Patent Application
20220118077
The present disclosure relates to the research, design and production of engineered vaccines, in particular to a broad-spectrum anti-influenza virus vaccine immunogen and the uses thereof, including a novel immunogen, a recombinant vector vaccine and an immunization method thereof.
Influenza is an acute respiratory infectious disease caused by influenza virus infection, which is extremely contagious and fast-spreading. Influenza virus belongs to the Orthomyxoviridae family and is antisense single-stranded RNA virus. Seasonal influenza caused by influenza virus and frequent while unpredictable influenza pandemics have seriously endangered human health and public health. According to the World Health Organization (WHO) report statistics, 3 to 5 million people worldwide are infected with influenza A virus each year, of which there are about 250,000 to 500,000 deaths. Due to the frequent outbreaks of highly pathogenic influenza such as H5N1, H1N1, H3N2, H7N9 in recent years, it is of great significance to develop a universal influenza vaccine that has a cross-protective effect on different subtypes of influenza viruses.
The most effective and economical way to prevent influenza is vaccination. The influenza vaccines currently approved by the World Health Organization are all seasonal influenza vaccines, and most of the international research hotspots in connection with influenza vaccine are focused on inducing antibody responses against influenza virus envelope hemagglutinin protein (HA) to achieve protection. Although the HA head has a substantial immunological advantage in inducing the production of neutralizing antibody, this part is most prone to antigenic drift. Therefore, the neutralizing antibody against the HA head has strong strain specificity, and the virus will mutate selectively towards escaping neutralizing antibody, making it difficult for the antibody to achieve cross-protection. In recent years, studies have found some broad-spectrum neutralizing antibodies that target the HA rod, but they lack cross-protection against different groups of influenza viruses. Due to the subdominance of the immunogenicity of the HA rod in the natural infection state and the weak neutralizing capability against the virus, it is difficult to successfully apply such neutralizing antibodies. Studies have currently confirmed that in H7N9 influenza patients, influenza-specific CD8+ T cells have a broad-spectrum anti-influenza effect and can kill cells infected by different subtypes of influenza. Moreover, after influenza infection, influenza virus antigen-specific CD8+ memory T cells can remain in the respiratory tract for up to one year, and the number of such population of specific CD8+ cells is related to the host's cross-protection capability against influenza infection, offering a theoretical basis for the design of highly efficient and broad-spectrum antiviral influenza vaccines.
The influenza vaccines currently approved by the WHO are all seasonal influenza vaccines, among which the most widely used is the trivalent inactivated vaccine, which contains two influenza A viruses (H1N1 and H3N2) and one influenza B virus. In addition, vaccines administered subcutaneously and live attenuated vaccines administered by nasal spray are also approved for use. However, there is a common challenge for these vaccines, that is, the protective effect of the vaccine depends on the consistency between the prevailing influenza strain in that year and the vaccine strain. Influenza viruses continue to mutate, and WHO's monitoring and forecasting are time-consuming, laborious and inaccurate. In order to ensure the seasonal supply of vaccines, production must be carried out at least seven or eight months in advance, which greatly increases the uncertainty of vaccine prediction. Also, such vaccines are basically ineffective for the pandemic influenza that may occur. The current vaccine production still mainly relies on chicken embryos, with a long production cycle as well as a complicated, time-consuming, laborious and costly process. There are currently a number of strategies available for attempting to construct influenza vaccines, among which the commonly used inactivated vaccines and live attenuated vaccines lack effectiveness, with a complicated production process and a long production time.
DNA vaccines and viral vector vaccines are currently widely used. DNA vaccines have been proven to be the most effective form of primary immunization. The use of DNA vaccine for primary immunization and protein vaccine or viral vector vaccine for boosting is also the hotspot of research on immunization strategies. Currently, the most commonly used adenovirus vaccine vector is human type 5 adenovirus. Although such adenovirus is well capable of expressing foreign genes, it is easily neutralized by the pre-existing adenovirus antibodies in most human bodies due to its human origin, rendering the vaccine ineffective, and thereby limiting the use of such vaccine vector. In recent years, a gorilla-derived type 68 adenovirus vaccine vector has been discovered. There are very few antibodies against this adenovirus in the human body, which overcomes the above problems. Moreover, gorilla type 68 adenovirus can infect dividing and non-dividing cells, but also can transduce lung cells, liver cells, bone cells, blood vessels, muscles, brain, central nervous cells, etc. The type 68 adenovirus is superior in terms of gene stability and expression of foreign genes. It can be produced in large quantities with HEK293 cells and has been widely used in the research of AIDS, Ebola, influenza, malaria, hepatitis C and other vaccines. The Tiantan strain poxvirus vaccine vector has a wide host range, high reproduction titer, and a long-lasting immune response induced. Besides, the capacity for inserting foreign genes into such vector is extremely large, theoretically up to 25-50 kb. The Tiantan strain poxvirus can effectively stimulate the body to produce antibody response and T cell immune response. Due to its proven excellent safety profile, such vaccine vector can also be used by individuals with immunodeficiency.
