Next-Generation Computationally Designed Influenza Hemagglutinin Vaccines Protect against H5Nx Virus Infections

H5N1 COBRA hemagglutinin (HA) sequences, termed human COBRA-2 HA, were constructed through layering of HA sequences from viruses isolated from humans collected between 2004–2007 using only clade 2 strains. These COBRA HA proteins, when expressed on the surface of virus-like particles (VLP), elicited protective immune responses in mice, ferrets, and non-human primates. However, these vaccines were not as effective at inducing neutralizing antibodies against newly circulating viruses. Therefore, COBRA HA-based vaccines were updated in order to elicit protective antibodies against the current circulating clades of H5Nx viruses. Next-generation COBRA HA vaccines were designed to encompass the newly emerging viruses circulating in wild avian populations. HA amino acid sequences from avian and human H5 influenza viruses isolated between 2011–2017 were downloaded from the GISAID (Global Initiative on Sharing All Influenza Data). Mice were vaccinated with H5 COBRA rHA that elicited antibodies with hemagglutinin inhibition (HAI) activity against H5Nx viruses from five clades. The H5 COBRA rHA vaccine, termed IAN8, elicited protective immune responses against mice challenged with A/Sichuan/26621/2014 and A/Vietnam/1203/2004. This vaccine elicited antibodies with HAI activity against viruses from clades 2.2, 2.3.2.1, 2.3.4.2, 2.2.1 and 2.2.2. Lungs from vaccinated mice had decreased viral titers and the levels of cellular infiltration in mice vaccinated with IAN-8 rHA were similar to mice vaccinated with wild-type HA comparator vaccines or mock vaccinated controls. Overall, these next-generation H5 COBRA HA vaccines elicited protective antibodies against both historical H5Nx influenza viruses, as well as currently circulating clades of H5N1, H5N6, and H5N8 influenza viruses.


Introduction
The H5 highly pathogenic avian influenza viruses from the genetic clade 2.3.4.4 emerged in China in 2010-2011. These viruses were detected in birds in more than 24 countries in the eastern hemisphere [1]. As of February 2020, the World Health Organization (WHO) reported 24 cases of human infections [2] by viruses of the H5N6 subtype, which is the only 2.3.4.4 clade H5 influenza virus that has infected people [3]. The newest cases of H5N6 virus infections in humans both occurred in China in September 2017 and recent infections in people with viruses that had HA proteins that were phylogenetically distinct from one another [4]. In 2014, H5N8 Eurasian subtypes was detected in U.S. Washington state in captive falcons, wild birds, and poultry [5,6]. These viruses spread across the central regions of North America devastating the poultry industry [6]. The clade 2.3.4.4 viruses from Africa and Europe were primarily of the H5N8 subtype, whereas those viruses isolated in Asia are in the H5N6 subtype and those strains isolated in the United States are classified as H5N2 isolates [4]. Clade 2.3.4.4 H5Nx viruses isolated from Africa and Europe are primarily of the H5N8 subtypes and those found in Asia are H5N6 subtype [1]. The H5N8 viral subtype caused an outbreak in 2014 in South Korea leading to a distinction can reassort with NA gene segments that are naturally found in avian species and have an increasing tendency towards binding to sialic acid receptors more commonly found in the upper respiratory tract of humans. These features of the H5Nx viruses have further increased the potential of these viruses to cross over into the human population. Along with reassortant events, the HA mutational rate is also problematic, as observed by the phylogenetic branching and lack of HAI titers against reference strains. In the last two years, two major viral clades have been circulating in the wild waterfowl populations, clade 2.3.4.4 and 2.3.2.1. [2] Mandatory vaccination of poultry was established in Guangdong province in China using an inactivated influenza virus vaccine [18]. This vaccine regimen decreased the prevalence of H7N9 influenza virus circulation in live poultry markets, however, circulation of H5N6 viruses continued and increased in antigenic diversity compared to the vaccine strain [18]. In 2018, the Chinese Government and the WHO approved a new A/Guangdong/18F020/2018 candidate vaccine virus [18]. However, vaccine escape mutants are still a risk for the animal and human populations. Reference sera generated by the WHO revealed that reference antigens A/Sichuan/26221/2014, A/Hubei/29578/2016 and A/Fujian-Sanyuan/21099/2017 do not generate antibodies against the A/Guangdong/ 18SF020/2018 vaccine strain [19].
Although  [21]. These compounding factors further exacerbate the need for a pandemic vaccine for both domestic poultry and the at-risk human population that spans multiple viral H5Nx clades.

