Patent Application
20130022637
The present invention provides a novel transfer vector, a recombinant baculovirus obtained by homologous recombination of the transfer vector and a baculovirus DNA and methods for production thereof.
The present invention also relates to pharmaceuticals (e.g., vaccines, preventive or therapeutic drugs for infectious diseases such as malaria and influenza) comprising the recombinant baculovirus as an active ingredient.
Baculovirus has been used as a vector in methods of industrially producing a desired protein using insect cells. In recent years, it has been found that baculovirus can introduce a foreign gene not only into insect cells but also into mammalian cells, and the possibility of their use as a vector for introducing a therapeutic gene has been found. In Patent document 1, a recombinant baculovirus expression vector having multiple independent promoters composed of a DNA region comprising a gene encoding a viral non-structural protein in the promoter derived from an early gene from the baculovirus and a DNA region comprising a gene encoding a viral structural protein in the promoter derived from a late gene has been disclosed.
In Patent document 2, the method in which a non-mammalian DNA virus comprising a promoter controlled so that an exogenous gene is expressed from a vector in which the desired exogenous genes have been linked to the multiple independent promoters is introduced into a cell and the exogenous gene is expressed in the mammalian cell has been disclosed.
Furthermore, in Patent document 3, the method of producing the protein by gene recombination technology using the baculovirus has been disclosed, and the method of producing the protein by expressing a fusion gene obtained by linking a gp64 gene of the baculovirus to a gene encoding the desired protein, producing the desired protein in a form in which the desired protein has been fused to viral particles, collecting the viral particles fused with the desired protein, and cleaving the desired protein from the viral particles to collect the desired protein has been disclosed.
In Patent document 4, for a baculovirus expression system, a recombinant baculovirus expression vector having multiple independent promoters comprising a first nucleic acid sequence encoding a detection marker linked in the form capable of functioning to a first promoter which is active in a host cell and is inactive in a non-acceptable cell, and a second nucleic acid sequence comprising a foreign nucleic acid sequence linked in the form capable of functioning to a second promoter which is active in the non-acceptable cell has been disclosed.
In patent document 5, it has been disclosed that an influenza virus hemagglutinin (HA) antigen-expressing recombinant baculovirus vector linked to a CAG promoter derived from chicken β actin is useful as a vaccine formulation because the vector has a preventive effect on infection with influenza virus.
In Patent document 6, the method of producing a baculovirus vector comprising a co-transfection step in which a plasmid in which genes encoding proteins expressible on the cell surface have been linked to the baculovirus promoter and the promoter derived from the mammalian cell, respectively, and a plasmid in which genes encoding proteins expressible on the cell surface have been linked to two baculovirus promoters, respectively are co-transfected in the insect cell has been disclosed.
And in patent document 7, a study on an anti-influenza virus activity on the infection with influenza virus using the recombinant baculovirus in which cDNA from influenza virus HA has been incorporated in the CAG promoter has been disclosed, and it has been disclosed that not only the recombinant baculovirus but also a wild type baculovirus has the activity.
This way, in recent years, various recombinant baculoviruses have been developed, and pharmaceutical development for mammals using them has been studied utilizing the recombinant baculovirus as the active ingredient.
In the related art, a recombinant baculovirus vector having a novel structure, and the development of a pharmaceutical formulation, particularly a vaccine formulation using the recombinant baculovirus as the active ingredient, which is effective for infectious diseases such as malaria and influenza, or diseases such as cancer have been desired.
An object of the present invention is to provide a novel recombinant transfer vector, a recombinant baculovirus obtained by homologous recombination of the recombinant transfer vector and a baculovirus DNA, and methods for production thereof. Another object of the present invention is to provide a pharmaceutical preparation, particularly a vaccine formulation containing the recombinant baculovirus as an active ingredient
The present inventors have found a transfer vector having a novel structure capable of expressing a protein having a desired immunogenicity, or a fusion protein of a partial protein or the protein having the immunogenicity with cytokine in insect cells and vertebrate (particularly mammal, bird and fish) cells other than insect cells, and a recombinant baculovirus obtained by homologous recombination of the transfer vector and a baculovirus DNA. By providing the recombinant baculovirus, the pharmaceutical having the recombinant baculovirus as the active ingredient having effective preventive and/or therapeutic effects on infectious diseases was extensively studied. As a result, the present inventors have newly found that the recombinant baculovirus has the effect as the desired pharmaceutical.
And, according to the present invention, the recombinant transfer vector having the novel structure, the recombinant baculovirus obtained by homologous recombination of the transfer vector and the baculovirus DNA and the methods for production thereof were confirmed, and it was confirmed that the recombinant baculovirus itself was useful as the pharmaceutical capable of expressing the protein having the desired immunogenicity in the target cells and was useful as the preventive pharmaceutical for the infectious diseases such as malaria and influenza, and here the present invention was completed.
The present invention provides the invention shown in the following [1] to [51]
[1] A method of producing a transfer vector comprising a structure in which a dual promoter and a fusion gene are incorporated, characterized in that the fusion gene comprising at least one gene encoding a protein capable of being a component of a viral particle and at least one immunogenic foreign gene are linked downstream of the dual promoter linking one vertebrate promoter and another baculovirus promoter.
[2] The method according to [1], wherein the vertebrate promoter is a mammalian promoter.
[3] The method according to [1], characterized in that the gene encoding at least one protein capable of being the component of the viral particle is any of a baculovirus gp64 gene, a Vesicular stomatitis virus glycoprotein gene, a type I human immunodeficiency virus glycoprotein gene, a human respiratory syncytial virus membrane glycoprotein gene, a type A influenza virus hemagglutinin protein gene, a type B influenza virus hemagglutinin protein gene, a herpes simplex virus glycoprotein gene and a murine hepatitis virus S protein gene.
[4] The method according to [1], wherein the vertebrate promoter is selected from any of a cytomegalovirus promoter, an SV40 promoter, a retrovirus promoter, a metallothionein promoter, a heat shock protein promoter, a CAG promoter, an elongation factor 1α promoter, an actin promoter, a ubiquitin promoter, an albumin promoter and an MHC class II promoter.
[5] The method according to [1], wherein the baculovirus promoter is selected from a polyhedrin promoter, a p10 promoter, an IE1 promoter, an IE2 promoter, a p35 promoter, a p39 promoter, and a gp64 promoter.
[6] The method according to [1], wherein the immunogenic foreign gene is selected from any of a malaria antigen, an influenza antigen, an M. tuberculosis antigen, a SARS virus antigen, a West Nile fever virus antigen, a dengue fever virus antigen, an HIV antigen, an HCV antigen, a leishmania antigen, a trypanosoma antigen, a leucocytozoon antigen alone, or a fusion antigen of at least one selected from these antigen gene group with a cytokine.
[7] The method according to [1], wherein the transfer vector is any of pDual-Hsp65-gp64, pDual-PbCSP-gp64, pDual-H1N1/HA1-64, pDual-PbTRAMP-gp64, pDual-PbAMA1D123-gp64, pDual-PbMSP129-64, pDual-PfCSP-64, pDual-PfAMA1-gp64, pDual-Pfs25-gp64, pDual-H5N1/HA1-gp64, pDual-SARS/S-gp64, pCP-H1N1/HA1-gp64, pCAP-H1N1/HA1-gp64, pCU-H1N1/HA1-gp64, pDual-H1N1/NP-gp64, pDual-H1N1/M2-gp64, pDual-H1N1/NAe-gp64, pDual-M2e-gp64, pCP-HA1/NC99-gp64, pCP-H1N1/HA0-gp64, pCP-H1N1/HA2-gp64, pCP-H1N1/HA1-vp39 and pCP-H1N1/NP-vp39, pCAP-PfCSP, pCAP-PfCSP/272, pCAP-PfCSP/467, pCAP-PfCSP(A361E), pCAP-PfCSP(A361E)/272, pCAP-PfCSP(A361E)/467, pCAP-PfCSP-76, pCAP-PfCSP-76/467, pCAP-PfCSP+209, pCAP-PfCSP+209/467, pCAP-PfCSP+76/209, pCAP-PfCSP+76/209/467, pCAP-HA1/Anhui, pCAP-HA1/Anhui/272, pCAP-HA1/Anhui/467, pCAP-HA1/Vietnam, pCAP-HA1/Vietnam/51, pCAP-HA1/Vietnam/101, pCAP-HA1/Vietnam/154, pCAP-HA1/Vietnam/201, pCAP-HA1/Vietnam/272, pCAP-HA1/Vietnam/467, pCAP-AH/345, pCAP-AH/345/467, pCAP-AH/410, pCAP-AH/410/467, pCAP-AH/473, pCAP-AH/473/467, pCAP-AH/520, pCAP-AH/520/467, pCAP-VN/346, pCAP-VN/346/467, pCAP-VN/410, pCAP-VN/410/467, pCAP-VN/473, pCAP-VN/473/467, pCAP-VN/520, pCAP-VN/520/467, pCAP-CO/full, pCAP-CO/full/467, pCAP-CO/19, pCAP-CO/19/467, pCAP-CO/76, pCAP-CO/76/467, pCAP-CO/205, pCAP-CO/205/467, pCA39-HA1/Anhui, pCA64-HA1/Anhui, pCA39-PfCSP(A361E), pCA64-PfCSP(A361E), pCAP-CO/full/VSV, pCAP-CO/19/VSV, pCAP-CO/76/VSV, pCAP-CO/205/VSV, pDual-Pfs25-PfCSP-gp64, and pDual-PfMSP1-PfCSP-gp64.
[8] A method of producing a recombinant baculovirus comprising the steps of producing a transfer vector comprising a structure in which a dual promoter and a fusion gene are incorporated, characterized in that the fusion gene comprising at least one gene encoding a protein capable of being a component of a viral particle and at least one immunogenic foreign gene are linked downstream of the dual promoter linking one vertebrate promoter and another baculovirus promoter; co-transfecting the transfer vector and a baculovirus DNA into a host cell of an insect; and separating the recombinant baculovirus.
[9] The method according to [8], characterized in that the gene encoding at least one protein capable of being the component of the viral particle is any of a baculovirus gp64 gene, a Vesicular stomatitis virus glycoprotein gene, a type I human immunodeficiency virus glycoprotein gene, a human respiratory syncytial virus membrane glycoprotein gene, a type A influenza virus hemagglutinin protein gene, a type B influenza virus hemagglutinin protein gene, a herpes simplex virus glycoprotein gene and a murine hepatitis virus S protein gene.
[10] The method according to [9], wherein the vertebrate promoter is selected from any of a cytomegalovirus promoter, an SV40 promoter, a retrovirus promoter, a metallothionein promoter, a heat shock protein promoter, a CAG promoter, an elongation factor 1α promoter, an actin promoter, a ubiquitin promoter, an albumin promoter and an MHC class II promoter.
[11] The method according to [8], wherein the baculovirus promoter is selected from a polyhedrin promoter, a p10 promoter, an IE1 promoter, a p35 promoter, a p39 promoter, and a gp64 promoter.
[12] The method according to [8], wherein the immunogenic foreign gene is selected from any of a malaria antigen, an influenza antigen, an M. tuberculosis antigen, a SARS virus antigen, a West Nile fever virus antigen, a dengue fever virus antigen, an HIV antigen, an HCV antigen, a leishmania antigen, trypanosoma antigen, a leucocytozoon antigen alone, or a fusion antigen of one selected from these antigen gene group with a cytokine.
[13] The method according to [8], wherein the recombinant baculovirus is any of AcNPV-Dual-Hsp65, AcNPV-Dual-PbCSP, AcNPV-Dual-H1N1/HA1, AcNPV-Dual-PbTRAMP, AcNPV-Dual-PbAMA1D123, AcNPV-Dual-PbMSP129, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39 and AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-gp64, and AcNPV-Dual-PfMSP1-PfCSP-gp64.
[14] A transfer vector comprising a structure in which a fusion gene comprising at least one gene encoding a protein capable of being a component of a viral particle and at least one immunogenic foreign gene were linked downstream of the dual promoter linking one vertebrate promoter and another baculovirus promoter is incorporated.
[15] The transfer vector according to [14], characterized in that the gene encoding at least one protein capable of being the component of the viral particle is any of a baculovirus gp64 gene, a Vesicular stomatitis virus glycoprotein gene, a type I human immunodeficiency virus glycoprotein gene, a human respiratory syncytial virus membrane glycoprotein gene, a type A influenza virus hemagglutinin protein gene, a type B influenza virus hemagglutinin protein gene, a herpes simplex virus glycoprotein gene and a murine hepatitis virus S protein gene.
[16] The transfer vector according to [14], wherein the vertebrate promoter is selected from any of a cytomegalovirus promoter, an SV40 promoter, a retrovirus promoter, a metallothionein promoter, a heat shock protein promoter, a CAG promoter, an elongation factor 1α promoter, an actin promoter, a ubiquitin promoter, an albumin promoter and an MHC class II promoter.
[17] The transfer vector according to [14], wherein the baculovirus promoter is selected from a polyhedrin promoter, a p10 promoter, an IE1 promoter, an IE2 promoter, a p35 promoter, a p39 promoter, and a gp64 promoter.
[18] The transfer vector according to [14], wherein the immunogenic foreign gene is selected from any of a malaria antigen, an influenza antigen, an M. tuberculosis antigen, a SARS virus antigen, a West Nile fever virus antigen, a dengue fever virus antigen, an HIV antigen, an HCV antigen, a leishmania antigen, a trypanosoma antigen, a leucocytozoon antigen alone, or a fusion antigen of one selected from these antigen gene group with a cytokine.