Therefore, a severe challenge for the current broad-spectrum influenza vaccine is how to design an immunogen against the CD8 T cell epitope(s) within the influenza virus by taking advantage of the internal conserved proteins of influenza virus efficiently, and also to stimulate the immune system more comprehensively, effectively and lastingly through a variety of different vaccine vectors and their combined immunization strategies, leading to a wider range of effective protection.
In one aspect of the present disclosure, there is provided an anti-influenza vaccine immunogen, wherein the immunogen comprises the amino acid sequences shown in SEQ ID No: 1 and SEQ ID No: 2 or an immunogenic fragment thereof, or a combination thereof.
In a specific embodiment of the present disclosure, the immunogen comprises internal conserved proteins of influenza virus, or immunogenic fragments of the conserved proteins.
In another specific embodiment of the present disclosure, the internal conserved proteins of influenza virus include influenza virus matrix protein (M1, M2), nucleoprotein (NP), alkaline polymerase (PB1, PB2) and acid polymerase (PA).
In another specific embodiment of the present disclosure, the immunogen is derived from recombinant proteins of all influenza virus subtypes, or recombinant proteins of shared sequences thereof, or a combination thereof and the influenza virus subtypes include H1, H2, H3, H4, H5, H6, H7, H8, H9, H10, H11, H12, H13, H14, H15, H16, H17, H18 subtypes, and type B influenza virus.
In another aspect of the present disclosure, an anti-influenza vaccine is provided, which is a recombinant vector vaccine expressed and constructed in multiple different vectors by using the above-mentioned anti-influenza vaccine immunogen or an immunogenic fragment thereof.
In a specific embodiment of the present disclosure, the recombinant vector vaccine comprises a recombinant protein vaccine, a recombinant DNA vaccine, a recombinant virus vector vaccine, a recombinant bacterial vector vaccine, a recombinant yeast vector vaccine or a recombinant virus-like particle vaccine, etc.; the virus vector comprises an adenovirus vector, a poxvirus vector, an adeno-associated virus vector, a herpes simplex virus vector, and a cytomegalovirus vector, etc.
In yet another aspect of the present disclosure, an immunization method is provided for constructing a recombinant influenza vaccine for immunization using the above-mentioned anti-influenza vaccine immunogen or an immunogenic fragment thereof, comprising the step of sequential administration with the above-mentioned different recombinant vector vaccines for each immunization, wherein each recombinant vector vaccine is administered at least once, and the vaccination process at least involves one respiratory tract administration and one systemic administration.
In a specific embodiment of the present disclosure, a recombinant vaccine derived from a different vector is used for each shot during the above-mentioned vaccination process.
In a specific embodiment of the present disclosure, the vaccination is performed by means of “primary-boost-re-boost” with each recombinant vaccine administered at least once, and the vaccination process at least involves one respiratory tract administration and one systemic administration.
In a specific embodiment of the present disclosure, during the above-mentioned vaccination process, the mode of systemic administration includes intramuscular injection, subcutaneous administration, and intradermal administration; while the mode of respiratory tract administration includes atomization and nasal drop.
In a specific embodiment of the present disclosure, the above-mentioned vaccination process is as follows: primary vaccination with recombinant DNA vaccine via intramuscular injection, boosting with recombinant adenovirus vector vaccine via the respiratory tract, and reboosting with recombinant poxvirus vaccine via intramuscular injection.
In a specific embodiment of the present disclosure, the recombinant poxvirus vaccine is used as the last shot for the vaccination process.
In a specific embodiment of the present disclosure, the interval between every two shots is at least 1 week, preferably 2 weeks or more.
The vaccine and vaccination technique of the present disclosure can be used to vaccinate poultry to prevent the spread of avian influenza to human; to vaccinate human to reduce the pathogenicity of human infection with avian influenza; to vaccinate human to reduce the pathogenicity of human infection with human influenza; and also to vaccinate human to prevent human-to-human transmission of influenza.