Next-Generation Computationally Optimized Broadly Reactive Antigens (COBRA) Design
Next generation computationally optimized broadly reactive antigens (COBRA) H5 HA antigen were generated through a consensus sequence alignment of H5NX HA sequences from human and avian isolates. Sequences were downloaded through the GISAID database based on area, date of submission and the species of isolation. These sequences were then organized and used to generate multiple consensus sequences in order to capture the repeated and unique H5 epitopes. The COBRA approach used 10-20 primary consensus sequences isolated over a 4-5 year time frame using the sequences taken from 2011-2015, 2012-2016, 2013-2017) and one 5-year-long span (2011-2016). The HA sequence was downloaded into Geneious (San Diego, CA, USA) and aligned using Muscle alignment. The HA1 fragment of each HA sequence was extracted to produce the unique HA sequences. The AAs 17-340 were extracted and were then imported into a new file for re-alignment. The remaining 322 AA were used to create the COBRA HA1 sequence (Supplementary Figure S1). These sequences were used to generate a phylogenetic tree ( Figure 1) and were then condensed based upon identity and on the tree. Sequences that were condensed had no more that 2.5% difference and no ambiguities (X amino acid). Each primary sequence was labeled to represent the original sequences that were used in each primary consensus sequence. These primary consensus sequences were further combined into another phylogenetic tree and were combined to create unique sequences with no ambiguities. Over 50 sequences were generated using this method, but only eight were chosen due to their unique AA sequence and their placement on the phylogenetic tree. Sequences that were clustered too closely together with wild-type sequences and were not found to be closely associated with the root were ruled out. Each segment was blasted to confirm its uniqueness. The leader sequences (first 17 AA) were taken from a wild-type Sequences that were clustered too closely together with wild-type sequences and were not found to be closely associated with the root were ruled out. Each segment was blasted to confirm its uniqueness. The leader sequences (first 17 AA) were taken from a wild-type virus that was closely related to the unique COBRA virus. This was done to ensure the sequence would be properly localized in the cell. The final 8 sequences were generated by Genewiz (South Plainfield, NJ, USA) into out acceptor vector plasmid Zeo+ pcDNA3.1 (Thermo Fisher Scientific, Waltham, MA, USA).

Recombinant Protein Production
Each wild-type and COBRA recombinant HA protein was purified as described as in Ecker et al. (2020). Briefly, the HA gene cassettes expressing wild-type or COBRA HA recombinant protein from the H5NX subtype were cloned into mammalian DNA expression plasmid pcDNA 3.1/Zeo(+)vector (Thermo Fisher Scientific) and were synthesized by Genewiz (South Plainfield NJ, USA). The plasmid was transformed into the Top 10 bacterial cell line and was purified using Zympure maxi-prep. The HA1 fragment, which contained a KPNI site was removed from the plasmid and was moved into an acceptor vector containing the Hu-CO2 HA2 domain. The final gene of the HA protein contained an extracellular domain that was terminally fused with the trimeric domain of T4 fibritin, an

