 1, wherein said recombinant baculovirus expression vectors express: (a) the influenza neuraminidase, which is a native, full-length neuraminidase protein; or (b) the influenza neuraminidase obtained from the neuraminidase sequences of H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses.

3. The immunogenic composition for use of claim 2, wherein said immune response comprises protecting said animal against H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses.

4. The immunogenic composition for use of any one of claims 1 to 3, wherein said composition comprises a first set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 1 protein and a second set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 2 protein.

5. The immunogenic composition for use of claim 4, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed to both the influenza neuraminidase subtype 1 protein and the influenza neuraminidase subtype 2 protein in said animal. CA 3064760 Date reçue / Received date 2026-03-13 29 6. The immunogenic composition for use of claim 1 or 2, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed specifically to the influenza neuraminidase in said animal.

7. The immunogenic composition for use of claim 1 or 2, wherein said immune response comprises preventing influenza viral spread in said animal.

8. The immunogenic composition for use of any one of claims 1 to 7, wherein said composition further comprises an adjuvant.

9. The immunogenic composition for use of any one of claims 1 to 8, wherein said composition is: (a) chemically inactivated; (b) unpurified; (c) substantially free of one or more of the influenza proteins matrix proteins M1 or M2, RNA polymerase subunits PB1, PB2, and PA, nucleoprotein NP, and nonstructural proteins NS1 or NS2; or (d) present in unit dosage form.

10. The immunogenic composition for use of any one of claims 1 to 9, wherein said insect cells are Spodoptera frugiperda cells, Trichplusia ni cells, Bombyx mori cells, or a cell line obtained therefrom.

11. The immunogenic composition for use of any one of claims 1 to 10, wherein said cell culture medium is serum free culture medium.

12. The immunogenic composition for use of any one of claims 1 to 11, wherein the composition is formulated for intramuscular, subcutaneous, intradermal, intravenous, or mucosal administration.

13. The immunogenic composition for use of any one of claims 1 to 12, wherein said animal is susceptible to influenza. CA 3064760 Date reçue / Received date 2026-03-13 30 14. The immunogenic composition for use of any one of claims 1 to 13, wherein said animal is a young pig less than 8 weeks of age.

15. The immunogenic composition for use of any one of claims 1 to 14, wherein said animal does not comprise maternal antibodies that interfere with said immunogenic composition or immune response.

16. Use of an immunogenic composition for inducing an immune response to influenza in an animal, said composition comprising recombinant baculovirus expression vectors in cultured insect cells and a pharmaceutically-acceptable carrier comprising insect cell culture media, said recombinant baculovirus expression vectors expressing a therapeutically effective amount of influenza neuraminidase, said neuraminidase being associated with the cell membrane of said insect cells and / or baculovirus viral membrane surfaces in said composition and presented on the surfaces of said membranes, wherein the composition is substantially free of influenza hemagglutinin HA, and wherein said animal is a swine, avian, canine, equine, or feline animal.

17. Use of an immunogenic composition for the manufacture of a medicament for inducing an immune response to influenza in an animal, said composition comprising recombinant baculovirus expression vectors in cultured insect cells and a pharmaceutically-acceptable carrier comprising insect cell culture media, said recombinant baculovirus expression vectors expressing a therapeutically effective amount of influenza neuraminidase, said neuraminidase being associated with the cell membrane of said insect cells and / or baculovirus viral membrane surfaces in said composition and presented on the surfaces of said membranes, wherein the composition is substantially free of influenza hemagglutinin HA, and wherein said animal is a swine, avian, canine, equine, or feline animal.

18. The use of claim 16 or 17, wherein said recombinant baculovirus expression vectors express: (a) the influenza neuraminidase, which is a native, full-length neuraminidase protein; or (b) the influenza neuraminidase obtained from the neuraminidase sequences of H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses. CA 3064760 Date reçue / Received date 2026-03-13 31 19. The use of claim 18, wherein said immune response comprises protecting said animal against H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses.

20. The use of any one of claims 16 to 19, wherein said composition comprises a first set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 1 protein and a second set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 2 protein.

21. The use of claim 20, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed to both the influenza neuraminidase subtype 1 protein and the influenza neuraminidase subtype 2 protein in said animal.

22. The use of any one of claims 16 to 18, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed specifically to the influenza neuraminidase in said animal.

23. The use of any one of claims 16 to 18, wherein said immune response comprises preventing influenza viral spread in said animal.