In yet another aspect of the present disclosure, a method for treatment of tumor is provided, comprising intratumoral administration with the above-mentioned anti-influenza vaccine, wherein the tumor comprises lung cancer, liver cancer, kidney cancer, pancreatic cancer, gastric cancer, breast cancer, esophageal cancer, bladder cancer, and osteosarcoma.
In yet another aspect of the present disclosure, an immunization method is provided, wherein the above-mentioned anti-influenza vaccine is used as an adjuvant for other vaccines to enhance the immune response against other immunogens, wherein the other vaccines comprise anti-viral vaccines and anti-tumor vaccines. The other vaccines further comprise anti-ZIKV, anti-hepatitis B, anti-hepatitis C, anti-tuberculosis, anti-HIV, anti-malaria, and anti-dengue fever vaccines, etc. The other vaccines further comprise anti-lung cancer, liver cancer, kidney cancer, pancreatic cancer, gastric cancer, breast cancer, esophageal cancer, bladder cancer, and osteosarcoma vaccines.
In another aspect of the present disclosure, there is provided the use of said anti-influenza vaccine immunogen or an immunogenic fragment thereof or a combination thereof in the preparation of an anti-influenza virus vaccine.
In yet another aspect of the present disclosure, there is provided the use of said anti-influenza vaccine immunogen or an immunogenic fragment or a combination thereof as an adjuvant for other vaccines.
The present disclosure provides a broad-spectrum anti-influenza virus immunogen or an immunogenic fragment thereof or a combination thereof and an immunization method, characterized in that: the immunogen sequence comprises amino acid sequences as shown in SEQ ID No: 1 and SEQ ID No: 2, or an immunogenic fragment thereof, wherein the two sequences can be used separately or concurrently, used as a whole or in the form of a truncated immunogenic fragment, and the immunogenic fragment is equally biologically active as the sequences of the present disclosure. The immunogen sequence of the present disclosure contains influenza virus-specific CD8+ T cell epitopes that bind to human MHC class I molecule with high affinity. Recombinant vaccines have been constructed using the above-mentioned immunogen by means of a variety of different vaccine vectors. Each immunization uses different recombinant vector vaccines for sequential administration. Each recombinant vaccine is administered at least once. The vaccination process at least involves one respiratory tract administration and one systemic administration. The combination of the employed recombinant vector vaccines and administration mode can lead to a high level of T cell immune response in the respiratory tract and whole body system, such that vaccinators can obtain immunity against different subtypes of influenza.
The immunogen of the present disclosure is a recombinant protein comprising the internal conserved matrix protein (M1, M2), nucleoprotein (NP), alkaline polymerase (PB1, PB2) and acid polymerase (PA) of influenza virus, or an immunogenic fragment thereof. The immunogen sequences of the present disclosure are two sequences, named as SEQ ID No: 1 and SEQ ID No: 2 respectively.
The immunogen of the present disclosure can be used to construct recombinant vector vaccines with different vaccine vectors, including but not limited to recombinant protein vaccines, recombinant DNA vaccines, recombinant virus vector vaccines, recombinant bacterial vector vaccines, recombinant yeast vector vaccines or recombinant virus-like particle vaccines, etc.
The immunization method of the multiple recombinant vector vaccines of the present disclosure is implemented by means of “primary-boost-re-boost”, that is, an immunization approach that combines systemic administration and local respiratory tract administration. Each immunization uses different vector vaccines for sequential administration. According to the characteristics of different vector vaccines, the present disclosure preferably uses the following vaccination process: primary vaccination with recombinant DNA vaccine via intramuscular injection to establish systemic immune response, then boosting with recombinant adenovirus type 68 vaccine via the respiratory tract, and finally re-boosting with recombinant poxvirus vaccine via intramuscular injection to establish systemic immune response. The present disclosure preferably uses re-boosting with recombinant poxvirus vector vaccine as the third shot, which can effectively establish a broad-spectrum influenza-specific immune response in the local respiratory tract and the whole body system, and help to enhance the broad-spectrum protection of the vaccine. The interval between every two shots is at least 1 week, and it can be 2 weeks or more.
The mode of systemic administration of the present disclosure includes, but not limited to, intramuscular injection, subcutaneous injection, and intradermal injection, etc.; while the mode of local respiratory tract administration includes, but not limited to, atomization and nasal drop, etc.