Recombinant Protein Production
Each wild-type and COBRA recombinant HA protein was purified as described as in Ecker et al. (2020). Briefly, the HA gene cassettes expressing wild-type or COBRA HA recombinant protein from the H5NX subtype were cloned into mammalian DNA expression plasmid pcDNA 3.1/Zeo(+)vector (Thermo Fisher Scientific) and were synthesized by Genewiz (South Plainfield, NJ, USA). The plasmid was transformed into the Top 10 bacterial cell line and was purified using Zympure maxi-prep. The HA1 fragment, which contained a KPNI site was removed from the plasmid and was moved into an acceptor vector containing the Hu-CO2 HA2 domain. The final gene of the HA protein contained an extracellular domain that was terminally fused with the trimeric domain of T4 fibritin, an AviTag sequence and a hexahistidine affinity tag for purification [22]. Each DNA plasmid containing either wild-type or COBRA antigens were transiently transfected into Expi293F HEK suspension cell line (Thermo Fisher Scientific) and was allowed to incubate for 72 h at 37 • C (5% CO2). Supernatants were collected and were tested for protein expression through BCA and Western blot (His tag antibody). The cells were then pelleted down and the supernatant was purified for protein collection. Soluble HA protein was purified via AKTA Pure System using HisTrap columns following the manufacturers protocol. Eluted fractions were pooled and purified, protein concentration was tested though anti-HIS tag antibody (Biolegend, San Diego, CA, USA) using SDS-PAGE and Western blot [23].

Viruses
Viruses were obtained through the Influenza Reagents Resource (IRR) and passaged once in embryonated chicken eggs as per the instructions provided by the WHO [24]. Virus lots were tittered with horse erythrocytes and made into aliquots for single-use applications. The H5NX vaccine panel includes the following reassortant PR8

Mouse Studies
BALB/c mice (female, 6-to 8-weeks-old) were purchased from The Jackson Laboratory (Bar Harbor, ME, USA) and were housed in microisolator units and fed ad libitum. Mice were handled in accordance with UGA IACUC protocols and were cared for under the U.S. Department of Agriculture guidelines for laboratory animals. Mice were humanely euthanized in case of weight loss ≥25% of the original weight. After the mice were acclimated for 7 days, they were bled to ensure all were immune naïve prior to vaccination. After naïve mice were confirmed, mice were vaccinated using 5 µg of recombinant protein formulated with an oil-in-water nano-emulsion adjuvant AddaVax™ according to the manufacturer's protocols. Mice were vaccinated three times at a 4-week interval to obtain appropriate antibody response (n = 10). Four weeks following the last vaccination, mice were intranasally infected with 2 × 10 7 pfu of recombinant A/Sichuan/26621/2014 virus and 1 × 10 7 pfu of A/Vietnam/1203/2004-PR8 reassortant virus. Mice were briefly anesthetized in an isoflurane chamber and were intranasally inoculated with 50µL of virus. The mice were allowed to recover and were monitored 2× daily for weight loss, clinical signs and mortality for up to 14 days.

Hematoxylin and Eosin (H&E) Staining
To assess the viral replication and pathological effect of infection, mice (n = 3) were euthanized 3 days post infection. The right lung lobes were taken for viral plaques and the incision was clamped with a hemostat, a 22 gauge needle was then used to puncture the apex of the heart and sterile PBS was perfused throughout the mouse for 2-3 min. After the blood was efficiently removed from the lungs, 10% formalin was then perfused to fix the left lobes. Lungs were removed and placed into formalin for 1 week prior to paraffin embedding. Mouse lungs were embedded in paraffin and were cut using a Lecia microtome. Transverse 5 µm sections were placed onto Apex superior adhesive glass slides (Leica biosystem Inc., Lincolnshire, IL, USA) which were coated for a positive charge. and were processed for H&E staining. Sections were deparaffinized in xylene and hydrated using different concentrations of ethanol (100%, 95%, 80% and 75%) for 2 min each. Deparaffinized and hydrated lung sections are stained with hematoxylin (Millipore sigma, Burlington, MA, USA) for 8 min at RT, differentiated in 1% acid alcohol for 10 s, and then counterstained with eosin (Millipore sigma, Burlington, MA, USA) for 30 s, slides were dehydrated with 95% and 100% ethanol, cleared by Xylene, and mounted using Permount ® mounting media (Thermo Fisher scientific, Waltham, MA, USA).