[19] The transfer vector according to [14], which is any of pDual-Hsp65-gp64, pDual-PbCSP-gp64, pDual-H1N1/HA1-gp64, pDual-PbTRAMP-gp64, pDual-PbAMA1D123-gp64, pDual-PbMSP129, pDual-PfCSP-gp64, pDual-PfAMA1-gp64, pDual-Pfs25-gp64, pDual-H5N1/HA1-gp64, pDual-SARS/S-gp64, pCP-H1N1/HA1-gp64, pCAP-H1N1/HA1-gp64, pCU-H1N1/HA1-gp64, pDual-H1N1/NP-gp64, pDual-H1N1/M2-gp64, pDual-H1N1/NAe-gp64, pDual-M2e-gp64, pCP-HA1/NC99-gp64, pCP-H1N1/HA0-gp64, pCP-H1N1/HA2-gp64, pCP-H1N1/HA1-vp39 and pCP-H1N1/NP-vp39, pCAP-PfCSP, pCAP-PfCSP/272, pCAP-PfCSP/467, pCAP-PfCSP(A361E), pCAP-PfCSP(A361E)/272, pCAP-PfCSP(A361E)/467, pCAP-PfCSP-76, pCAP-PfCSP-76/467, pCAP-PfCSP+209, pCAP-PfCSP+209/467, pCAP-PfCSP+76/209, pCAP-PfCSP+76/209/467, pCAP-HA1/Anhui, pCAP-HA1/Anhui/272, pCAP-HA1/Anhui/467, pCAP-HA1/Vietnam, pCAP-HA1/Vietnam/51, pCAP-HA1/Vietnam/101, pCAP-HA1/Vietnam/154, pCAP-HA1/Vietnam/201, pCAP-HA1/Vietnam/272, pCAP-HA1/Vietnam/467, pCAP-AH/345, pCAP-AH/345/467, pCAP-AH/410, pCAP-AH/410/467, pCAP-AH/473, pCAP-AH/473/467, pCAP-AH/520, pCAP-AH/520/467, pCAP-VN/346, pCAP-VN/346/467, pCAP-VN/410, pCAP-VN/410/467, pCAP-VN/473, pCAP-VN/473/467, pCAP-VN/520, pCAP-VN/520/467, pCAP-CO/full, pCAP-CO/full/467, pCAP-CO/19, pCAP-CO/19/467, pCAP-CO/76, pCAP-CO/76/467, pCAP-CO/205, pCAP-CO/205/467, pCA39-HA1/Anhui, pCA64-HA1/Anhui, pCA39-PfCSP(A361E), pCA64-PfCSP(A361E), pCAP-CO/full/VSV, pCAP-CO/19/VSV, pCAP-CO/76/VSV, pCAP-CO/205/VSV, pDual-Pfs25-PfCSP-gp64, and pDual-PfMSP1-PfCSP-gp64.
[20] A recombinant baculovirus produced by the method of producing the recombinant baculovirus according to any of [8] to [13].
[21] The recombinant baculovirus according to [20] which is any of AcNPV-Dual-Hsp65, AcNPV-Dual-PbCSP, AcNPV-Dual-H1N1/HA1, AcNPV-Dual-PbTRAMP, AcNPV-Dual-PbAMA1D123, AcNPV-Dual-PbMSP129, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39 and AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-gp64, and AcNPV-Dual-PfMSP1-PfCSP-gp64.
[22] A pharmaceutical composition comprising the recombinant baculovirus according to [20] or [21].
[23] The pharmaceutical composition according to [22], comprising any of AcNPV-Dual-H1N1/HA1, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39 and AcNPV-CP-H1N1/NP-vp39.
[24] A pharmaceutical composition comprising the recombinant baculovirus according to claim [20] or [21], wherein the composition is administered intramuscularly, intranasally or by inhalation.
[25] A vaccine comprising any of AcNPV-Dual-H1N1/HA1, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39 and AcNPV-CP-H1N1/NP-vp39 as an active ingredient.
[26] A vaccine comprising any one of AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64.
[27] The vaccine according to [25] or [26], wherein the vaccine is administered intramuscularly, intranasally or by inhalation.
[28] A therapeutic or preventive agent for influenza virus infection, comprising AcNPV-Dual-H1N1/HA1, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39 as an active ingredient.
[29] A therapeutic or preventive agent for influenza virus infection, comprising as an active ingredient any one of AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CA39-HA1/Anhui, and AcNPV-CA64-HA1/Anhui.
[30] The therapeutic or preventive agent for influenza virus infection according to [28] or [29], wherein the agent is administered intramuscularly, intranasally or by inhalation.
[31] A vaccine for influenza virus infection, comprising any of AcNPV-Dual-H1N1/HA1, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39 and AcNPV-CP-H1N1/NP-vp39 as an active ingredient.
[32] A vaccine against influenza virus infection, comprising as an active ingredient any one of AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CA39-HA1/Anhui, and AcNPV-CA64-HA1/Anhui.
[33] The vaccine for influenza virus infection according to [31] or [32], wherein the agent is administered intramuscularly, intranasally or by inhalation.
[34] A therapeutic or preventive agent for human malaria infection, comprising as an active ingredient any one of AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64.
[35] A therapeutic or preventive agent for human malaria infection according to [34], which is administered by the intramuscular, respiratory, or nasal route.
[36] A therapeutic or preventive agent for human malaria infection, comprising as an active ingredient any one of AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64.
[37] A therapeutic or preventive agent for human malaria infection according to [36], which is administered by the intramuscular, respiratory, or nasal route.
[38] A method for producing an immunopotential action in a mammal, comprising administrating a recombinant baculovirus produced by the method according to any of [8] to [13] as an active ingredient to the mammal.
[39] The method according to [38], wherein the recombinant baculovirus is any of AcNPV-Dual-Hsp65, AcNPV-Dual-PbCSP, AcNPV-Dual-H1N1/HA1, AcNPV-Dual-PbTRAMP, AcNPV-Dual-PbAMA1D123, AcNPV-Dual-PbMSP129, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39 and AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64.
[40] The method according to [38] or [39], wherein the composition is administered intramuscularly, intranasally or by inhalation.
[41] A method for preventing or treating a virus infection in mammals, comprising administrating a recombinant baculovirus produced by the method according to any of [8] to [13] as an active ingredient to the mammal.
[42] The method according to [41], wherein the recombinant baculovirus is any of AcNPV-Dual-Hsp65, AcNPV-Dual-PbCSP, AcNPV-Dual-H1N1/HA1, AcNPV-Dual-PbTRAMP, AcNPV-Dual-PbAMA1D123, AcNPV-Dual-PbMSP129, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39 and AcNPV-CP-H1N1/NP-vp39.
[43] The method according to [41] or [42], wherein the composition is administered intramuscularly, intranasally or by inhalation.
[44] A method of preventing malaria or influenza infection or of treating malaria or influenza, comprising administering to a subject an effective amount of the recombinant baculovirus of [21], the composition for infectious diseases of claim [22] or [23], or the vaccine of [25], [26], [27], [31], [32] or [33].
[45] A method according to [44], wherein the recombinant baculovirus, composition, or vaccine is administered to the subject as a liposomal formulation.
[46] A method according to [44], wherein the recombinant baculovirus, composition, or vaccine is administered to the subject by the intramuscular, respiratory, or nasal route.
[47] A method according to [45], wherein the recombinant baculovirus, composition, or vaccine is administered to the subject by the intramuscular, respiratory, or nasal route.
[48] A method of immunostimulation comprising administering to a subject an effective amount of the recombinant baculovirus of [21], the composition for infectious diseases of claim [22] or [23], or the vaccine of [25], [26], [27], [31], [32] or [33].
[49] A method according to [48], wherein the recombinant baculovirus, composition, or vaccine is administered to the subject as a liposomal formulation.
[50] A method according to [48], wherein the recombinant baculovirus, composition, or vaccine is administered to the subject by the intramuscular, respiratory, or nasal route.
[51] A method according to [49], wherein the recombinant baculovirus, composition, or vaccine is administered to the subject by the intramuscular, respiratory, or nasal route.
According to the present invention, a novel recombinant transfer vector, a recombinant baculovirus obtained by homologous recombination of the recombinant transfer vector and a baculovirus DNA, and methods for production thereof are provided. Pharmaceuticals comprising the recombinant baculovirus of the present invention as an active ingredient are useful as the therapeutic or preventive drugs for the infectious diseases such as malaria, influenza, tuberculosis and hepatitis, cancers and autoimmune diseases, or as cellular medicine and vaccine formulations.
Lane 1: AcNPV-WT
Lane 2: AcNPV-Dual-H1N1/HA1
Lane 3: AcNPV-WT
Lane 4: AcNPV-Dual-Hsp65
Lane 5: AcNPV-WT
Lane 6: AcNPV-Dual-PbCSP;
(A): HepG2 cells transduced with AcNPV-Dual-Hsp65;
(B): HepG2 cells transduced with AcNPV-WT.
Lane 1: AcNPV-WT
Lane 2: AcNPV-CMV-PbCSP
Lane 3: AcNPV-PbCSPsurf
Lane 4: AcNPV-Dual-PbCSP.
The abbreviations used for the amino acids, peptides, base sequences, and nucleic acids in the present specification are based on the abbreviations specified in the IUPAC-IUB Communication on Biochemical Nomenclature, Eur. J. Biochem., 138: (1984) and “Guideline for Preparing Specifications Including Base Sequences and Amino Acid Sequences” (Patent Office), and those commonly used in this technical field.
A DNA molecule herein encompasses not only double strand DNA but also single strand DNA including sense chains and antisense chains which compose them. The length of DNA is not limited to a length thereof. Therefore, the polynucleotide (DNA molecule) encoding the immunogenic foreign gene of the present invention includes the double strand DNA including genomic DNA and the single strand DNA (sense chain) including cDNA and the single strand DNA (antisense chain) having the sequence complementary to the sense chain and synthetic DNA fragments thereof unless otherwise mentioned.
The polynucleotide or the DNA molecule herein is not limited in the functional region, and can include at least one of an expression suppression region, a coding region, a leader sequence, an exon and an intron.
Further, examples of the polynucleotide include RNA and DNA. The polypeptide containing a specific amino acid sequence and the polynucleotide containing a specific DNA sequence include fragments, homologs, derivatives, and mutants of the polynucleotide.
The mutants of the polynucleotide, e.g., mutant DNA include naturally occurring allelic mutants, not naturally occurring mutants and mutants having deletion, substitution, addition and insertion. But, these mutants encode the polypeptide having substantially the same function as the function of the polypeptide encoded by the polynucleotide before the mutation.
In the present invention, the transfer vector refers to a plasmid for producing the recombinant baculovirus, comprising the structure in which a fusion gene linking at least one gene encoding a protein capable of being a component of a viral particle and at least one immunogenic foreign gene are incorporated as a fusion gene downstream of a dual promoter comprising a vertebrate promoter (mammalian promoter, bird promoter, fish promoter) and a baculovirus promoter which are connected.
In one of the preferable embodiment of the invention, it is preferable that the immunogenic foreign gene is located downstream of the dual promoter and upstream of the gene encoding the protein capable of being the component of the viral particle.
The recombinant baculovirus of the present invention is used as the active ingredient of the pharmaceuticals or vaccines for vertebrates. As the vertebrates, mammals including human beings, e.g., horses, swines, sheeps, goats, monkeys, mice, dogs and cats, birds such as chickens, quails, gooses, dabblers, pigeons, turkeys, pintados and parrots, and fishes such as yellow tails, adult yellowtails, sea breams, amberjacks, scads, striped jacks, striped pigfish, salmons, blueback salmons, carps, crucian carps, rainbow trouts, brook trouts and amago trouts can be exemplified.
In one embodiment, the present invention provides the transfer vector comprising the novel structure in which the fusion gene comprising the gene encoding a viral membrane protein that can be expressed in an insect cell and one immunogenic foreign gene are incorporated as a fusion gene under the control of the dual promoter comprising a vertebrate promoter and a baculovirus promoter which are connected. By co-transfecting this transfer vector together with a baculovirus DNA into an insect cell to induce a homologous recombination, it is possible to obtain the recombinant baculovirus comprising the fusion gene incorporated under the control of the baculovirus promoter, which can express in an insect cell and can produce a fusion protein capable of being the component of the budded viral particle.
In the present invention, when the recombinant baculovirus is administered to a vertebrate, the fusion protein of the protein capable of being the component of the budded viral particle and the immunogenic protein probably functions as a component vaccine. When the recombinant baculovirus administered to a vertebrate invades a vertebrate cell, a fusion antigen with the target immunogenic foreign antigen encoded by the viral genome is produced in the viral genome, and functions as a DNA vaccine.
Therefore, in the case of the mammal, by administering the recombinant baculovirus of the present invention to the mammal, the fusion protein of the protein capable of being the component of the viral particle and the immunogenic protein is presented as antigen and is produced in the cell of the mammal. The fusion protein is thought to function as the preventive or therapeutic agent for infections with virus, protozoa and bacteria due to its immunopotential or immunostimulation action.
The baculovirus DNA to be co-transfected with the transfer vector may be any of a wild type, a mutant and a recombinant baculovirus DNA. Host cells to be co-transfected include, for example, cells from the insect such as Spodoptera frugiperda.
In the present invention, a immunogenic foreign gene is a gene encoding an amino acid sequence of an antigenic protein which can be used as an immunogen of immunotherapy including vaccine therapy for prevention and treatment of infectious diseases, such as malaria, influenza and tuberculosis, autoimmune disease and cancers. Examples of the antigen protein include malaria antigen, influenza virus antigen and M. tuberculosis antigen is referred to as the immunogenic foreign gene.
Here, the “foreign” gene means a gene introduced from outside, including a gene that is originally present in the cell when introduced from outside.
In the present invention, the gene encoding the amino acid sequence of the protein which is the above immunogen is not particularly limited as the gene encoding the amino acid sequence of the antigenic protein as long as the gene is the gene encoding the amino acid sequence of the antigenic protein having the immunogenicity against a substance which causes the diseases such as infectious diseases, cancers and autoimmune diseases. Examples of these genes encoding the amino acid sequence of the antigenic protein having the immunogenicity include the followings.
As the gene encoding the amino acid sequence of the malaria antigen, for example, the genes encoding the amino acid sequences of the proteins such as a surface antigen CSP (Circumsporozoite Protein) of sporozoite surface of malaria parasite, MSP1 (merozoite surface protein 1) of a membrane protein of metrozoite surface, a malaria S antigen secreted from erythrocytes infected with malaria, PfEMP1 protein present in knob of the erythrocytes infected with malaria, SERA protein, TRAMP protein and AMA1 protein are exemplified.