24. The use of any one of claims 16 to 23, wherein the composition further comprises an adjuvant.

25. The use of any one of claims 16 to 24, wherein said composition is: (a) chemically inactivated; (b) unpurified; (c) substantially free of one or more of the influenza proteins matrix proteins M1 or M2, RNA polymerase subunits PB1, PB2, and PA, nucleoprotein NP, and nonstructural proteins NS1 or NS2; or (d) present in unit dosage form.

26. The use of any one of claims 16 to 25, wherein said insect cells are Spodoptera frugiperda cells, Trichplusia ni cells, Bombyx mori cells, or a cell line obtained therefrom. CA 3064760 Date reçue / Received date 2026-03-13 32 27. The use of any one of claims 16 to 26, wherein said cell culture medium is serum free culture medium.

28. The use of any one of claims 16 to 27, wherein the composition is formulated for intramuscular, subcutaneous, intradermal, intravenous, or mucosal administration.

29. The use of any one of claims 16 to 28, wherein said animal is susceptible to influenza.

30. The use of any one of claims 16 to 29, wherein said animal is a young pig less than 8 weeks of age.

31. The use of any one of claims 16 to 30, wherein said animal does not comprise maternal antibodies that interfere with said immunogenic composition or immune response.

32. A kit for use in inducing or stimulating an immune response against influenza infection in an animal, said kit comprising: an immunogenic composition comprising recombinant baculovirus expression vectors in cultured insect cells and a pharmaceutically-acceptable carrier comprising insect cell culture media, said recombinant baculovirus expression vectors expressing a therapeutically effective amount of influenza neuraminidase, said neuraminidase being associated with the cell membrane of said insect cells and / or baculovirus viral membrane surfaces in said composition and presented on the surfaces of said membranes, wherein the composition is substantially free of influenza hemagglutinin HA, and wherein said animal is a swine, avian, canine, equine, or feline animal; and instructions for administering said composition to said animal.

33. The kit for use of claim 32, wherein said recombinant baculovirus expression vectors express: (a) the influenza neuraminidase, which is a native, full-length neuraminidase protein; or (b) the influenza neuraminidase obtained from the neuraminidase sequences of H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses. CA 3064760 Date reçue / Received date 2026-03-13 33 34. The kit for use of claim 33, wherein said immune response comprises protecting said animal against H1N1, H3N1, H1N2, H3N2, H5N1, H5N2, H3N8, and / or H3N2 influenza viruses.

35. The kit for use of any one of claims 32 to 34, wherein said composition comprises a first set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 1 protein and a second set of recombinant baculovirus expression vectors expressing the influenza neuraminidase subtype 2 protein.

36. The kit for use of claim 35, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed to both the influenza neuraminidase subtype 1 protein and the influenza neuraminidase subtype 2 protein in said animal.

37. The kit for use of claim 32 or 33, wherein said immune response comprises production or activation of antibodies, B cells and / or T cells, directed specifically to the influenza neuraminidase in said animal.

38. The kit for use of claim 32 or 33, wherein said immune response comprises preventing influenza viral spread in said animal.

39. The kit for use of any one of claims 32 to 38, wherein the composition further comprises an adjuvant.

40. The kit for use of any one of claims 32 to 39, wherein said composition is: (a) chemically inactivated; (b) unpurified; (c) substantially free of one or more of the influenza proteins matrix proteins M1 or M2, RNA polymerase subunits PB1, PB2, and PA, nucleoprotein NP, and nonstructural proteins NS1 or NS2; or (d) present in unit dosage form.

41. The kit for use of any one of claims 32 to 40, wherein said insect cells are Spodoptera frugiperda cells, Trichplusia ni cells, Bombyx mori cells, or a cell line obtained therefrom. CA 3064760 Date reçue / Received date 2026-03-13 34 42. The kit for use of any one of claims 32 to 41, wherein said cell culture medium is serum free culture medium.

43. The kit for use of any one of claims 32 to 42, wherein the composition is formulated for intramuscular, subcutaneous, intradermal, intravenous, or mucosal administration.

44. The kit for use of any one of claims 32 to 43, wherein said animal is susceptible to influenza.

45. The kit for use of any one of claims 32 to 44, wherein said animal is a young pig less than 8 weeks of age.

46. The kit for use of any one of claims 32 to 45, wherein said animal does not comprise maternal antibodies that interfere with said immunogenic composition or immune response. CA 3064760 Date reçue / Received date 2026-03-13