Immunohistochemistry Staining
The deparaffinized and hydrated lung tissue sections were subjected to antigen retrieval by sub-boiling in 10 nm sodium citrate buffer at pH = 6 for 10 min and then incubated in 3% fresh made hydrogen peroxide for 10 min to inactivate endogenous peroxidase at room temperature. The lung sections were blocked with 5% horse serum in PBS, incubated with mouse Influenza A Nucleoprotein monoclonal antibody at 1:1000 dilution (Bio-Rad, Hercules, CA, USA) overnight at 4 • C, and then incubated with biotinylated goatantibody mouse IgG H&L (Abcam, Burlington, MA, USA) at 1:2000 dilution for 1 h at RT. The avidin-biotin-peroxidase complex (VectStain Standard ABC kit) (Vector Laboratories, Burlingame, CA, USA) was used to localize the biotinylated antibody, and DAB (Vector Laboratories, Burlingame, CA, USA) was utilized for color development. Sections were then counterstained with hematoxylin, and then mounted using Permount ® mounting media (Thermo Fisher scientific, Waltham, MA, USA). Images were obtained by Aperio digital slide scanner AT2 (Leica biosystem, Lincolnshire, IL, USA).

Plaque Assays
Viral titers were determined in BALB/c mice using a plaque-forming assay as previously described [25][26][27][28][29] using 1 × 10 6 Madin-Darby Canine Kidney (MDCK) cells. Mice were euthanized (n = 3/group) 3 days post-infection, lungs were taken and snapped frozen and kept at −80 • C until processing. Lungs were diluted (10 0 to 10 6 ) and overlaid onto confluent MDCK cell layers for 1 h in 200 µL of DMEM supplemented with penicillinstreptomycin. Cells were washed after 1-h incubation and DMEM was replaced with 4 mL of L15 and 2.4% Avicel (FMC BioPolymer; Philadelphia, PA, USA) (1:1). Cells were incubated for 72 h at 37 • C with 5% CO 2 . Avicel and L15 media was removed and the samples were washed twice with sterile PBS, then cells were fixed with 10% buffered formalin and stained for 15 min with 1% crystal violet. Cells were washed with tap water and allowed to dry. Plaques were counted and the plaque forming units calculated (PFU/mL)

Hemagglutination-Inhibition (HAI) Assay
The hemagglutinin-inhibition assay (HAI) assay was used to assess receptor-blocking antibodies to the HA protein to inhibit agglutination of horse erythrocytes. The protocol was taken from the CDC laboratory influenza surveillance manual. To inactivate nonspecific inhibitors, mouse sera was treated with receptor destroying enzyme (RDE, Denka Seiken, Co., Tokyo, Japan) prior to being tested. Three parts of RDE were added to one-part sera and incubated overnight at 37 • C. The RDE was inactivated in 56 • C for 30 min and, when cooled, six parts of sterile PBS was added to the sera and was kept at 4 • C until use. RDE-treated serum was two-fold serially diluted in v-bottom microtiter plates. 25 µL of virus at 8 HAU/50 µL was added to each well (4 HAU per 25 µL). Plates were covered and incubated with virus for 20 min at room temperature before adding 1% horse red blood cells (HRBC) (Lampire Biologicals, Pipersville, PA, USA) in PBS. Red blood cells were washed and stored at 4 • C and used within a week of preparation. The plates were mixed by agitation and covered, and the RBCs were allowed to settle for 1 h at room temperature. HAI titer was determined by the reciprocal dilution of the last well which contained non-agglutinated RBC. Negative and positive serum controls were included for each plate. All mice were negative (HAI < 1:10) for pre-existing antibodies to currently circulating human influenza viruses prior to vaccination.