As the gene encoding the amino acid sequence of the influenza virus antigen, the genes encoding the amino acid sequences of the proteins such as HA antigen (hemagglutinin antigen), NA antigen (neuraminidase antigen), M2 antigen (matrix protein antigen) and NP antigen (nucleoprotein antigen) can be exemplified.
As the gene encoding the amino acid sequence of the antigenic protein for tuberculosis, the genes encoding the amino acid sequences of the proteins such as HSP65 (65-kDa heat shock protein), α-antigen (Antigen85A, Antigen85B, Antigen85C), Mtb72f, MDP-1, ESAT-6, MPB51m, Mtb8.8, Mtb9.9, Mtb32, Mtb39 and Mtb11.
With respect to vertebrate genes, as the mammalian genes, the genes encoding the amino acid sequences of the antigenic proteins of the infectious diseases in human beings, cattle, horses, swines, sheeps, monkeys, mice, dogs and cats can be exemplified. As the bird genes, the antigen genes (e.g., bird influenza S antigen) of the infectious diseases in chickens, dabblers, pigeons, turkeys, pintados and parrots can be exemplified. As the fish genes, the antigen genes of the infectious diseases in yellow tails, adult yellowtails, sea breams, amberjacks, scads, striped jacks, striped pigfish, salmons, blueback salmons, carps, crucian carps, rainbow trouts, brook trouts and amago trouts are included.
Pathogen genes whose association with the infectious diseases in the above mammals, birds and fishes has been reported are easily available from the institutions where public data such as GenBank registering the pathogen genes have been stored.
In the present invention, for the immunogenic foreign genes, in addition to the above immune antigens present outside the human body, for example, cytokine genes present inside the human body, e.g., an IL-12 gene, an IL-6 gene, an IL-6 receptor gene, an IL-2 gene, an IL-18 gene, an IFN-γ gene and an M-CSF gene, or fusion genes obtained by fusing a given antigen having the immunogenicity with the above antigenic protein using gene recombination technology are also addressed as the immunogenic foreign genes in the present invention as long as they are introduced from the outside.
In the present invention, it is possible to provide the transfer vector having these immunogenic foreign genes and the recombinant baculovirus obtained by homologous recombination thereof, as well as provide a pharmaceutical composition comprising the recombinant baculovirus having the immunogenic foreign gene as the active ingredient and the vaccine formulation composed of the pharmaceutical composition.
The baculovirus used for the present invention is an insect pathogen virus is in a group of DNA viruses (Baculoviridae) having a cyclic double strand DNA as a gene which causes infection in an insect and is one group (Baculoviridae) of DNA viruses having a cyclic double strand DNA as the gene. Among them, one group of the viruses referred to as a nuclear polyhedrosis virus (NPV) makes an inclusion body referred to as a polyhedron in a nucleus in an infected cell in the late phase of the infection. Even if the foreign gene to be expressed is inserted in place of a polyhedron gene, the virus infects, grows and produces the desired foreign gene product in a large amount with no problem. Thus, this has been practically applied to the production of the desired protein in recent years.
As the baculovirus used for the present invention, Autographa Californica Nuclear Polyhedorosis Virus: AcNPV, Bombyx mori Nuclear Polyhedorosis Virus: BmNPV, Orgyia pseudotsugata Nuclear Polyhedorosis Virus: OpNPV and Lymantria disper Nuclear Polyhedorosis Virus LdNPV can be exemplified.
The baculovirus DNA may be any DNA which can perform the homologous recombination with the transfer vector of the present invention. Specifically, the viral gene of the baculovirus DNA which can perform the homologous recombination with the transfer vector of the present invention is 130 kbp which is huge, and the immunogenic foreign gene of 15 kbp or more can be inserted. The baculovirus gene itself is scarcely expressed in the vertebrate cells. Thus, there is almost no need to consider its cytotoxicity, and thus, it is thought that no harmful immune response is induced.
The immunogenic foreign gene DNA capable of being fused to the viral gene, which is one of the components of the baculovirus transfer vector can be easily produced and acquired by synthesizing based on nucleic acid sequence information of the polynucleotide encoding the amino acid sequence of the antigenic protein having the objective immunogenicity disclosed herein, or directly synthesizing (chemical DNA synthesis method) the DNA corresponding to the nucleic acid sequence of a coding region of the immunogenic foreign gene based on the nucleic acid sequence information of the immunogenic foreign gene. General gene engineering techniques can be applied to this production (e.g., see Molecular Cloning 2d Ed, Cold Spring Harbor Lab. Press(1989); Zoku Seikagaku Jikken Kouza, “Idenshi Kenkyuho I, II, III” edited by the Japanese Biochemistry Society, 1986).
As the synthesis methods of the DNA, chemical synthesis means such as phosphate triester method and phosphate amidite method (J. Am. Chem. Soc., 89, 4801 (1967); ibid., 91, 3350 (1969); Science, 150, 178 (1968); Tetrahedron Lett., 22, 1859 (1981); ibid., 24, 245 (1983)) and combination methods thereof can be exemplified. More specifically, the DNA can also be chemically synthesized by a phosphoramidite method or the triester method, and can be synthesized using a commercially available automatic oligonucleotide synthesizer. A double strand fragment can be obtained by synthesizing a complementary chain and annealing the complementary chain with a chemically synthesized single strand under an appropriate condition or adding the complementary chain with appropriate primer sequences to the chemically synthesized single strand using a DNA polymerase.
As specific one aspect of the immunogenic foreign gene DNA produced in the present invention, DNA composed of the DNA sequence encoding the amino acid sequence of the M. tuberculosis antigen protein, the DNA sequence encoding the amino acid sequence of the malaria antigen protein or the DNA sequence encoding the amino acid sequence of the influenza virus antigen protein can be exemplified.
The DNA utilized in the present invention is not limited to a full length DNA sequence of a DNA sequence encoding the amino acid sequence of a polypeptide of antigenic protein having immunogenicity, and may be a DNA sequence encoding a partial sequence as long as the protein of the amino acid sequence encoded by the DNA sequence has immunogenicity.
The DNA utilized in the present invention may be a DNA sequence obtained by fusing a DNA sequence encoding the amino acid sequence of an antigenic protein having antigenicity to a cytokine gene present inside of human body, e.g., IL-12 gene, IL-1 gene, IL-6 gene, IL-6 receptor gene, IL-2 gene, IL-18 gene, IFN-α gene, IFN-β gene, IFN-γ gene, TNF gene, TGF-β gene, GM-CSF gene and M-CSF gene.
The fused DNA sequence is not limited to a full length of the coding region of a DNA sequence encoding an amino acid sequence of the polypeptide of an antigenic protein having antigenicity and a DNA sequence of a cytokine gene, and may be a partial DNA sequence.
The DNA of the immunogenic foreign gene used for the present invention is not limited to a DNA molecule having such a particular DNA sequence, and can also have a DNA sequence obtained by combining and selecting an optional codon for each amino acid residue. The choice of a codon can be performed in accordance with standard methods. At that time, for example, it is possible to consider a usage frequency of a codon in the host utilized. (Nucleic Acids Res., 9, 43 (1981)).
The method of producing the DNA of immunogenic foreign gene used for the present invention by gene engineering techniques can be more specifically performed by preparing cDNA library from an appropriate origin which expresses the DNA of the immunogenic foreign gene in accordance with standard methods and selecting a desired clone from the library using an appropriate probe or an antibody against an expressed product which is inherent for the immunogenic foreign gene (see Proc. Natl. Acad. Sci., USA., 78, 6613 (1981); Science, 222, 778 (1983)).
In the above, as the origin of the genomic DNA, various cells, tissues and cultured cells derived therefrom which express the DNA of the immunogenic foreign gene can be exemplified. In particular, it is preferable to use an extract of an erythrocytes infected with malaria parasites, an extract of a cells infected with influenza virus or an extract of M. tuberculosis as origin. The extraction and separation of total DNA and RNA from the origin, the separation and purification of mRNA and the acquisition and cloning of cDNA can be performed in accordance with standard methods.
The production of the DNA of the immunogenic foreign gene can also be performed by extracting mRNA of each immunogen, then adding poly A to RNA, collecting the poly A-added RNA, producing cDNA using a reverse transcriptase, adding restriction enzyme sites to both ends of the cDNA and using a phage library prepared by incorporating the cDNA into a phage, in addition to obtaining using cDNA library of each immunogen obtained by the extraction, separation and purification of mRNA from immunogenic tissue or cell using the extract as origin.
The method of screening the DNA of the immunogenic foreign gene from the cDNA library is not particularly limited, and can be performed in accordance with ordinary methods. As a specific method, for example, a method of selecting a corresponding cDNA clone by immunological screening using a specific antibody (e.g., anti-malaria antibody, anti-influenza virus antibody, anti-M. tuberculosis antibody) against the protein produced by the cDNA; a plaque hybridization method using a probe selectively binding to the objective DNA sequence; a colony hybridization method; and the combinations thereof can be exemplified.
As a probe used in hybridization methods, DNA fragments chemically synthesized based on the information for the DNA sequence of the immunogenic foreign gene are common. The immunogenic foreign gene already acquired and the DNA sequences of fragments thereof can be advantageously utilized as the above probe. Furthermore, a sense primer and an antisense primer designed based on the DNA sequence information of the immunogenic foreign gene can also be used as the probe for the above screening.
The DNA (nucleotides) used as the probe is the partial DNA (nucleotides) corresponding to the DNA sequence of the immunogenic foreign gene, and has at least 15 consecutive DNA, preferably at least 20 consecutive DNA and more preferably at least 30 consecutive DNA. A positive clone itself for producing the above DNA can also be used as the probe.
When the DNA of the immunogenic foreign gene is acquired, a DNA/RNA amplification method by PCR (Science, 230, 1350 (1985)) can be utilized suitably. In particular, when a full length cDNA is hardly obtained from the library, RACE method [Rapid amplification of cDNA ends; Jikken Igaku 12(6), 35 (1994)], in particular, 5′-RACE method [M. A. Frohman, et al., Proc. Natl. Acad. Sci., USA., 8, 8998 (1988)] is suitably employed.
A primer used for PCR can be designed based on the DNA sequence information of the immunogenic foreign gene, and synthesized in accordance with standard methods. As this primer, as shown in Examples described later, DNA portions (SP6 promoter primer and T7 terminator primer) added to both ends of the vector plasmid in which the DNA of the immunogenic foreign gene is incorporated in can also be used.
The isolation/purification of the DNA/RNA fragment amplified by PCR can be performed in accordance with standard methods, e.g., gel electrophoresis.
For the DNA of the immunogenic foreign gene obtained as the above or various DNA fragments, their DNA sequences can be determined in accordance with standard methods, e.g., dideoxy method (Proc. Natl. Acad. Sci., USA., 74, 5463 (1977)) or Maxam-Gilbert method (Methods in Enzymology, 65, 499 (1980)), or simply using a commercially available sequencing kit.
Any gene can be used as a gene encoding an amino acids of a protein capable of being the component of a viral particle, as long as it is the gene encoding a protein that can be expressed as the protein capable of being the component of the viral particle in an insect cell and as a fusion protein by fusing the immunogenic foreign gene in the objective cell.
As the gene encoding the amino acids of the protein capable of being the component of the viral particle, for example, the genes of a gp64 protein (GenBank Accession No. L22858), a Vesicular stomatitis virus glycoprotein (GenBank Accession No. M21416), a herpes simplex virus glycoprotein (KOS; GenBank Accession No. K01760), a type I human immunodeficiency virus gp120 (GenBank Accession No. U47783), a human respiratory syncytial virus membrane glycoprotein (GenBank Accession No. M86651), a type A influenza virus hemagglutinin protein (GenBank Accession No. U38242), or the gene of envelop proteins of viruses closely related to the baculovirus can be exemplified. In the present invention, the gp64 gene shown in Examples described later can be preferably exemplified.
The DNA of the gene encoding the amino acids of the protein capable of being the component of the viral particle can be easily produced and acquired by synthesizing based on the nucleic acid sequence information of the polynucleotide encoding the amino acid sequence of the polypeptide of the gene encoding the amino acids of the objective protein capable of being the component of the viral particle, or by directly synthesizing the DNA corresponding to the nucleotide sequence encoding the amino acid sequence based on the amino acid sequence information of the gene encoding the amino acids of the protein capable of being the component of the viral particle (chemical DNA synthesis) as is the case with the production of the DNA of the immunogenic foreign gene.
A DNA sequence corresponding to a nucleic acid sequence encoding amino acids of a protein capable of being a component of a viral particle is not limited to a full length of a coding region, and may be a DNA composed of a partial DNA sequence.
As is the case with the production of the DNA molecule of the immunogenic foreign gene, the DNA of the gene encoding the amino acids of the protein capable of being the component of the viral particle can be produced by general gene engineering techniques (e.g., see Molecular Cloning 2d Ed, Cold Spring Harbor Lab. Press(1989); Zoku Seikagaku Jikken Kouza, “Idenshi Kenkyuho I, II, III” edited by the Japanese Biochemistry Society, 1986).
In the present invention, a commercially available vector plasmid in which a part of the promoter which controls the expression of the immunogenic foreign gene described later is previously incorporated and the gene (portion) encoding the amino acids of the protein capable of being the component of the viral particle is previously introduced can also be used.
As the vertebrate promoter (capable of functioning in vertebrates) which is one of the components of the transfer vector used for the present invention, the promoters such as mammalian promoters, bird promoters and fish promoters can be exemplified.
As a mammalian promoter (capable of functioning in mammals) which is one of the components of the transfer vector used for the present invention, a cytomegalovirus promoter, an SV40 promoter, a retrovirus promoter, a metallothionein promoter, a heat shock protein promoter, a CAG promoter, an elongation factor la promoter, an actin promoter, a ubiquitin promoter, an albumin promoter and an MHC class II promoter can be exemplified.
As bird promoters, a β actin promoter, a heat shock protein promoter, an elongation factor promoter, a ubiquitin promoter and an albumin promoter can be exemplified.
As fish promoters, an actin promoter, a heat shock protein promoter and an elongation factor promoter can be exemplified.