The immunogen as described in the present disclosure can be used in the research, design and production of vaccines and drugs for preventing or treating influenza virus infections in birds and mammals. In addition, the immunization method of the present disclosure can induce high-level antigen-specific CD8+ T cell responses in the local respiratory tract; as such, there is a promising prospect for preventing respiratory pathogen infection, reducing the pathogenicity of respiratory pathogens, and preventing and treating respiratory tumors.
The advantages of the present disclosure include the following: the immunogen contains highly conserved influenza CD8 T cell epitopes that bind to human MHC class I molecules with high affinity, and can induce broad-spectrum and high-level influenza-specific T cell immune response; the immunogen can effectively address influenza virus escaping the host's existing immune response due to antigen drift and antigen transformation, and has a cross-protective effect on different subtypes of influenza virus.
The advantages of the present disclosure further include the following: the immunization method adopts a variety of distinct vectors for sequential administration, and utilizes different administration modes to effectively activate the broad-spectrum T cell immune response in the respiratory tract and the whole body system, so as to enhance the vaccine's protective effect on different subtypes of influenza virus.
The advantages of the present disclosure further include the following: the immunogen and immunization method can be used for the vaccination of any respiratory pathogen vaccines; meanwhile, the recombinant vaccine prepared by the immunogen using a viral vector can be employed for the treatment of tumor via intratumor administration, including but not limited to lung cancer, liver cancer, kidney cancer, pancreatic cancer, gastric cancer, breast cancer, esophageal cancer, bladder cancer, osteosarcoma and the like.
The present disclosure will now be specifically described by way of the following examples.
Other aspects of the present disclosure are described in detail below. These and other features and advantages of the present disclosure will become apparent upon reading the detailed description of the embodiments disclosed below and the appended claims.
Unless otherwise defined, all technical and scientific terms used herein have the meanings commonly understood by those skilled in the art to which the present disclosure belongs.
The GenBank database is a gene sequence database established by the National Center for Biotechnology Information (NCBI), through which the gene sequences of about 40,000 strains of influenza virus can be retrieved.
The amino acid sequences of M1, M2, NP, PB1, PB2, and PA proteins interior to the above-mentioned about 40,000 strains of influenza viruses were computationally analyzed, and the amino acid with the highest frequency at each position of the amino acid sequence was regarded as the shared amino acid at that position. The shared amino acids at individual sites constitute the shared amino acid sequence of the protein, thus resulting in the shared amino acid sequences of M1, M2, NP, PB1, PB2, and PA proteins.
The online CD8 T cell epitope prediction software was used to analyze the shared amino acid sequences of PB1, PB2 and PA obtained above. The online software used is derived from http://tools.immuneepitope.org/main/tcell/ and http://www.syfpeithi.de/. The common CD8 T cell epitopes predicted by the two software programs were set aside, and then joined to form the amino acid epitope sequences of PB1, PB2 and PA.
Based on the resulting amino acid sequences above, the vaccine sequence was designed. The PA and PB1 amino acid epitope sequences obtained by epitope joining were combined with shared amino acid sequence of M1 protein to obtain an vaccine amino acid sequence, named SEQ ID No: 1. The PB2 amino acid epitope sequence obtained by epitope joining was combined with shared amino acid sequences of NP and M2 proteins to obtain an another vaccine amino acid sequence, named SEQ ID No: 2.
The above amino acid sequences SEQ ID No: 1 and SEQ ID No: 2 are translated into nucleic acid sequences, and the nucleic acid sequence is optimized for eukaryotic codon via http://www.jcat.de/ online software, resulting in the nucleic acid sequences of SEQ ID No: 1 and SEQ ID No: 2, which were synthesized by Suzhou GENEWIZ Biotechnology Co., Ltd. The synthesized sequences was sequenced by Suzhou GENEWIZ Biotechnology Co., Ltd and verified to be the sequences SEQ ID No: 1 and SEQ ID No: 2 of the present disclosure.
The immunogen of the present disclosure was used to construct a recombinant DNA vector vaccine, a recombinant adenovirus vector vaccine and a recombinant poxvirus vector vaccine.
The immunogen SEQ ID No: 1 or SEQ ID No: 2 of the present disclosure was inserted into the pSV1.0 vector (preserved by Shanghai Public Health Clinical Center) to construct a recombinant DNA vector vaccine, named pSV1.0-SEQ ID No: 1 and pSV1.0-SEQ ID No: 2 respectively.