P-Epitope/P-Sequence Analysis
In order to assess the antigenic distances between the HA sequences used in the vaccines and the HA sequences used in the target strains, a P −sequence analysis was performed on the vaccine and virus strain and used to calculated antigenic distances. The epitopic value was calculated by the number of amino acid changes divided by the number of amino  Table S1). A multilayered consensus building approach was applied to 4524 A(H5Nx) HA amino acid sequences collected from 2011 to 2017, that resulted in the generation of eight unique next-generation HA sequences ( Table 1). All next-generation H5 HA amino acid sequences were unique and did not match the amino acid sequence of any HA in a wild-type A(H5Nx) isolate. Vaccines were phylogenetically spread across multiple viral clades (Table 1). Each wild-type and COBRA H5 HA protein was expressed in mammalian cell lines purified over a nickel column using the carboxyl-terminal 6× HIS-tag. These purified HA proteins were used as immunogens to vaccinate BALB/c mice (n = 8; 6-8 weeks of age) at day 1 and boosted at day 28. Along the 8 vaccines used, groups of mice were vaccinated with one of four wild-type rHA (WS/05, Sich/14, Gry/WA/14, ck/Egypt/17) (Figure 2). Mice were vaccinated with a traditional H5 COBRA HA antigen, Hu-CO 2, as a positive control and a mock vaccinated mice were used as a negative control. Sera collected at day 42 post-vaccination was tested for HAI activity against a panel of five viruses, WS/05 (2.

Vaccines Elicit Antibodies with Hemagglutination-Inhibition Activity
Mice vaccinated with wild-type HA antigens elicited antibodies with HAI activity against some, but not all, H5Nx viruses in the panel (Figure 2). The two HA vaccines based upon 2.3.4.4 viruses elicited antibodies with high HAI activity against the 2.3.4.4. viruses and Gz/13 (Figure 2A,B), but not the clade 2.2 based H5 viruses. In contrast, WS/05 HA vaccinated mice had antibodies with HAI activity against Hu/10 and WS/05 viruses ( Figure 2D) that were similar to the antibodies elicited by the traditional H-CO2 HA vaccine ( Figure 2E) [30].
Mice vaccinated with the next-generation H5 COBRA HA antigens elicited antibodies with HAI activity against different sets of H5Nx viruses (Figure 3). IAN-3 and IAN-6 HA vaccinated mice elicited antibodies that had similar HAI activity as antibodies elicited by the wild-type clade 2.3.4.4 HA proteins from Si/14 and gy/WA/14 ( Figure 3C,F). Mice vaccinated with IAN-2 HA did not elicit antibodies with HAI activity against any of the viruses in the panel ( Figure 3B). Overall, only three out of the eight next generation H5 HA vaccines, IAN-4, IAN-7 and IAN-8 HA vaccines elicited antibodies with HAI activity against H5 viruses in all four clades. All mock vaccinated mice were serologically negative to the viruses in the panel.