As a baculovirus promoter which is one of the components of the baculovirus transfer vector used for the present invention, a polyhedrin promoter, a p10 promoter, an IE1 promoter, a p35 promoter, a p39 promoter, and a gp64 promoter can be exemplified.
The present invention relates to a novel transfer vector having a structure that can express the desired immunogenic foreign gene as antigenic protein in both an insect cell and a vertebrate cell, particularly a mammalian cell. In the present invention, the structure of the novel transfer vector is characterized in that the DNA sequence encoding the amino acid sequence of the desired immunogenic protein and the DNA sequence encoding the amino acid sequence of the protein capable of being the component of the viral particle are incorporated downstream of the dual promoter comprising a vertebrate promoter, particularly a mammalian promoter, and a baculovirus promoter, which are connected. DNA regions comprising the DNA sequences of two promoters; one is a vertebrate promoter, particularly a mammalian promoter and another is a baculovirus promoter. These two promoters may be directly linked, or an intervening DNA sequence may be present between the DNA sequences of the two promoters. However, in the latter case, each promoter needs to have activities in an insect cell and a vertebrate cell, particularly in a mammalian cell. In the promoter region, either the vertebrate promoter, particularly the mammalian promoter or the baculovirus promoter can be placed in the closer region to the gene to be expressed. In Examples described later, the baculovirus is placed in closer region to the gene to be expressed than the mammalian promoter.
In the said structure, the DNA sequence of the fusion gene of a gene encoding a protein capable of being a component of viral particles and a desired immunogenic foreign gene may be such that these two genes are directly linked to each other, or an intervening DNA sequence is present between the genes. In the latter case, however, it is necessary not to cause a frameshift of the downstream gene and the upstream gene. Preferably, the antigen-presenting domain of the protein of a foreign gene having the desired immunogenicity is fused to a protein capable of being a component of viral particles. Therefore, the protein of a foreign gene having the desired immunogenicity should not be cut off from the protein capable of being a component of viral particles, but should be used in a fused form.
A fusion gene comprising these two genes may be formed in advance and this may be incorporated in the vector. Alternatively, one gene may be incorporated in the vector in advance, and subsequently the other gene may be incorporated in the vector to form the fusion gene in the vector.
To produce such a transfer vector, commercially available expression vectors having essential components of the transfer vector of the present invention, i.e., a promoter region containing a vertebrate promoter, particularly a mammalian promoter, and a baculovirus promoter, and a gene region encoding the amino acid sequence of a protein capable of being a component of viral particles, may be used. The required components can be inserted by cleaving such a commercially available expression vector arbitrarily with restriction enzymes and incorporating other promoter to insert a fused DNA sequence of a foreign gene having the desired immunogenicity and a gene encoding the amino acid sequence of a protein capable of being a component of viral particles into the cloning region of the vector, or by inserting a foreign gene having the desired immunogenicity into the N terminus side of the DNA region of a gene encoding the amino acid sequence of a protein capable of being a component of viral particles, which is previously incorporated in a plasmid.
For the detection of the protein, a His-tag or an HVS-tag may be added upstream of a poly A tail at a C terminus side of the DNA sequence fusing the desired immunogenic foreign gene to the gene encoding the amino acid sequence of the protein capable of being the component of the viral particle. Alternatively, for the expression, the purification or the detection of the recombinant fusion protein, the DNA sequence encoding a FLAG sequence composed of 8 amino acids may be inserted as a peptide tag between the promoter region and the region in which the desired immunogenic foreign gene is fused to the gene encoding the amino acid sequence of the protein capable of being the component of the viral particle. In the present invention, the plasmid vector having the structure that can express the desired immunogenic foreign protein as antigenic protein in both an insect cell and a vertebrate cell, particularly a mammalian cell, may be produced by using a commercially available plasmid that has a part of the structure. The amino acid sequence of the peptide may intervene for cleaving the fusion protein with the enzyme in a vertebrate cell. In the transfer vector of the present invention, an enhancer for increasing a transcription activity in a vertebrate cell, particularly the mammalian cell, may be placed upstream of the two promoters, or the DNA sequence encoding the amino acid sequence of a signal peptide for facilitating extracellular secretion of the expressed protein in hosts may be bound to the gene to be fused and expressed. A vertebrate terminator region, e.g., a rabbit β globulin terminator which is effective in the vertebrate cell may be placed for terminating the transcription downstream the gene to be fused and expressed.
As the above, the transfer vector capable of expressing the fusion gene of the immunogenic foreign gene capable of expressing the desired immunogenicity in the baculovirus particle and the gene encoding the amino acid sequence of the protein capable of being the component of the viral particle can be produced.
Specific examples of the transfer vector and the method for production thereof according to the present invention are as shown in the Examples described later. More specifically, as transfer vectors having a structure; in which a vertebrate promoter (particularly as a mammalian promoter) such as a cytomegalovirus (CMV) promoter, a CAG promoter modified from CMV promoter and a ubiquitin (UBB) promoter fused CMV enhancer, and a baculovirus promoter such as a polyhedrin (polh) promoter, vp39 promoter and gp64 promoter are linked, and the DNA sequence, in which foreign genes such as influenza virus antigen gene, malaria antigen gene and M. tuberculosis antigen gene and a gene encoding the amino acid sequence of the protein capable of the component of the viral particle such as gp64 antigen gene are fused, is inserted: pDual-Hsp65-gp64, pDual-PbCSP-gp64, pDual-H1N1/HA1-gp64, pDual-PbTRAMP-gp64, pDual-PbAMA1D123-gp64, pDual-PbMSP129-gp64, pDual-PfCSP-gp64, pDual-PfAMA1-gp64, pDual-Pfs25-gp64, pDual-H5N1/HA1-gp64 and pDual-SARS/S-gp64, pCP-H1N1/HA1-gp64, pCAP-H1N1/HA1-gp64, pCU-H1N1/HA1-gp64, pDual-H1N1/NP-gp64, pDual-H1N1/M2-gp64, pDual-H1N1/NAe-gp64, pDual-M2e-gp64, pCP-HA1/NC99-gp64, pCP-H1N1/HA0-gp64, pCP-H1N1/HA2-gp64, pCP-H1N1/HA1-vp39, pCP-H1N1/NP-vp39, pCAP-PfCSP, pCAP-PfCSP/272, pCAP-PfCSP/467, pCAP-PfCSP(A361E), pCAP-PfCSP(A361E)/272, pCAP-PfCSP(A361E)/467, pCAP-PfCSP-76, pCAP-PfCSP-76/467, pCAP-PfCSP+209, pCAP-PfCSP+209/467, pCAP-PfCSP+76/209, pCAP-PfCSP+76/209/467, pCAP-HA1/Anhui, pCAP-HA1/Anhui/272, pCAP-HA1/Anhui/467, pCAP-HA1/Vietnam, pCAP-HA1/Vietnam/51, pCAP-HA1/Vietnam/101, pCAP-HA1/Vietnam/154, pCAP-HA1/Vietnam/201, pCAP-HA1/Vietnam/272, pCAP-HA1/Vietnam/467, pCAP-AH/345, pCAP-AH/345/467, pCAP-AH/410, pCAP-AH/410/467, pCAP-AH/473, pCAP-AH/473/467, pCAP-AH/520, pCAP-AH/520/467, pCAP-VN/346, pCAP-VN/346/467, pCAP-VN/410, pCAP-VN/410/467, pCAP-VN/473, pCAP-VN/473/467, pCAP-VN/520, pCAP-VN/520/467, pCAP-CO/full, pCAP-CO/full/467, pCAP-CO/19, pCAP-CO/19/467, pCAP-CO/76, pCAP-CO/76/467, pCAP-CO/205, pCAP-CO/205/467, pCA39-HA1/Anhui, pCA64-HA1/Anhui, pCA39-PfCSP(A361E), pCA64-PfCSP(A361E), pCAP-CO/full/VSV, pCAP-CO/19/VSV, pCAP-CO/76/VSV, pCAP-CO/205/VSV, pDual-Pfs25-PfCSP-gp64, and pDual-PfMSP1-PfCSP-gp64 can be exemplified.
The present invention provides a method of producing a recombinant baculovirus comprising a step of producing a transfer vector having a structure in which a fusion gene containing at least one gene encoding a protein capable of being a component of the viral particle and at least one immunogenic foreign gene is incorporated downstream of a dual promoter comprising two linked promoters, i.e., a vertebrate promoter and a baculovirus promoter; and a step of co-transfecting the transfer vector and a baculovirus DNA into a host cell and isolating the recombinant baculovirus.
In the above method of producing the recombinant baculovirus, methods of introducing the desired recombinant DNA (transfer vector) into the host and methods of transforming therewith are not particularly limited, and various methods which are well known and commonly used can be employed. Such methods can be performed in accordance with the ordinary gene recombination technology (e.g., Science, 224, 1431 (1984); Biochem. Biophys. Res. Comm., 130, 692 (1985); Proc. Natl. Acad. Sci. USA, 80, 5990 (1983). The recombinant DNA (transfer vector) can be expressed and produced with reference to Ohno et al., “Tanpaku Jikken Protocol 1 Functional analysis, Saibo Kogaku Bessatu Jikken Protocol Series, 1997, Shujunsha”. For general techniques of handling of the insect cells, gene recombination and co-transfection, the same techniques as in the well-known methods of making recombinant virus in insect cells can be used (Zenji Matsuura, Proteins, Nucleic acids and Enzymes, 37:211-222, 1992; Zenji Matsuura, Saibo 33(2):30-34, 2001).
The resulting recombinant baculovirus can be cultured in accordance with the standard methods. By culturing, a fusion product (expressed product) in which the DNA of the immunogenic foreign gene and the DNA encoding the amino acid sequence of the protein capable of being the component of the viral particle of the present invention are fused designed as desired is expressed, produced (accumulated) or secreted inside, outside the cells or on the cell membrane.
As a medium used for the culture, various media commonly used can be appropriately selected and used depending on the host cells employed, and the culture can be performed under the condition suitable for growth of the host cells.
More specifically, the method of producing the recombinant baculovirus comprises the step of preparing the baculovirus DNA for performing the homologous recombination with the transfer vector produced above and the step of co-transfecting the transfer vector and the baculovirus DNA in the insect cells such as Sf-9 cells, Sf-21 cells derived from Spodoptera frugiperda, Tn5 cells (High Five cells supplied from Invitrogen) derived from Trichoplusia ni as the host cells.
The baculovirus DNA produced above for performing the homologous recombination with the transfer vector may be any of the wild type, the mutant or the recombinant baculovirus DNA.
A baculovirus DNA can enhance a probability of homologous recombination as long as it has the DNA structure homologous to the DNA derived from the baculovirus DNA located upstream of the dual promoters used for the transfer vector so as to produce the homologous recombination with the transfer vector of the present invention, except for the DNA derived from a baculovirus which sandwiches a fusion gene in which DNA in the dual promoter region, the immunogenic foreign gene and the gene encoding the protein capable of being the component of the viral particle are fused.
To induce the homologous recombination, it is better that the transfer vector and the baculovirus DNA is mixed at a weight ratio of about 1:1 to 10:1.
After introducing into the insect cell simultaneously by the step of co-transfection and culturing the cell, plaques of the virus are made from the culture supernatant, then suspended in the medium, subsequently the virus is eluted from the agar by vortex to yield a solution comprising the recombinant virus.
In the above, the commercially available baculovirus DNA may be used, and for example, it is possible to use BacVector-1000 DNA and BacVector-2000 DNA (supplied from Novagen) in which the polyhedrin gene is removed from AcNPV.
The co-transfection of the transfer vector and the baculovirus DNA obtained above in the insect cell for the homologous recombination can be performed using the commercially available vector transfection kit described above (BacVector Transfection Kits supplied from Novagen) in accordance with instructions attached to the vector transfection kit. As the above, the transfer vector produced above can be co-transfected together with the baculovirus DNA in the insect cell such as Sf-9 cell to yield the recombinant baculovirus.
In the present invention, in accordance with the above method of producing the recombinant baculovirus, the transfer vectors such as pDual-Hsp65-gp64, pDual-PbCSP-gp64, pDual-H1N1/HA1-gp64, pDual-PbTRAMP-gp64, pDual-PbAMA1D123-gp64, pDual-PbMSP129-gp64, pDual-PfCSP-gp64, pDual-PfAMA1-gp64, pDual-Pfs25-gp64, pDual-H5N1/HA1-gp64, pDual-SARS/S-gp64, pCP-H1N1/HA1-gp64, pCAP-H1N1/HA1-gp64, pCU-H1N1/HA1-gp64, pDual-H1N1/NP-64, pDual-H1N1/M2-gp64, pDual-H1N1/NAe-gp64, pDual-M2e-gp64, pCP-HA1/NC99-gp64, pCP-H1N1/HA0-gp64, pCP-H1N1/HA2-gp64, pCP-H1N1/HA1-vp39, pCP-H1N1/NP-vp39, pCAP-PfCSP, pCAP-PfCSP/272, pCAP-PfCSP/467, pCAP-PfCSP(A361E), pCAP-PfCSP(A361E)/272, pCAP-PfCSP(A361E)/467, pCAP-PfCSP-76, pCAP-PfCSP-76/467, pCAP-PfCSP+209, pCAP-PfCSP+209/467, pCAP-PfCSP+76/209, pCAP-PfCSP+76/209/467, pCAP-HA1/Anhui, pCAP-HA1/Anhui/272, pCAP-HA1/Anhui/467, pCAP-HA1/Vietnam, pCAP-HA1/Vietnam/51, pCAP-HA1/Vietnam/101, pCAP-HA1/Vietnam/154, pCAP-HA1/Vietnam/201, pCAP-HA1/Vietnam/272, pCAP-HA1/Vietnam/467, pCAP-AH/345, pCAP-AH/345/467, pCAP-AH/410, pCAP-AH/410/467, pCAP-AH/473, pCAP-AH/473/467, pCAP-AH/520, pCAP-AH/520/467, pCAP-VN/346, pCAP-VN/346/467, pCAP-VN/410, pCAP-VN/410/467, pCAP-VN/473, pCAP-VN/473/467, pCAP-VN/520, pCAP-VN/520/467, pCAP-CO/full, pCAP-CO/full/467, pCAP-CO/19, pCAP-CO/19/467, pCAP-CO/76, pCAP-CO/76/467, pCAP-CO/205, pCAP-CO/205/467, pCA39-HA1/Anhui, pCA64-HA1/Anhui, pCA39-PfCSP(A361E), pCA64-PfCSP(A361E), pCAP-CO/full/VSV, pCAP-CO/19/VSV, pCAP-CO/76/VSV, pCAP-CO/205/VSV, pDual-Pfs25-PfCSP-gp64, and pDual-PfMSP1-PfCSP-gp64, and the baculovirus DNA were used and co-transfected in the Sf-9 insect cell to yield the recombinant baculoviruses such as AcNPV-Dual-Hsp65, AcNPV-Dual-PbCSP, AcNPV-Dual-H1N1/HA1, AcNPV-Dual-PbTRAMP, AcNPV-Dual-PbAMA1D123, AcNPV-Dual-PbMSP129, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-00/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64.