The immunogen SEQ ID No: 1 or SEQ ID No: 2 was inserted into the AdC68 adenovirus vector (purchased from Institut Pasteur of Shanghai, Chinese Academy of Sciences) and transfected into 293a cells (purchased from the Cell Resource Center of the Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences) to construct a recombinant adenovirus vector vaccine, named AdC68-SEQ ID No: 1 and AdC68-SEQ ID No: 2 respectively.
Immunogens SEQ ID No: 1 and SEQ ID No: 2 were linked using cleavage peptide p2a, inserted into pSC65 vector (preserved by Shanghai Public Health Clinical Center), and transfect into TK143 cells (purchased from the Cell Resource Center of the Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences) to construct a recombinant poxvirus vector vaccine named TTV-SEQ ID No: 1/2.
The expression of anti-influenza vaccine immunogen was detected by Western blotting and the specific steps are as follows:
(1) Preparation of Experimental Samples
PSV1.0-SEQ ID No: 1 or pSV1.0-SEQ ID No: 2 was respectively transfected into 293T cells (purchased from the Cell Resource Center of Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences), and 293T cells were collected 48 hours later. The collected cells were resuspended with 75 microliters of cell lysate followed by addition of 25 microliters of protein loading buffer. Samples were prepared in a water bath at 100° C. for 10 minutes.
AdC68-SEQ ID No: 1 or AdC68-SEQ ID No: 2 was respectively transfected into 293A cells, and 293A cells were collected 24 hours later. The collected cells were resuspended with 75 microliters of cell lysate followed by addition of 25 microliters of protein loading buffer. Samples were prepared in a water bath at 100° C. for 10 minutes.
TTV-SEQ ID No: 1/2 was transfected into TK143 cells, which were collected 48 hours later. The collected cells were resuspended with 75 microliters of cell lysate followed by addition of 25 microliters of protein loading buffer. Samples were prepared in a water bath at 100 degrees Celsius for 10 minutes.
(2) Western blotting: 8% polyacrylamide separation gel was prepared and left at room temperature for 30 minutes. 10% polyacrylamide concentrated gel was added immediately followed by gentle insertion of a comb. The resulting gel was left for 30 minutes until solidified, followed by loading into electrophoresis tank. The electrophoresis buffer was poured into the tank, with slow removal of the comb. The samples prepared as above were loaded sequentially. The electrophoresis was run for half an hour at 70V voltage and then at 90V for an additional 1.5 hours. After activating the polyvinylidene fluoride membrane in methanol for 30 seconds, the sponge, filter paper and polyvinylidene fluoride membrane were soaked with the transfer buffer, and were set up in sequence. The gel and ice bag were placed into the transfer tank which was then filled with the pre-cooled transfer buffer. The transfer was run at a constant current of 200 mA for 2.5 hours. Upon completion, the polyvinylidene fluoride membrane was removed and blocked in 5% skimmed milk powder for 1 hour. The influenza matrix protein 1 antibody (purchased from Abcam (Shanghai) Trading Co., Ltd.) at a dilution of 1:1000 and matrix protein 2 antibody at a dilution of 1:250 (Santa Cruz Biotechnology (Shanghai) Co., Ltd.) were added respectively. After incubating for 2 hours at room temperature on a shaker, the membrane was washed with Tween-20 in phosphate buffer for 3×5 minutes. Then, the horseradish peroxidase-labeled goat anti-mouse IgG antibody at a dilution of 1:5000 was added. After incubating for 1 hour at room temperature on a shaker, the membrane was washed with 5×5 minutes. The developer solution was prepared and then covered onto the polyvinylidene fluoride membrane for luminescence detection.
The immunogen expression results detected by Western blotting were shown in
As described in Example 2, the immunogen of the present disclosure was used to construct DNA vaccines, adenovirus vector vaccines, and poxvirus vector vaccines. The recombinant influenza vaccine was used to immunize mice, and four weeks after completion of the vaccination, the immunogenicity of the recombinant influenza vaccine was evaluated.
The 6-week-old C57BL/6 mice were randomly divided into 3 groups, named control group, adenovirus group and poxvirus group. The specific vaccination procedures are shown in Table 1. The mode of administration was intramuscular injection. The administration dose was 100 micrograms for pSV1.0, 1011 virus particles for AdC68, 50 micrograms for each of pSV1.0-SEQ ID No: 1 and pSV1.0-SEQ ID No: 2, 5×1010 virus particles for each of AdC68-SEQ ID No: 1 and AdC68-SEQ ID No: 2, while 107 plaque forming units for TTV-SEQ ID No: 1/2. The interval between two shots was two weeks.