Viral Challenge
Mice were challenged with either VN/04 or Si/14 at day 56 post-vaccination ( Figure 5). Mice lost~75% of their body weight by day 7 post-infection, regardless of the virus used for infection. All vaccinated mice infected with SI/14 survived challenge ( Figure 5C), and mice vaccinated with the SI/14 or gry/WA/14 HA maintained the same average weight for the 10 days of observation. Mice vaccinated with IAN-7 HA actually gained weight following the challenge ( Figure 4A). Mice vaccinated with the other COBRA HA or wild-type HA antigens lost between 7-10% body weight by day 3 and then recovered to full body weight by day 10 post-infection. In contrast, only one mouse vaccinated with IAN-7 HA survived VN/04 challenge ( Figure 4D). Seventy percent of mice vaccinated with SI/14, gry/WA/14 or IAN-4 HA survived challenge with VN/04, but they lost an average 10-12% of their original body weight by day 5 post-infection. This weight loss was statistically the same as mice vaccinated with VN/04, IAN8, or Hu-CO-2 HA vaccinated mice ( Figure 4B), which all survived VN/04 challenge ( Figure 4D). Mock vaccinated mice had~5 × 10 3 pfu lung viral titers regardless which of the two H5Nx viruses was used for challenge ( Figure 6). All vaccinated mice had no SI/14 virus detectable in lung tissue at day 3 post-infection ( Figure 6B). In contrast, mice vaccinated with VN/04 or IAN-8 HA vaccines had an average of 10 pfu viral lungs titers collected 3 days post-infection with VN/04 virus ( Figure 6A). Mice vaccinated with the other 4 HA vaccines had low to moderate lung viral titers (50-200 pfu) from lungs collected day 3 post-infection with VN/04 ( Figure 6B). As expected, control mice that were not vaccinated had the highest titers compared to vaccinated mice. All vaccinated mice that were challenged with Si/14 had no viral lung titers. This was consistent with the lack of mortality in these groups.

Histopathology
Lungs collected on day 3 post-infection were analyzed for histopathology by H&E staining (Figures 7 and 8) and immunohistochemistry (IHC) (Figures 9 and 10) for detection of influenza virus NP nucleoprotein. Mice vaccinated with IAN-4, IAN-7, VN/04 HA and the mock control had the highest amounts of cellular infiltrates and inflammation ( Figure 7A,B,F,G) following Si/14 virus challenge. However, mice vaccinated with IAN-8 HA or the homologous Si/14 HA control had fewer stained infiltrating cells that were similar to the unchallenged mock control lungs ( Figure 7C,E,H). The amount of inflammation in the lungs of IAN-4 HA vaccinated mice correlated with the increased amounts of virus detected in these lungs ( Figure 7A). Mice challenged with VN/04 virus also had high levels of lung inflammation in IAN-4 HA vaccinated and in Si/14 HA vaccinated mice ( Figure 8A,E). Inflammation was inhibited in the lungs of mice that were vaccinated with either IAN-7, IAN-8, Hu-CO2 or VN/04 HA compared to the mock vaccinated control challenged lungs ( Figure 8B-D,F-G). VN/04 influenza virus infection induced less lung inflammation than Si/14 challenged mice.     Figure 10A,B,E,G). IAN-8 HA vaccinated mice had lungs with IHC staining levels that were similar to mock unchallenged lungs with low levels of viral NP staining ( Figure 9C,H). Lastly, the lungs of mice vaccinated with VN/04 HA vaccines had viral NP stained epithelial cells, but increased cellular infiltrates were consistent with a lack of NP binding.