Also, the recombinant baculoviruses such as AcNPV-Dual-H5N1/HA1 and AcNPV-Dual-SARS/S can be obtained.
In addition to the above method of producing the recombinant baculovirus, as the other method of producing the recombinant baculovirus, it is possible to use the method of inserting the foreign gene efficiently in Escherichia coli by utilizing a transposon for a phagemid (bacmid) in which the entire baculovirus genome is incorporated. According to the method, the recombinant baculovirus can be easily produced and collected by only extracting the bacmid bearing the viral gene from microbial cells and transfecting it in the insect cell.
The purification of the recombinant baculovirus of the present invention obtained by the above method of producing the recombinant baculovirus can be performed using the virus purification method known publicly.
For the purification of the recombinant baculovirus, for example, 0.5 to 1.0 mL of a stock virus (usually 1×107-8 pfu/mL) obtained by the above method of producing the recombinant baculovirus is inoculated to the insect cells (1×107 cells/10 cm dish) such as Sf-9 cells, the culture supernatant is collected several days (4 days) after the infection, and a virus pellet obtained by centrifugation is suspended in buffer such as PBS. The resulting suspension is applied on sucrose gradient of 10 to 60%, which is then centrifuged (25,000 rpm, 60 minutes, 4° C.) to collect a virus band. The collected virus is further suspended in PBS, subsequently centrifuged (same condition as the above), and the resulting purified recombinant virus pellet is stored in the buffer such as PBS at 4° C.
An infectivity titer of the above resulting purified recombinant virus can be measured by plaque assay (Fields VIROLOGY 4th Edition p29-32 2001; BACULOVIRUS EXPRESSION VECTORS: A LABORATORY MANUAL, Oxford University Press, 1994) using the insect cells such as Sf-9 cells.
In the recombinant virus exemplified in the present invention, the N terminus of the baculovirus protein gp64 is exposed outside the particle and its C terminus is exposed inside the particle. Thus, if the protein encoded by the desired immunogenic foreign gene is fused to the N terminus of gp64, its entirety is exposed outside the viral protein particle as the component of the viral particle in an insect cell, and thus the antigen is more easily presented, which is suitable for the object of the vaccine formulation of the present invention.
The recombinant baculovirus of the present invention which is the active ingredient in the pharmaceutical composition of the present invention can be obtained by the gene engineering techniques shown in the above (2).
It is important that the pharmaceutical composition of the present invention contain as the active ingredient the recombinant baculovirus obtained by homologous recombination of the baculovirus DNA and the transfer vector constructed, and that the transfer vector is constructed so that the fusion gene of the immunogenic foreign gene and the gene encoding the amino acid sequence of the protein capable of being the component of the viral particle can be expressed in the insect cells and the vertebrate cells, particularly cells from mammals including human being.
In particular, the present invention provides the pharmaceutical composition comprising any of the particular recombinant baculovirus, such as AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-gp64, or AcNPV-Dual-PfMSP1-PfCSP-gp64 as active ingredient.
The recombinant baculovirus of the present invention, such as AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64 which is the active ingredient in the pharmaceutical composition of the present invention has the actions which enhances an infection-preventing effect on the infectious antigen and reduces the infectivity titer, and this action or activity can be utilized to treat diseases associated with the infection of target cells or tissues. Such target cells affected by the infection include, for example blood cells, and other target cells include hepatic cells, renal cells, brain cells, lung cells, epithelial cells and muscular cells. The tissues comprising these cells include lung, liver, kidney, arterial and venous veins, stomach, intestine, urethra, skin and muscle.
The pharmaceutical composition enhances infection-preventing effects against infectious antigens, for example, malaria antigens such as sporozoite surface antigens (CSP and TRAP) of malaria parasites, merozoite surface membrane protein MSP1, malaria S antigen secreted from erythrocytes infected with malaria, PfEMP1 protein present in the knobs of erythrocytes infected with malaria, SERA protein, TRAMP protein, AMA1 protein, and Pfs25 known as a transmission-blocking antigen; and influenza antigens such as HA antigen, NA antigen, M2 antigen, and NP antigen, and reduces the infectivity titer (e.g., viral infectivity titer), thereby increasing the survival period and survival rate of mammals including humans, compared to the group not administered the pharmaceutical composition of the present invention. Therefore, the pharmaceutical composition is particularly useful as a preventive or therapeutic agent for malaria and influenza virus infections.
The pharmaceutical composition of the present invention is useful as the preventive or therapeutic agent for infectious diseases caused by the pathogen and their complications, e.g., viral diseases caused by influenza virus, papilloma virus, herpes virus, AIDS virus, hepatitis C virus, SARS virus, west Nile fever virus and dengue fever virus, parasite diseases caused by malaria, trypanosome and leishmania parasites, and bacterial diseases caused by bacteria, such as dysentery, enteric fever, cholera, pneumococcus, MRSA, VRE, Neisseria gonorrhoeae and Chlamydia, syphilis and tuberculosis by utilizing the actions to enhance the infection-preventing effect on the infectious antigen and reduce the infectivity titer.
By using the immunogenic foreign gene for the vertebrate other than the human being in the transfer vector for obtaining the recombinant baculovirus which is the active ingredient in the pharmaceutical composition of the present invention, it is possible to utilize the pharmaceutical composition of the present invention for procedures of the diseases associated with the infection of the target cells and the tissue as chicken influenza vaccine, bovine trypanosome vaccine and Japanese trout cold water disease vaccine by utilizing its actions to enhance the infection-preventing effect on the infectious antigen and reduce the infectivity titer.
The pharmaceutical composition of the present invention can be prepared as the composition comprising the pharmaceutically effective amount of the recombinant baculovirus and a pharmaceutically acceptable carrier.
For the infection-preventing effect of the recombinant baculovirus of the present invention in the vertebrate, particularly, the mammals including the human being or the mammalian cells, for example, the pharmaceutical composition produced by the recombinant baculovirus of the present invention and the composition capable of being added for pharmaceutical administration is administered intramuscularly, intranasally or by inhalation in the vertebrate, particularly, the mammal including the human being, which is subsequently immunized with the pharmaceutical composition comprising the recombinant baculovirus of the present invention as the active ingredient multiple times. The pharmaceutical composition of the invention is administered particularly by inhalation.
The preventive effect on the infection can be evaluated by comparing the survival rate of vertebrates administered with the recombinant baculovirus with those not administered therewith in a certain period of time after multiple immunization with the inventive pharmaceutical composition and a subsequent infection with a target pathogen.
The recombinant baculovirus, such as AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, or AcNPV-Dual-PfMSP1-PfCSP-gp64 which is the active ingredient of the pharmaceutical composition of the present invention is purified as the viral particle budded from the insect cell, comprising an expressed product of the fusion DNA sequence fusing the gene encoding the amino acid sequence of the protein capable of being the component of the viral particle to the immunogenic foreign gene of the present invention having the desired immunogenicity to enhance the preventive effect on the infection with the pathogen and exhibit the action to reduce the infectivity titer. Then, it is thought that the foreign antigen protein which became the component of the viral particle facilitates acquired immunity (humoral immunity and cellular immunity) by administering the pharmaceutical composition in the form of the viral particle to the vertebrate, particularly, the mammals including the human being, and further the antigenic protein which is the expressed product of the fusion DNA sequence further facilitates the acquired immunity (humoral immunity and cellular immunity) in the vertebrate cells, particularly, the cells in the mammals including the human being. Thus, the recombinant baculovirus of the present invention is useful as the vaccine.
In particular, the present invention provides the vaccine comprising any of the particular recombinant baculovirus such as AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, or AcNPV-Dual-PfMSP1-PfCSP-gp64 as the active ingredient.
As in the pharmaceutical composition of the above (3), the vaccine enhances infection-preventing effects against infectious antigens such as malaria antigens such as sporozoite surface antigens (CSP and TRAP) of the malaria parasite, merozoite surface membrane protein MSP1, malaria S antigen secreted from erythrocytes infected with malaria, PfEMP1 protein present in the knobs of erythrocytes infected with malaria, SERA protein, TRAMP protein, and AMA1 protein; and influenza antigens such as influenza virus HA antigen, influenza virus NA antigen, influenza virus M2 antigen, and influenza virus NP antigen; the vaccine also reduces the infectivity titer (e.g., the viral infectivity titer), thereby increasing the survival period and survival rate of mammals, including humans, compared with the group not administered with the pharmaceutical composition of the present invention. Thus, the vaccine is particularly useful as a preventive or therapeutic agent for malaria and influenza virus infection.
The vaccine of the present invention is useful as the preventive or therapeutic agent for infectious diseases caused by the pathogen and their complications, e.g., the viral diseases caused by influenza virus, papilloma virus, herpes virus, AIDS virus, hepatitis C virus, SARS virus, west Nile fever virus and dengue fever virus, the parasite diseases caused by malaria, trypanosome and leishmania parasites, and bacterial diseases caused by bacteria of dysentery, enteric fever, cholera, pneumococcus, MRSA, VRE, Neisseria gonorrhoeae and Chlamydia, syphilis and tuberculosis, by utilizing the actions to enhance the infection-preventing effect on the infectious antigen and reduce the infectivity titer.
By using the immunogenic foreign gene for the vertebrate other than the human being in the transfer vector for obtaining the recombinant baculovirus which is the active ingredient in the vaccine of the present invention, it is possible to utilize the pharmaceutical composition of the present invention for procedures of the diseases associated with the infection of the target cells and the tissue as chicken influenza vaccine, bovine trypanosome vaccine and Japanese trout cold water disease vaccine by utilizing its actions to enhance the infection-preventing effect on the infectious antigen and reduce the infectivity titer.
The recombinant baculovirus, such as AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, or AcNPV-Dual-PfMSP1-PfCSP-gp64 of the present invention, which is the active ingredient in the vaccine of the present invention, can enhance infection-preventing effects on the infectious antigen and reduces the infectivity titer, and this action or activity can be utilized for procedures of the diseases associated with the infection of the target cells or tissues. Such target cells affected by the infection include, for example blood cells, and other target cells include hepatic cells, renal cells, brain cells, lung cells, epithelial cells and muscular cells. The tissues comprising these cells include lung, liver, kidney, arterial and venous veins, stomach, intestine, urethra, skin and muscle.
The vaccine of the present invention as the pharmaceutical composition in the above (3) can be prepared as the composition comprising the pharmaceutically effective amount of the recombinant baculovirus (any one of AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-gp64, and AcNPV-Dual-PfMSP1-PfCSP-gp64) and the pharmaceutically acceptable carrier.
The vaccine can be prepared into a pharmaceutical composition form utilizing the acceptable as the pharmaceutical as with the pharmaceutical composition in the above (3) in accordance with the standard methods. The carrier can include, for example, physiologically acceptable solutions such as sterile saline and sterile buffered saline.
The vaccine (hereinafter, the formulation is the same as in the pharmaceutical composition) can be prepared as a liposome formulation comprising the recombinant baculovirus (any one of AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-00/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64) as the active ingredient, and can be combined with an adjuvant. Specific examples of the vaccine (pharmaceutical composition) of the present invention can include the liposome formulation. The liposome formulation can be one in which the recombinant baculovirus of the present invention is retained in the liposome using acidic phospholipid as a membrane component or using neutral phospholipid and acidic phospholipid as the membrane component.
The neutral phospholipid and acidic phospholipid used as the membrane component are not particularly limited, and various lipids commonly used for the liposome formulation can be used alone or in mixture of two or more.
A liposome membrane is formed in accordance with the standard methods using the acidic phospholipid alone or combining the neutral phospholipid and the acidic phospholipid. In the case of combining the neutral phospholipid, the rate of the acidic phospholipid to be combined may be about 0.1 to 100 mol %, preferably 1 to 90 mol % and more preferably about 10 to 50 mol % in the liposome membrane components.
To prepare the liposome, for example, cholesterol or the like can be added. This can control the fluidity of phospholipids and facilitates the liposome preparation. In general, the cholesterol is preferably added in an equivalent amount or less, and preferably in a 0.5-fold amount to an equivalent amount by weight, to the phospholipid.
For the rate of the active ingredient and the acidic phospholipid in the liposome formulation, the rate of the acidic phospholipid is about 0.5 to 100 equivalents, preferably about 1 to 60 equivalents and more preferably about 1.5 to 20 equivalents relative to the active ingredient.
The amount of the recombinant baculovirus of the present invention which is the active ingredient to be used can be several mol % to several tens mol %, preferably about 5 to 10 mol % and typically around 5 mol %.
The production, concentration and particle diameter control of the above liposome formulation can be performed in accordance with the standard methods. Various additives described above can also be combined with the liposome formulation if desired. Fatty acid (e.g., behenic acid, stearic acid, palmitic acid, myristic acid, oleic acid), alkyl group, cholesteryl group and the like can also be bound thereto and used. The production of the liposome formulation prepared by binding them can also be performed in accordance with the standard methods (see Long Circulating Liposomes: old drugs, New therapeutics., M. C. Woodle, G. Storm, Eds: Springer-Verlag Berlin(1998)).