The immunogenicity of recombinant influenza vaccines was tested in mouse spleen cells using enzyme-linked immunospot assay (ELISpot) and intracellular staining of cytokines (ICS) method.
According to the epitope prediction for SEQ ID No: 1 and SEQ ID No: 2, and the reported common influenza T cell epitopes, 16 epitope monopeptides were selected to stimulate the T cell immune response in mouse, designated as: M1-1, M1-2, M1-3, M2, NP-1, NP-2, NP-3, PB1-1, PB1-2, PB1-3, PB2-1, PB2-2, PB2-3, PA-1, PA-2, and PA-3 respectively.
(1) The Procedures for Enzyme-Linked Immunospot Assay are as Follows:
One day before the experiment, mouse interferon gamma protein was diluted to a final concentration of 5 μg/ml, added 100 μl per well to the assay plate, and coated overnight at 4° C. The next day, the coating solution was discarded. Wells were washed once with 200 microliters of complete medium for each well. Then, 200 microliters of complete medium was added for blocking at room temperature for 2 hours. Upon completion, the concentration of mouse spleen cells was adjusted to 4×106 cells per milliliter. Each well was added 50 microliters of spleen cells, then 50 microliters of 10 μg/ml monopeptide, for incubation in an incubator for about 20 hours. Upon completion, wells were washed twice with 200 microliters of distilled water for each well, and then washed 3 times with 200 microliters of Tween-20 in phosphate buffer. The anti-mouse interferon gamma biotin was diluted to a final concentration of 2 g/ml, added 100 microliters each well for incubation at room temperature for 2 hours. Upon completion, wells were washed 3 times with 200 microliters of Tween-20 in phosphate buffer for each well. The horseradish peroxidase fluorescent substrate was diluted 1:100, added 100 microliters each well for incubation at room temperature for 1 hour. Upon completion, each well was washed 4 times with 200 microliters of Tween-20 in phosphate buffer, and then washed twice with 200 microliters of phosphate buffer. The developer solution was prepared and added 100 microliters each well, allowing to react at room temperature for about 15 minutes in the dark. When clear red spots occurred, the plate was gently rinsed with tap water for 5 minutes to stop the chromogenic reaction. After drying at room temperature, the plate was placed into the enzyme-linked immunospot plate reader for reading and the number of positive spots was counted.
(2) The Procedures for Intracellular Factor Staining are as Follows:
The mouse spleen cells were diluted to 2×107 cells per milliliter. Each well was added 150 microliters of cells and 150 microliters of peptide library, then 1 microliter of CD107a antibody. After incubating for 1 hour, each well was added 0.3 microliters protein transport blocking agent for incubation in an incubator for 6 hours. Upon completion, cells were collected into a flow tube, and then centrifuged at 800 rpm for 3 minutes. The cells were washed with 800 μl staining buffer per tube and centrifuged at 800 rpm for 3 minutes. The supernatant was discarded. CD3, CD8, cell viability/cytotoxicity staining antibody mixture was prepared. Each tube was added 40 microliters of the antibody mixture and stained for 20 minutes at room temperature in the dark. Upon completion, each tube was washed twice with 800 microliters of staining buffer, centrifuged at 800 rpm for 3 minutes. The washing solution was discarded, followed by the addition of 150 microliters of fixative per tube for fixation at room temperature for 20 minutes in the dark. Each tube was washed with 800 microliters of staining buffer, centrifuged at 800 rpm for 3 minutes. The supernatant was discarded. The interferon gamma and tumor necrosis factor alpha staining antibody mixture was prepared. Each tube was added 40 microliters of the antibody mixture and stained for 20 minutes at room temperature in the dark. Each tube was washed with 800 microliters of staining buffer, centrifuged at 1200 rpm for 3 minutes. After the supernatant was discarded, the cells were resuspended in 250 microliters of staining buffer and detected by flow cytometry. Statistical results were analyzed.
The results of the vaccine immunogenicity test are shown in
The results of the enzyme-linked immunospot assay showed that for the control group mice, spot-forming cells were not seen with no influenza-specific T cell immune response; for the adenovirus group mice, more spot-forming cells against the two epitopes of NP-2 and PB2-1 were seen with a higher level T cell immune response; while for the poxvirus group mice, spot-forming cells were seen against NP-2, NP-3, PB1-1, PB1-3, PA-3 and other epitopes with a higher T cell immune response.