Discussion
As part of universal vaccine development, next-generation influenza virus vaccines not only should protect against seasonal IAV and IBV antigenic drift, but also against the emergence of novel strains and subtypes not currently circulating in the human population. Therefore, one goal is to generate an influenza virus vaccine that efficiently protects against emerging pandemic virus subtypes with multiple antigenic variants, such as H5Nx strains. In this study, COBRA HA designed vaccines were evaluated in a mouse model by comparing the elicited immune responses and protective efficacy to wild-type H5 HA vaccines. Three next-generation vaccines, IAN-4, IAN-7 and IAN-8 HA, were as efficient as the original H5 COBRA HA, H-CO-2 [26], at eliciting broadly reactive immune responses. All vaccinated mice were protected against a lethal challenge of Si/14 virus with no detectable viral lung titers at day 3 post-infection. When challenged with a lethal dose of VN/04 virus, mice vaccinated with IAN-8 rHA had little weight loss and decreased viral lung titers compared to IAN-4, IAN-7, and H-CO2 HA vaccinated mice.
The methodology to generate these next-generation H5 HA vaccines differs from the approach used to generate previous COBRA H5 HA antigens [31] Both traditional and next-generation H5 COBRA HA vaccines induced cross reactive antibodies against multiple H5 viral clades. However, the elicited HAI activity varied between vaccines, as well as the ability to prevent morbidity and mortality in vaccinated mice. The IAN-8 HA vaccine induced antibody titers against 9 out of the 10 H5 viruses derived from different clades. However, antisera collected from gy/WA/14 HA vaccinated had no HAI activity against the VN/04 virus, but~71% of the vaccinated mice survived a lethal VN/04 viral challenge. The immune correlates of protection for H5 have not been as well established as the correlates for seasonal influenza viruses, however, in this study, the antibody titer elicited by the COBRA HA vaccines against a specific strain directly correlated with survival. This inconsistent correlation between low HAI titers and survival appears to be systemic for H5-specific vaccines. Previous studies have also discovered increased survival rates and decreased pathogenicity without detectable serum antibody titers [32,33]. This non-HAI protection has been attributed to stem-based antibodies [34] and/or anti-NA antibodies [35]. However, for this study, only rHA vaccines without NA were included. The role of cellular immunity cannot be ruled out since the use of oil-in-water adjuvants, such as those used in this study, enhances T-cell specific influenza virus vaccine immunity [36,37]. The role of cellular immunity induced by COBRA HA vaccination could be further analyzed.
Previously, mice vaccinated with VLP vaccines expressing the Hu-CO2 HA did not survive challenge and the collected antisera did not have HAI activity against the Si/14 virus. However, neutralizing antibody titers were detectable at higher concentrations [30] and the Hu-CO2 HA vaccinated mice survived a challenge. This may be due to increased antibody titers against HA specific epitopes, since these vaccines lack of NA and Gag p24 core proteins that are included in VLP vaccine formulations. The Hu-CO2 COBRA HA vaccine decreased the pathogenicity induced by the H5N6 influenza virus infection. IAN-8 HA vaccine appears to elicit immune responses against 2.3.2.1 H5Nx influenza viruses and future studies could be performed to demonstrate if IAN-8 HA induced immune responses protect against highly pathogenic variants of H5N6 or H5N8.
A p-epitope analysis of the three-vaccine strains was performed in order to examine the specific epitopes that were essential for HAI titer elicitation (Supplementary Figure S3). P-epitope values were plotted against HAI titers for IAN-4, IAN-7 and IAN-7 HA against the HA in the two challenge VN/04 and Si/14 viruses. The specific H5 HA antigenic sites are not as well defined as the regions on seasonal influenza HA proteins, such as H1N1 and H3N2 subtypes. For this study, we defined the antigenic sites according to the review article by Velkov et al. [38] that described a broad guideline for antigenic sites that are designated as antigenic sites using an overlapping monoclonal antibody approach [38]. The amino acid 282 was also included in the analysis [39,40]. A modification in the methodology was performed in order to calculate the p-epitope value, as described previously [41][42][43][44]. The p-epitope was calculated using only the sites associated with a receptor binding site (RBS). This is an important tool that can be used when designing vaccines against pandemic strains of viruses.
When designing the next-generation COBRA HA vaccines, the goal was to produce unique HA proteins that encompassed not only the 2.3.4.4 clade, but also other clades that are circulating in avian species, specifically viruses in clade 2.3.2.1 that are circulating in Bangladesh, China and India [2]. These results strongly suggest that the IAN-8 rHA vaccine in combination with an oil-in-water adjuvant is a potential candidate for pre-clinical trials against clade 2. Supplementary Materials: The following are available online at https://www.mdpi.com/article/ 10.3390/pathogens10111352/s1, Figure S1: Amino Acid sequences represented from each vaccine. Figure S2: Virus HAI antibody panel from next generation COBRA vaccines., Figure S3: P-epitope analysis of HAI data plotted against amino acid sequence similarity, Table S1: Table of