The vaccine (pharmaceutical composition) of the present invention can be preferably used as a vaccine composition. When it is used, it is preferable for enhancing an anti-infection (anti-malaria or anti-influenza) effect to be combined with the adjuvant in pharmaceutically effective amount.
As the adjuvant, any ones commonly used for this type of vaccine can be used without limitation. As examples thereof, Freund's complete adjuvant, muramyl dipeptide, aluminium hydroxide, BCG, IL-12, N-acetylmuramine-L-alanyl-D-isoglutamine, thymosin α1 and QS-21 can be exemplified. The amount of the adjuvant to be combined can be appropriately determined depending on softening, erythema of skin, fever, headache and muscular pain which are likely expressed as a part of the immune response in the human beings or the animal after the administration thereof.
The vaccine (pharmaceutical composition) of the present invention can be combined with other publicly known pharmaceutical articles such as immune response-facilitating peptide and antibacterial agents (synthetic antibacterial agents).
Optional drugs and additives can be further contained in the vaccine (pharmaceutical composition). As examples thereof, the drug such as calcium ion which aids intracellular uptake of the recombinant baculovirus of the present invention can be exemplified. The drugs and additives, e.g., the liposome, and for example, fluorocarbon emulsifier, cochleate, tubule, golden particles, biodegradable microsphere and cationic polymers which make the transfection easy can be used.
The amount of the active ingredient contained in the vaccine (pharmaceutical composition) (formulation) of the present invention is not particularly limited and can be selected from the wide range as long as it is the pharmaceutically effective amount. The dosage of the vaccine (pharmaceutical composition) is not particularly limited, and can be appropriately selected from the wide range depending on the desired therapeutic effect, the administration method (administration route), the therapeutic period, age and gender of the patient, and other conditions.
When the recombinant baculovirus as an active ingredient of the vaccine (pharmaceutical composition) of the present invention is administered to a human, the recombinant baculovirus is administered in an amount corresponding to 102 to 1014 PFU, preferably 105 to 1012 PFU, and more preferably 106 to 1010 PFU per patient, calculated as the PFU of the recombinant virus.
The dosage of the recombinant baculovirus (any one of AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64) which is the active ingredient of the vaccine (pharmaceutical composition) of the present invention is selected from the very wide range as the amount of expressible DNA introduced into the vaccine host or the amount of transcribed RNA. Their amounts also depend on strength of transcription and translation promoters used for the transfer vector.
The vaccine (pharmaceutical composition) of the present invention is administered by directly injecting a recombinant baculovirus suspension in which the vector is suspended in PBS (phosphate buffered saline) or saline into a local site (e.g., in lung tissue, in liver, in muscle and in brain), inhaling through nose or airway, or administering in blood vessel (e.g., intra-arterial, intravenous, and in portal vein). The vaccine of the invention is preferably administered by inhalation.
It is preferable that the vaccine (pharmaceutical composition) of the present invention is administered not once but once to multiple times by observing the state after the initial administration and administering the additional vaccine(s). This makes it possible to enhance the desired effect. It is possible to additionally immunize with the pharmaceutical composition composed of the recombinant baculovirus (any one of AcNPV-Dual-H1N1/HA1, AcNPV-Dual-Hsp65, AcNPV-Dual-PfCSP, AcNPV-Dual-PfAMA1, AcNPV-Dual-Pfs25, AcNPV-Dual-H5N1/HA1, AcNPV-Dual-SARS/S, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39, AcNPV-CP-H1N1/NP-vp39, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-CO/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64) of the present invention after administering the vaccine (pharmaceutical composition). The combination of the above various drugs to be combined also has the possibility to enhance the therapeutic effect by the administration of the vaccine (pharmaceutical composition).
In one embodiment of the vaccine (pharmaceutical composition) of the present invention, the recombinant baculovirus which is one of the active ingredient of the vaccine (pharmaceutical composition) of the present invention can be formulated by mixing the recombinant baculovirus obtained by homologous recombination of the transfer vector in which the fusion gene obtained by fusing the desired immunogenic foreign gene and the gene encoding the protein capable of being the component of the viral particle is introduced with the baculovirus DNA in the form capable of injecting a unit dose (solution, suspension or emulsion) with the pharmaceutically acceptable carrier (i.e., non-toxic for the vertebrates including the human beings in the dosage and concentration to be administered, and compatible with other ingredients in the formulation). For example, the formulation preferably contains no antioxidant and no other compounds publicly known to be harmful for the recombinant baculovirus.
The carrier appropriately contains the additives in small amounts, such as substances which augment an isotonic property and a chemical stability. Such substances are non-toxic for the mammals including the human beings in the dosage and concentration to be administered, and can include buffers such as phosphoric acid, citric acid, succinic acid, acetic acid and other organic acids or salts thereof, antioxidants such as ascorbic acid, low molecular weight (e.g., less than about 10 residues) polypeptides (e.g., polyarginine or tripeptide) proteins (e.g., serum albumin, gelatin, or immunoglobulin), amino acids (e.g., glycine, glutamic acid, aspartic acid or arginine), monosaccharides, disaccharides and other carbohydrates (including cellulose or derivatives thereof, glucose, mannose, or dextrin), chelating agents (e.g., EDTA), sugar alcohols (e.g., mannitol or sorbitol), counterions (e.g., sodium), and/or nonionic surfactants (e.g., polysorbate, poloxamer).
The pharmaceutical vaccine (composition) comprising the recombinant baculovirus can be stored representatively in a unit or multiple dose container, e.g., a sealed ampoule or a vial as an aqueous solution or a lyophilized product.
The present invention further provides a method of preventing or treating infectious diseases caused by the pathogen and their complications, e.g., viral diseases caused by influenza virus, papilloma virus, herpes virus, AIDS virus, hepatitis C virus, SARS virus, west Nile fever virus and dengue fever virus, parasite diseases caused by malaria, trypanosome and leishmania parasites, and bacterial diseases caused by bacteria, such as dysentery, enteric fever, cholera, pneumococcus, MRSA, VRE, Neisseria gonorrhoeae and Chlamydia, syphilis and tuberculosis. The present method comprises administering an effective amount of the recombinant baculovirus, vaccine, formulation, and pharmaceutical composition of the invention to a subject. The present invention further provides a method of immunostimulation comprising administering an effective amount of the recombinant baculovirus, vaccine, formulation, and pharmaceutical composition of the invention to a subject. Examples of the subjects include those that may be infected with malaria parasites or influenza viruses, such as humans and other animals (such as mammals, birds, reptiles, fish, and amphibians), and those infected with malaria parasites or influenza viruses. The influenza virus with which the subject is infected is preferably an influenza A virus, and more preferably an influenza A subtype H1 virus, or an influenza A subtype H3 virus. Examples of malaria parasites include Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae, and Plasmodium ovale.
The recombinant baculovirus of the present invention is formed alone or together with a pharmaceutically acceptable carrier into a vaccine, formulation, or pharmaceutical composition, and administered to the subject.
The administration route may be, for example, any administration route mentioned above. The pharmaceutically acceptable carrier for use in the present invention can be suitably selected from carriers commonly used in this technical field, according to the form of the pharmaceutical composition to be produced.
For example, when the pharmacological composition is formed into an aqueous solution, purified water (sterile water) or a physiological buffer solution can be used as the carrier. When the pharmaceutical composition is formed into other appropriate solutions, organic esters capable of being injected, such as glycol, glycerol and olive oil, can be used as the carrier. The composition may contain stabilizers, excipients and the like commonly used in this technical field, and particularly in the field of vaccine formulations.
The amount of recombinant baculovirus in the vaccine, formulation, or pharmaceutical composition of the present invention is not particularly limited, and can be suitably selected from a wide range. In general, the amount of recombinant baculovirus in the composition is preferably about 0.0002 to about 0.2 (w/v %), and more preferably 0.001 to 0.1 (w/v %). The administration method of the recombinant baculovirus, vaccine, formulation, or pharmaceutical composition of the invention is not particularly limited, and can be suitably selected according to the dosage form, the patient's age, gender and other conditions, the severity of the disease, etc. A preferable dosage form thereof is a form for parenteral administration, such as injections, drops, nasal drops, and inhalants. When the composition is formed into an injection or drops, the injection can be intravenously administered as mixed with a replacement fluid such as a glucose solution or an amino acid solution as required, or can be administered intramuscularly, intracutaneously, subcutaneously or intraperitoneally.
The daily dosage of the recombinant baculovirus, vaccine, formulation, or pharmaceutical composition of the present invention may vary depending on the subject's condition, body weight, age, gender, etc., and therefore cannot be completely specified. However, the dosage is usually such that the recombinant baculovirus is administered in an amount of 0.001 to 100 mg per kg of body weight per day. The vaccine, formulation, or composition of the invention can be administered in one or more administrations per day.
When the recombinant baculovirus as an active ingredient of the vaccine (formulation or pharmaceutical composition) of the present invention is administered, the recombinant baculovirus is administered in an amount corresponding to 102 to 1014 PFU, preferably 105 to 1012 PFU, and more preferably 106 to 1010 PFU per patient, calculated as the PFU of the recombinant virus.
The vaccine (composition) of the present invention is administered according to Good Medical Practice, considering the clinical condition (for example, the condition to be prevented or treated) of each patient, the delivery site of the vaccine (composition) containing the recombinant baculovirus, the target tissue, the administration method, the dosage regimen, and other factors publicly known to those skilled in the art. Therefore, the proper dosage of the vaccine (composition) herein is determined in consideration of the above.
The present invention will be described below in more detail with reference to Examples. These Examples are exemplifications only and do not limit the present invention.
(1) Construction of Transfer Vector Plasmid pTriEx-Hsp65-gp64 of the Present Invention
(1.1) Construction of Plasmid pBACsurf-CSP
A plasmid pcDNA-CS87 was made by obtaining a NheI-NotI fragment comprising the sequence fusing genomic DNA from Plasmodium berghei ANKA strain, a signal sequence of murine Igk secretion and a FLAG sequence in accordance with Yoshida et al's method (Yoshida, S., et al., B.B.R.C., 271, 107-115 (2000) and inserting the NheI-NotI fragment in a NheI-NotI site of pcDNA3.1 (supplied from Invitrogen).
A blood sample was collected from a BALB/c mouse infected with malaria parasite P. berghei ANKA, and P. berghei genomic DNA was extracted using QIAamp DNA Midi Kit (supplied from Qiagen). Subsequently, the P. berghei ANKA genomic DNA was amplified by PCR using a primer pbCSP1: 5′-GGAGGGCTAGCATGGAGACAGACACACTCCTGCTATGGGTACTGCTGCTCTG GGTTCCAGGTTCCACTGGTGACGCGGATCCACTGCAGGACTACAAGGACGTAGACAAGGGATATG GACAAAATAAAGCATCCAAGCCC-3 (SEQ ID NO: 1) (a NheI site newly made is represented by an underline, the signal sequence of murine Igk secretion is represented by Italic and the FLAG sequence is represented by a double underline) and PbCSP-R1: GGAGGGCGGCCGCATCCCGGGTTTTCTTATTTGAACCTTTTCGTTTTCTAACTCTTATACCAGAA CC-3′ (SEQ ID NO: 2) (a NotI site newly made is represented by the underline). The PCR was performed using PfuDNA polymerase (supplied from Stratagene) by 30 cycles (denaturing at 94° C. for 30 seconds, annealing at 55° C. for one minute and extending at 72° C. for 2 minutes). The PCR product does not have glycosyl phosphatidyl inositol (GPI) anchor and encodes PbCSP fused to the signal sequence of murine Igk secretion in place of its original signal sequence.
The PCR product was purified, cleaved with restriction enzymes NheI/NotI, which was then inserted in the NheI/NotI sites of pcDNA3.1 (supplied from Invitrogen), and a resulting plasmid was designed as pcDNA-CS87. The pcDNA-CS87 plasmid contains a CMV promoter, the signal sequence of murine Igk secretion, a protein (corresponding to 21 to 299 amino acids) encoded by the PbCSP gene, a poly A signal derived from a bovine growth hormone gene and a poly A sequence.
A gene fragment encoding an amino acid sequence at positions 21 to 306 of a peptide from PbCSP was obtained by cleaving the pcDNA-CS87 with the restriction enzymes PstI and SmaI, the DNA fragment was inserted in the PstI and SmaI sites of pBACsurf (supplied from Novagen), and the constructed plasmid was designed as pBACsurf-CSP.
(1.2) Construction of Plasmid pBACsurf-Hsp65
An Hsp65 gene was obtained by extracting genomic DNA from M. tuberculosis H37Rv strain using QIAamp DNA Midi Kit (supplied from Qiagen) and cloning by PCR. That is, the genomic DNA extracted from M. tuberculosis H37Rv strain was amplified by PCR using a primer, phsp65-F1: 5′-AATAATAGATCTAATGGCCAAGACAATTGCGTACGACGAAGA-3 (SEQ ID NO: 3) (a BglII site is represented by the underline) and phsp65-R1: AATCCAATGCGGCCGCGGGAATTCGATTCCTGCAGGTCAGAAATCCATGCCACCCATGTCGCC-3 (SEQ ID NO: 4) (the NotI site is represented by the underline). The PCR product was purified, cleaved with the restriction enzymes BglII/NotI, ligated to the BamHI/NotI sites in pcDNA3.1 (supplied from Invitrogen), and the resulting plasmid was designated as pcDNA-hsp65.
The pcDNA-hsp65 plasmid is a construct in which the signal sequence of murine Igk secretion was fused to the hsp65 gene.
The PCR was performed with pcDNA-hsp65 as a template using the primer phsp65-F2: 5-CACCCCTGCAGGACTACAAGGACGACGATGACAAGGAATTCATGGCCAAGAC AATTGCGTACGACGAAGAGGCC-3′ (SEQ ID NO: 5) (Sse8387I, EcoRI sites are represented by underlines, and the FLAG sequence is represented by Italic), and phsp65-R2: (5′-CCCGGGCGAAATCCATGCCACCCATGTCGCCGCCACC-3′ (SEQ ID NO: 6) (a Cfr9I site is represented by the underline). The resulting Hsp65 gene DNA fragment (about 1660 bp) was cloned into pENTR/D-TOPO (supplied from Invitrogen), subsequently cleaved with Sse8387I/Cfr9I, which was then inserted in the PstI/Cfr9I sites of pBACsurf-CSP (Yoshida et al. Virology 316: 161-70, 2003) obtained above.