Intracellular factors interferon gamma, tumor necrosis factor alpha, and CD107a staining were used to detect influenza-specific immune response level in mouse spleen cells. The results showed that there were no T cells expressing interferon gamma, tumor necrosis factor alpha, and CD107a in the control group; while T cells expressing interferon gamma, tumor necrosis factor alpha, and CD107a were found in both the adenovirus group and the poxvirus group, thus demonstrating influenza-specific T cell immune response.
This Example confirmed that the expression of anti-influenza vaccine immunogens SEQ ID No: 1 and SEQ ID No: 2 through different vaccine vectors can induce significant T cell immune responses.
As described in Example 2, the immunogen of the present disclosure was used to construct DNA vaccines, adenovirus vector vaccines, and poxvirus vector vaccines. As described in Example 3, the recombinant influenza vaccine was used to immunize mice, and four weeks after completion of the vaccination, the protective effect of the recombinant influenza vaccine upon challenge was evaluated.
The H1N1 and H7N9 influenza challenge models were used to evaluate the protective effect of the immunogen. The H1N1 influenza challenge experiment was carried out in the biosafety level-2 laboratory, and the H7N9 influenza challenge experiment was carried out in the biosafety level-3 laboratory.
Each mouse was anesthetized by intraperitoneal injection of 50 microliters of 10% chloral hydrate, and each mouse was challenged with 50 microliters nasal drops of influenza virus. The challenge dose for H1N1 influenza virus was 500 TCID50 (median tissue culture infective dose) per mouse. The challenge dose for H7N9 influenza virus was 100 TCID50 per mouse. On the 5th day after the challenge, 5 mice in each group were sacrificed, and the lungs were taken for virus load determination.
The results of the challenge-protection results are shown in
After a lethal dose challenge of H1N1 influenza virus, mice in the control group continued to lose weight and all reported death on the 12th day. The mice in the adenovirus group began to recover on the 9th day and all survived to 14 days. For the poxvirus group, the weight loss of the mice significantly slowed down; the body weight began to rise on the 9th day; and all mice survived to 14 days.
After a non-lethal dose challenge of H7N9 influenza virus, mice in the control group lost nearly 20% of their body weight and recovered on the 9th day. Mice in the adenovirus group and poxvirus group lost less than 10% of their body weight, and their body weight recovered rapidly on the 7th day.
This Example confirmed that the expression of anti-influenza vaccine immunogens SEQ ID No: 1 and SEQ ID No: 2 through different vaccine vectors can produce cross-protective effects against H1N1 and H7N9 influenza viruses, that is, the immunogen of the present disclosure has a broad-spectrum protective effect against different subtypes of influenza virus.
As described in Example 2, the immunogen of the present disclosure was used to construct DNA vaccines, adenovirus vector vaccines, and poxvirus vector vaccines. The immunization method of the present disclosure is used to immunize mice. Four weeks after completion of the vaccination, the immunogenicity test was performed according to the method described in Example 3.
The 6-week-old C57BL/6 mice were randomly divided into 5 groups, designated as control group 1, control group 2, control group 3, experimental group 1, and experimental group 2 respectively, in which experimental group 1 and experimental group 2 adopted the immunization method of the present disclosure. The specific vaccination procedures are shown in Table 2. The administration dose was 100 micrograms for pSV1.0, 1011 virus particles for AdC68, 50 micrograms for each of pSV1.0-SEQ ID No: 1 and pSV1.0-SEQ ID No: 2, 5×1010 virus particles for each of AdC68-SEQ ID No: 1 and AdC68-SEQ ID No: 2, while 107 plaque forming units for TTV and TTV-SEQ ID No: 1/2. The interval between two shots was two weeks.
The results of the vaccine immunogenicity test are shown in
The results of the enzyme-linked immunospot assay showed that in the spleen cells of mice, for the control group mice, spot-forming cells were not seen with no influenza-specific T cell immune response; for each single peptide in the control group 2, 3 and experimental group 1 and 2, spot-forming cells were seen with a high level of T cell immune response. In mouse lung lavage fluid, no spot-forming cells were seen in the control group 1, 2 and 3, and influenza-specific immune response could not be established in the lung; more spot-forming cells were seen in the experimental group 1 and 2, demonstrating that experimental group 1 and experimental group 2 using the vaccination method of the present disclosure showed a very high level of influenza-specific T cell immune response.