The plasmid constructed as the above was designed as pBACsurf-Hsp65.
(1.3) Construction of Plasmid pENTR-gp64
The PCR was performed with pBACgus-1 (supplied from Novagen) as the template using the primer pPolh-F2: 5′-CACCCGGACCGGATAATTAAAATGATAACCATCTCGCAAATAAATAAG-3′ (SEQ ID NO: 7) (a RsrII site is represented by the underline), and pgp64-R2: 5′-GGTACCATATTGTCTATTACGGTTTCTAATCATAC-3′ (SEQ ID NO: 8) (a KpnI site is represented by the underline). The resulting gp64 gene DNA fragment (about 1700 bp) was inserted in pENTR/D-TOPO to construct the plasmid pENTR-gp64.
The plasmid constructed as the above was designated as pENTR-gp64.
(1.4) Construction of Transfer Vector pDual-Hsp65-gp64 of the Present Invention
pDual-Hsp65-gp64 was cleaved with PstI/Cfr9I, and the hsp65 gene DNA fragment (about 1660 bp) was inserted in the PstI/Cfr9I sites of pENTR-gp64 to construct the plasmid pENTR-Hsp65-gp64.
Furthermore, pENTR-hsp65-gp64 was cleaved with RsrII/KpnI, and a DNA fragment (about 3360 bp) composed of a polyhedrin promoter and the hsp65gp64 gene was inserted in RsrII/KpnI of TriEx-3 (supplied from Novagen) to construct the transfer vector plasmid pDual-Hsp65-gp64 in which the expression was controlled by the desired dual promoters.
(2) Construction of Transfer Vector pDual-PbCSP-gp64 of the Present Invention
The plasmid pBACsurf-CSP obtained in (1.1.1) was cleaved with PstI/Cfr9I, and a PbCSP gene DNA fragment (about 890 bp) was inserted in the PstI/Cfr9I sites of pDual-Hsp65-gp64 to construct the plasmid pDual-PbCSP-gp64.
(3) Construction of Transfer Vector pDual-H1N1/HA1-gp64 of the Present Invention
RNA was extracted from a culture supernatant of MDCK cells infected with influenza virus PR8/34 strain using QIAamp MiniElute Virus Spin Kit (QIAGEN), and amplified by RT-PCR using the primer HA-f: 5′-CCTGCAGGTATGAAGGCAAACCTACTGGTC-3′ (SEQ ID NO: 9) (a SbfI site is represented by the underline) and HA-r: 5′-GCCCGGGCGATGCATATTCTGCA-3 (SEQ ID NO: 10) (a SbfI site is represented by the underline). The resulting influenza virus HA gene fragment with full length of 1700 bp was cloned into pCR-Blunt II-TOPO (supplied from Invitrogen).
The resulting plasmid was designed as pCR-Blunt-HA. The PCR was performed with the pCR-Blunt-HA as the template using the primer pHA-F1: 5′-CACCGAATTCGACACAATATGTATAGGCTACCATGCG-3′ (SEQ ID NO: 11) (an EcoRI site is represented by the underline) and pHA-R1: 5′-CCCGGGCACCTCTGGATTGGATGGACGGAATG-3′ (SEQ ID NO: 12) (a Cfr9I site is represented by the underline). The resulting H1N1/HA1 gene DNA fragment (about 1000 bp) was cloned into pENTR/D-TOPO (supplied from Invitrogen), subsequently cleaved with EcoRI/Cfr9I, which was then inserted in the EcoRI/Cfr9I sites of pDual-Hsp65-gp64 to construct the plasmid pDual-H1N1/HA1-64.
(4) Construct of Transfer Vector pDual-PbTRAMP-gp64 of the Present Invention
The blood sample was collected from a BALB/c mouse infected with malaria parasite P. berghei ANKA, and P. berghei genomic DNA was extracted using QIAamp DNA Midi Kit (supplied from Qiagen).
A PbTRAMP gene was cloned by PCR with this genomic DNA as the template according to the following method. That is, the PCR was performed using the primer pTRAMP-F1: 5′-CACCGAATTCAAAATTGATACGTGAAG-3′ (SEQ ID NO: 13) (the EcoRI site is represented by the underline) and pTRAMP-R1: CCCGGGCTTTTAATTTTGAGGAGTCTTTATTTTC-3′ (SEQ ID NO: 14) (the Cfr9I site is represented by the underline). The resulting PbTRAMP DNA fragment (about 800 bp) was cloned into pENTR/D-TOPO (supplied from Invitrogen), subsequently cleaved with EcoRI/Cfr9I, which was then inserted in the EcoRI/Cfr9I sites of pBACsurf-Hsp65. The constructed plasmid was designated as pBACsurf-PbTRAMP.
Subsequently, the pBACsurf-PbTRAMP was cleaved with EcoRI/Cfr9I, and a PbTRAMP gene DNA fragment (about 860 bp) was inserted in the EcoRI/Cfr9I sites of pDual-Hsp65-gp64 to construct the plasmid pDual-PbTRAMP-gp64.
(5) Construction of Transfer Vector pDual-PbAMA1D123-gp64 of the Present Invention
The blood sample was collected from the BALB/c mouse infected with malaria parasite P. berghei ANKA, and the P. berghei genomic DNA was extracted using QIAamp DNA Midi Kit (supplied from Qiagen).
A PbAMA1 gene domain 123 (D123) gene was cloned by PCR with this genomic DNA as the template according to the following method. That is, the PCR was performed using the primer pAMA-F1: 5′-CACCGAATTCAATCCATGGGAAAAGTATACGGAAAAATAT-3′ (SEQ ID NO: 15) (the EcoRI site is represented by the underline) and pAMA-R1: 5′-CCCGGGCTTCTCTGGTTTGATGGGCTTTCATATGCAC-3′ (SEQ ID NO: 16) (the Cfr9I site is represented by the underline). The resulting PbAMA1D123 DNA fragment (about 1280 bp) was cloned into pENTR/D-TOPO (supplied from Invitrogen), subsequently cleaved with EcoRI/Cfr9I, which was then inserted in the EcoRI/Cfr9I sites of pBACsurf-Hsp65. The constructed plasmid was designated as pBACsurf-PbAMA1D123.
Subsequently, the pBACsurf-PbAMA1D123 was cleaved with EcoRI/Cfr9I, and the PbAMA1D123 gene DNA fragment (about 1280 bp) was inserted in the EcoRI/Cfr9I sites of pDual-Hsp65-gp64 obtained in the above (1.4) to construct the plasmid pDual-PbAMA1D123-gp64.
(6) Construction of Transfer Vector pDual-PbMSP119-gp64 of the Present Invention
The blood sample was collected from the BALB/c mouse infected with malaria parasite P. berghei ANKA, and the P. berghei genomic DNA was extracted using QIAamp DNA Midi Kit (supplied from Qiagen).
A PbMSP119 gene was cloned by PCR with this genomic DNA as the template according to the following method. That is, the PCR was performed using the primer pMsp1-F1: 5′-CACCCTGCAGGACTACAAGGACGACGATGACAAGCACATAGCCTCAATAGCTTTAAATAACTTAA ATAAATCTGG-3′ (SEQ ID NO: 17) (the PstI site is represented by the underline) and pMsp1-R1: 5′-CCCGGGTTCCCATAAAGCTGGAAGAGCTACAGAATACACC-3′ (SEQ ID NO: 18) (the Cfr9I site is represented by the underline). The resulting PbMSP119 DNA fragment (about 450 bp) was cloned into pENTR/D-TOPO (supplied from Invitrogen), subsequently was cleaved with PstI/Cfr9I, which was then inserted in the PstI/Cfr9I sites of pBACsurf-Hsp65. The constructed plasmid was designated as pBACsurf-PbMSP119.
Subsequently, the pBACsurf-PbMSP119 was cleaved with PstI/Cfr9I, and the PbMSP-119 gene DNA fragment (about 450 bp) was inserted in the PstI/Cfr9I sites of pDual-Hsp65-gp64 to construct the plasmid pDual-PbMSP-1,9-gp64.
(7) Construction of Transfer Vector pDual-PfCSP-gp64 of the Present Invention
The genomic DNA of falciparum malaria parasite, P. falciparum was extracted from human erythrocytes infected with P. falciparum 3D7 strain using QIAamp DNA Midi Kit (QIAGEN). A PfCSP gene was cloned by PCR with this genomic DNA as the template according to the following method. That is, the PCR was performed using the primer pPfCSP-F1: 5′-CACCGAATTCTTATTCCAGGAATACCAGTGCTATGGAAGT-3′ (SEQ ID NO: 19) (the EcoRI site is represented by the underline) and pPfCSP-R1: 5′-CCCGGGCTTTTTCCATTTTACAAATTTTTTTTTC-3′ (SEQ ID NO: 20) (the Cfr9I site is represented by the underline). The resulting PfCSP DNA fragment (about 1100 bp) was cloned into pENTR/D-TOPO (supplied from Invitrogen), subsequently cleaved with EcoRI/Cfr9I, which was then inserted in the EcoRI/Cfr9I sites of pDual-PbAMA1D123-gp64. The constructed plasmid was designated as pDual-PfCSP-gp64.
(8) Construction of Transfer Vector pDual-PfAMA1-gp64 of the Present Invention
The genomic DNA of falciparum malaria parasite, P. falciparum was extracted from human erythrocytes infected with P. falciparum 3D7 strain using QIAamp DNA Midi Kit (QIAGEN). The PfAMA1 gene was cloned by PCR with this genomic DNA as the template according to the following method. That is, the PCR was performed using the primer pPfAMA1-F1: 5′-CACCCTGCAGGACTACAAGGACGACGATGACAAGCAGAATTATTGGGAACATCCATAT CAAAATAGTGATGTG-3′ (SEQ ID NO: 21) (the PstI site is represented by the underline, the FLAG sequence represented by Italic) and pPfAMA1-R1: 5′-CCCGGGCTTTCATTTTATCATAAGTTGGTTTATG-3′ (SEQ ID NO: 22) (the Cfr9I site is represented by the underline). The resulting PfAMA1 DNA fragment (about 3500 bp) was cloned into pENTR/D-TOPO (supplied from Invitrogen), subsequently cleaved with PstI/Cfr9I, which was then inserted in the PstI/Cfr9I sites of PbAMA1D123-gp64. The constructed plasmid was designated as pDual-PfAMA1-gp64.
(9) Construction of Transfer Vector pDual-Pfs25-gp64 of the Present Invention
The genomic DNA of falciparum malaria parasite, P. falciparum was extracted from human erythrocytes infected with P. falciparum 3D7 strain using QIAamp DNA Midi Kit (QIAGEN). The Pfs25 gene was cloned by PCR with this genomic DNA as the template according to the following method. That is, the PCR was performed using the primer pPfs25-F1: 5′-CACCGAATTCAAAGTTACCGTGGATACTGTATGCAAAAGAGGA-3′ (SEQ ID NO: 23) (the EcoRI site is represented by the underline), and pPfs25-R1: 5′-CCCGGGCAGTACATATAGAGCTTTCATTATCTAT-3′ (SEQ ID NO: 24) (the Cfr9I site is represented by the underline). The resulting Pfs25 DNA fragment (about 530 bp) was cloned into pENTR/D-TOPO (supplied from Invitrogen), subsequently cleaved with EcoRI/Cfr9I, which was then inserted in the EcoRI/Cfr9I sites of PbAMA1D123-gp64. The constructed plasmid was designated as pDual-Pfs25-gp64.
(10) Construction of Transfer Vector pDual-H5N1/HA1-gp64 of the Present Invention
An HA1 gene is synthesized from bird influenza virus H5N1, and inserted in the EcoRI/Cfr9I sites of pDual-Hsp65-gp64 to construct the plasmid pDual-H5N1/HA1-gp64.
(11) Construction of Transfer Vector pDual-SARS/S-gp64 of the Present Invention
An S gene of SARS virus is synthesized and inserted in the EcoRI/Cfr9I sites of pDual-Hsp65-gp64 to construct the plasmid pDual-SARS/S-gp64.
(12) Construction of Transfer Vector pCP-H1N1/HA1-gp64 of the Present Invention
The PCR was performed with pCR-Blunt-HA as the template using Polh-f RsrII (5′-GGGCGGACCGGATAATTAAAATGATAACCATCTCG-3′: SEQ ID NO: 25) (the RsrII site is represented by the underline) and GP64-r DraIII (5′-GGGCACTTAGTGATATTGTCTATTACGGTTTCTAATC-3′: SEQ ID NO: 26) (the DraIII site is represented by the underline). A resulting DNA fragment of 2700 bp was linked to a vector obtained by digesting pDual-H1N1/HA1-gp64 with the restriction enzymes RsrII and DraIII to construct pCP-H1N1/HA1-gp64.
(13) Construction of Transfer Vector pCAP-H1N1/HA1-gp64 of the Present Invention
HA1 obtained by cleaving pCP-H1N1/HA1-gp64 with the restriction enzymes RsrII and DraIII and a gp64 gene fragment were inserted in the vector obtained by cleaving pTriEx-1.1 (supplied from Novagen) with the restriction enzymes RsrII and DraIII to construct a plasmid pCAP-H1N1/HA1-gp64.
(14) Construction of Transfer Vector pCU-H1N1/HA1-gp64 of the Present Invention
The PCR was performed with pTriEx3.1 as the template using CMVenh-f FseI (5′-GGGGGCCGGCCCTAGTTATTAATAGTAATCAATTAC-3′: SEQ ID NO: 27) (the FseI site is represented by the underline) and CMVenh-r KpnI (5′-GGGGGTACCCATGGTAATAGCGATG ACTAATACG-3′: SEQ ID NO: 28) (the KpnI site is represented by the underline) to amplify a CMV enhancer region. In addition, the PCR was performed with human genomic DNA as the template using UBBp-f KpnI (5′-GGGGGTACCTCGAGGAAGGTTTCTTCAACTC-3′: SEQ ID NO: 29) (the KpnI site is represented by the underline) and UBBp-r RsrII (5′-GGGCGGTCCGGACCTAGTTTAAAAGTAAAACATAAG-3′: SEQ ID NO: 30) (the RsrII site is represented by the underline) to amplify an UBB promoter region. Resulting two fragments were linked to the vector obtained by digesting pCP-H1N1/HA1-gp64 with the restriction enzymes FseI and RsrII to construct pCU-H1N1/HA1-gp64.