Intracellular factors interferon gamma, tumor necrosis factor alpha, and CD107a staining were used to detect influenza-specific immune response level in mouse spleen cells. The results showed that there were no T cells expressing interferon gamma and tumor necrosis factor alpha in control group 1, while T cells expressing interferon gamma and tumor necrosis factor alpha were found in control group 2, 3 and experimental group 1 and 2, thus exhibiting influenza-specific T cell immune response.
This Example confirmed that through the sequential administration of different recombinant vector vaccines, and the combination of the respiratory tract and systemic immunization, the experimental group 1 and the experimental group 2 using the vaccination method of the present disclosure can effectively establish a high level of influenza-specific immune response in both the whole body system and the local lung, which is superior to that of the control group.
According to the method described in Example 5, the immunization method of the present disclosure was used to immunize mice, and four weeks after the last shot for the mouse, H1N1 and H7N9 influenza challenge models were used to evaluate the protective effect of the immunogen. The H1N1 influenza challenge experiment was carried out in the biosafety level-2 laboratory, and the H7N9 influenza challenge experiment was carried out in the biosafety level-3 laboratory.
Each mouse was anesthetized by intraperitoneal injection of 50 microliters of 10% chloral hydrate, and each mouse was challenged with 50 microliters nasal drops of influenza virus. The challenge dose for H1N1 influenza virus was 500 TCID50 (median tissue culture infective dose) per mouse. The challenge dose for H7N9 influenza virus was 500 TCID50 per mouse. On the 5th day after the challenge, 5 mice in each group were sacrificed, and the lungs were taken for virus load determination.
The results of the challenge-protection results are shown in
After the H1N1 influenza virus challenge, all mice in the control group 1 died on the 13th day, while the control groups 2 and 3 showed partial protective effects, in which 80% and 60% of the mice survived to the 14th day, respectively. The weight of mice in experimental group 1 and experimental group 2 using the vaccination method of the present disclosure recovered on the 10th day, and all survived to the 14th day, in which the viral load of the experimental group 2 was significantly reduced, showing an excellent protective effect.
After the H7N9 influenza virus challenge, the weight of mice in experimental group 1 and experimental group 2 using the vaccination method of the present disclosure quickly recovered on the 10th day, and all the mice survived to the 14th day, showing an excellent protective effect. No apparent protective effect was seen in other groups of mice.
This Example confirmed that through the sequential administration of different recombinant vector vaccines, and the combination of the respiratory tract and systemic immunization, experimental group 1 and experimental group 2 using the vaccine immunization method of the present disclosure showed excellent cross-protective effects against H1N1 and H7N9 influenza viruses; and its protective effect is superior to that of control group 2 and control group 3 which merely use one route of intramuscular injection. Moreover, when the recombinant poxvirus vector vaccine was used as the last shot of vaccine, the protective effect of the vaccine is optimal.
According to the method described in Example 5, the immunization method of the present disclosure was used to immunize mice. Four weeks after the last shot for the mouse, the H1N1 and H7N9 influenza challenge models were used to evaluate the protective effect of the immunogen. The specific procedures for influenza virus attack are described in Example 6. Throughout the challenge process, the mice were continuously offered with drinking water containing 2 μg/ml FTY720. FTY720 is an immunosuppressant that can effectively reduce the number of peripheral circulating lymphocytes and retain the lung colonization of tissue in situ memory T cells established by nasal inoculation. FTY720 was continuously used during the challenge with a lethal dose of H1N1 and H7N9 influenza viruses in order to evaluate whether the nasal inoculation showed a strengthening effect.
The experimental results are shown in
Upon H1N1 and H7N9 influenza virus challenge, the experimental group 1+FTY720 and the experimental group 2+FTY720 both showed partial protection. The weight of the mice began to rise on the 11th day and survived to the 14th day with a reduction in viral load. The protective effect in the experiment groups is superior to that of the control group 1+FTY720.
This Example confirmed that the administration mode via respiratory tract can effectively enhance the protective effect of the vaccine against H1N1 and H7N9 influenza.
The present disclosure is not limited to the above-mentioned embodiments, and those skilled in the art will understand that various modifications, additions, and substitutions can be made without departing from the scope and spirit of the present invention disclosed in the appended claims.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2018/105020 | 9/11/2018 | WO | 00 |