(15) Construction of Transfer Vector pDual-H1N1/NP-gp64 of the Present Invention
The RT-PCR was performed with genomic RNA from influenza virus PR8/34 strain as the template using NP-f EcoRI (5′-ACGGAATTCCATTCAATTCAAACTGGA-3′: SEQ ID NO: 31 (the EcoRI site is represented by the underline) and NP-r Cfr9I (5′-GATCCCGGGCCTTGTCAATGCTGAATGGCAA-3′: SEQ ID NO: 32) (the Cfr9I site is represented by the underline). A resulting fragment was digested with the restriction enzymes EcoRI and Cfr9I, and inserted in pCP-H1N1/HA1-gp64 digested with the restriction enzymes EcoRI and Cfr9I to make pDual-H1N1/NAe-gp64.
(16) Construction of Transfer Vector pDual-H1N1/M2-gp64 of the Present Invention
The RT-PCR was performed with genomic RNA from influenza virus PR8/34 strain as the template using M2-f EcoRI (5′-CGGAATTCATGAGTCTTCTAACCGAGG-3′: SEQ ID NO: 33) (the EcoRI site is represented by the underline) and M2-r Cfr9I (5′-GATCCCGGGCCTCCAGCTCTATGCTGAC-3′: SEQ ID NO: 34) (the Cfr9I site is represented by the underline). A resulting fragment was digested with the restriction enzymes EcoRI and Cfr9I, and inserted in pCP-H1N1/HA1-gp64 digested with the restriction enzymes EcoRI and Cfr9I to make pDual-H1N1/M2-gp64.
(17) Construction of Transfer Vector pDual-H1N1/NAe-gp64 of the Present Invention
The RT-PCR was performed with genomic RNA from influenza virus PR8/34 strain as the template using NAe-f EcoRI (5′-ACGGAATTCCATTCAATTCAAACTGGA-3′: SEQ ID NO: 35) (the EcoRI site is represented by the underline) and NAe-r Cfr9I (5′-GATCCCGGGCCTTGTCAATGCTGAATGGCAA-3′: SEQ ID NO: 36) (the Cfr9I site is represented by the underline). A resulting fragment was digested with the restriction enzymes EcoRI and Cfr9I, and inserted in pCP-H1N1/HA1-gp64 digested with the restriction enzymes EcoRI and Cfr9I to make pDual-H1N1/NAe-gp64.
(18) Construction of Transfer Vector pDual-M2e-gp64 of the Present Invention
The PCR was performed with pDual-H1N1/M2-gp64 as the template using M2-f EcoRI (5′-CGGAATTCATGAGTCTTCTAACCGAGG-3′: SEQ ID NO: 37) (the EcoRI site is represented by the underline) and M2e-r Cfr9I (5′-GATCCCGGGCATCACTTGAACCGTTGCA-3′: SEQ ID NO: 38) (the Cfr9I site is represented by the underline). A resulting fragment was digested with the restriction enzymes EcoRI and Cfr9I, and inserted in pCP-H1N1/HA1-gp64 digested with the restriction enzymes EcoRI and Cfr9I to make pDual-M2e-gp64.
(19) Construction of Transfer Vector pCP-HA1/NC99-gp64 of the Present Invention
RNA was extracted from a frozen stock of influenza virus NewCaledonia99/20 (NC99) using QIAamp MiniElute Virus Spin Kit (QIAGEN), and the RT-PCR was performed using HA1-f EcoRI(5′-GATGAATTCGACACAATATGTATAGGCTACC-3′: SEQ ID NO:39) (the EcoRI site is represented by the underline) and HA1-r CFr9I (NC99) (5′-GATCCCGGGCTCTGGATTGAATGGATGGGATG-3′: SEQ ID NO:40) (the Cfr9I site is represented by the underline) to amplify an HA1 gene fragment. A resulting fragment and pCP-H1N1/HA1-gp64 were treated with the restriction enzymes EcoRI and Cfr9I to newly insert the HA1 gene fragment derived from NC99 in an HA1 introduction region of pCP-H1N1/HA1-gp64. A resulting plasmid was designated as pCP-HA1/NC99-64.
(20) Construction of Transfer Vector pCP-H1N1/HA0-gp64 of the Present Invention
The PCR was performed with pCR-Blunt-HA as the template using HA0-f EcoRI (5′-GGGGAATTCATGAAGGCAAACCTACTGG-3′: SEQ ID NO: 41) (the EcoRI site is represented by the underline) and HA2-r Cfr9I (5′-GATCCCGGGCGATGCATATTCTGCA-3′: SEQ ID NO: 42) (the Cfr9I site is represented by the underline) to amplify the full length HA gene. A resulting fragment and pCP-H1N1/HA1-gp64 were treated with the restriction enzymes EcoRI and Cfr9I to newly insert the HA0 gene fragment in the HA1 introduction region of pCP-H1N1/HA1-gp64. A resulting plasmid was designated as pCP-H1N1/HA0-gp64.
(21) Construction of Transfer Vector pCP-H1N1/HA2-gp64 of the Present Invention
The PCR was performed with pCR-Blunt-HA as the template using HA2-f EcoRI (5′-GATGAATTCATATTTGGAGCCATTGCCG-3′: SEQ ID NO: 43) (the EcoRI site is represented by the underline) and HA2-r Cfr9I (5′-GATCCCGGGCGATGCATATTCTGCA-3′: SEQ ID NO: 44) (the Cfr9I site is represented by the underline) to amplify the full length HA gene. A resulting fragment and pCP-H1N1/HA1-gp64 were treated with the restriction enzymes EcoRI and Cfr9I to newly insert the HA2 gene fragment in the HA1 introduction region of pCP-H1N1/HA1-gp64. A resulting plasmid was designated as pCP-H1N1/HA2-gp64.
(22) Construction of Transfer Vector pCP-H1N1/HA1-vp39 of the Present Invention
The PCR was performed with baculovirus DNA attached to BacVector-2000 Transfection Kit (Novagen) as the template using vp39-f (5′-CTTACTAGTATGGACTACAAGGACGACGATGACAAGGAATTCGG CGGCGGCGGCTCGGCGCTAGTGCCCGTGGGT-3′: SEQ ID NO: 45) (the SpeI site is represented by the underline and the EcoRI site is represented by the double underline) and vp39-r (5′-CTT CACTTAGTGATGGTGATGATGGTGGTGCCCGGGGCTTTAAAGCTTGACGGCTATTCCTCCACC-3′: SEQ ID NO: 46) (the DraIII site is represented by the underline and the SmaI is represented by the double underline) to amplify a vp39 gene region. An amplified fragment and pDual-H1N1/HA1-gp64 were cleaved with the restriction enzymes SpeI and DraIII, and ligated one another to construct pDual-vp39. Furthermore, the PCR was performed with pDual-H1N1/HA1-gp64 as the template using Polh-S1 (5′ GCTAACCATGTTCATGCC-3′: SEQ ID NO: 47) and HA1-r EcoRI (5′-GGGGAATTCACCTCTGGATTGGAT GGAC-3′: SEQ ID NO: 48) (the EcoRI site is represented by the underline). A resulting fragment was digested with EcoRI to prepare the HA1 gene. A resulting fragment was inserted in pDual-vp39 digested with EcoRI to construct pCP-H1N1/HA1-vp39.
(23) Construction of Transfer Vector pCP-H1N1/NP-vp39 of the Present Invention
The PCR was performed with pDual-H1N1/NP-gp64 as the template using NP-f 5 EcoRI (5′-ACGGAATTCATGGCGTCCCAAGGCACC-3′: SEQ ID NO: 49) (the EcoRI site is represented by the underline) and NP-r EcoRI (5′-ACGGAATTCATTGTCGTACTCCTCTGCATTG-3′: SEQ ID NO: 50) (the EcoRI site is represented by the underline). A resulting fragment was digested with EcoRI. A resulting fragment was inserted in pDual-vp39 digested with EcoRI to construct pCP1-H1N1/NP-vp39.
(1.1) Construction of pcDNA-GL3 (luc)
pGL3-Enhancer (Promega) was cleaved with the restriction enzymes HindIII/XbaI, a luciferase gene DNA fragment (about 1690 bp) was ligated to the HindIII/XbaI sites of pcDNA3.1 (supplied from Invitrogen), and the resulting plasmid was designated as pcDNA-GL3(luc).
(1.2) Construct of pBACgus-CMV-IgHsp65 pcDNA-hsp65 obtained in the above Example 1 (1.2) was cleaved with the restriction enzymes BamHI/NotI, and inserted in the BamHI/NotI sites to produce pcDNA-Ighsp65. The resulting plasmid was designated as pcDNA-IgHsp65.
Subsequently, the pcDNA-IgHsp65 was cleaved with BglII/SphI, and a gene cassette (about 2850 bp) composed of the CMV promoter, the Hsp65 gene carrying the murine Igk signal sequence, and the poly A signal derived from the bovine growth hormone was inserted in the BglII/SphI sites of pBACgus-1 (Novagen). The constructed plasmid was designated as pBACgus-CMV-Hsp65.
(1.3) Construction of pBACgus-CMV-GL3
The plasmid pcDNA-GL3(luc) obtained above was cleaved with the restriction enzymes NheI/XbaI, the luciferase gene DNA fragment (about 1690 bp) was inserted in the NheI/XbaI sites of the plasmid pBACgus-CMV-Hsp65, and the resulting plasmid was designated as pBACgus-CMV-GL3.
(1.4) Construction of pBACgus-CMV-PbCSP
A gene fragment encoding the amino acid sequence corresponding to positions 21 to 306 of the PbCSP peptide was yielded by cleaving the plasmid pBACsurf-CSP with the restriction enzymes PstI and SmaI, the DNA fragment (about 858 bp) was inserted in the PstI and SmaI sites of pBACgus-CMV-GL3 obtained above, and the resulting plasmid was designated as pBACgus-CMV-PbCSP.
(1.5) Construction of pBACgus-CMV-HA-full
pCR-Blunt-HA was cleaved with BamHI/Sse83871, and an HA gene DNA fragment (about 1750 bp) was inserted in the BamHI/PstI site of pBluescript II (KS-) to construct the plasmid pBluescript-HA.
Furthermore, the pBluescript-HA was cleaved with HindIII/XbaI, and an HA gene DNA fragment (about 1800 bp) was inserted in the HindIII/XbaI sites of pBACgus-CMV-GL3 obtained in (1.3) to construct the plasmid pBACgus-CMV-HA-full.
(1) Construction of Transfer Vector Plasmids pCAP-PfCSP, pCAP-PfCSP/272, and pCAP-PfCSP/467 of the Present Invention
(1.1) Construction of Plasmid pBACsurf-Hsp65
An Hsp65 gene was obtained by extracting genomic DNA from M. tuberculosis H37Rv strain using a QIAamp DNA Midi Kit (Qiagen), and cloning by PCR. More specifically, the genomic DNA extracted from the M. tuberculosis H37Rv strain was amplified by PCR using primers phsp65-F1 (5′-AATAATAGATCTAATGGCCAAGACAATTGCGTACGACGAAGA-3′ (SEQ ID NO: 3); the BglII site is underlined) and phsp65-R1 (5′-AATCCAATGCGGCCGCGGGAATTCGATTCCTGCAGGTCAGAAATCCATGCCACCCATGTCGCC-3′ (SEQ ID NO: 4); the NotI site is underlined). The PCR product was purified, cleaved with restriction enzymes BglII and NotI, ligated to pcDNA3.1(+) (from Invitrogen) digested with BamHI and NotI. The resulting plasmid was designated pcDNA-hsp65. PCR was performed with pcDNA-hsp65 as a template using primers phsp65-F2 (5′-CACCCCTGCAGGACTACAAGGACGACGATGACAAGGAATTCATGGCCAAGAC AATTGCGTACGACGAAGAGGCC-3′ (SEQ ID NO: 5); the Sse8387I and EcoRI sites are underlined, and the FLAG sequence is italicized), and phsp65-R2 (5′-CCCGGGCGAAATCCATGCCACCCATGTCGCCGCCACC-3′ (SEQ ID NO: 6); the Cfr9I site is underlined). The resulting Hsp65 gene DNA fragment was cloned into pENTR/D-TOPO (from Invitrogen), then cleaved with Sse83871/Cfr9I and inserted into the PstI/Cfr9I site of pBACsurf-CSP (Yoshida et al., Virology 316: 161-70, 2003). The plasmid thus constructed was designed pBACsurf-Hsp65.
(1.2) Construction of Plasmid pENTR-gp64
PCR was performed with pBACsurf-1 (from Novagen) as a template using primers pPolh-F2 (5′-CACCCGGACCGGATAATTAAAATGATAACCATCTCGCAAATAAATAAG-3′ (SEQ ID NO: 7); the RsrII site is underlined), and pgp64-R2 (5′-GGTACCATATTGTCTATTACGGTTTCTAATCATAC-3′ (SEQ ID NO: 8); the KpnI site is underlined). The resulting gp64 gene DNA fragment was inserted into pENTR/D-TOPO to construct a plasmid pENTR-gp64. The plasmid thus constructed was designated pENTR-gp64.
(1.3) Construction of Transfer Vector pDual-Hsp65-gp64 of the Present Invention
pBACsurf-Hsp65 was cleaved with PstI/Cfr9I, and the hsp65 gene DNA fragment was inserted into the PstI/Cfr9I site of pENTR-gp64 to construct a plasmid pENTR-Hsp65-gp64. The pENTR-Hsp65-gp64 was cleaved with RsrII/KpnI, and a DNA fragment consisting of a polyhedrin promoter and hsp65-gp64 gene was inserted into pTriEx-3.1 (Novagen) cleaved with RsrII and KpnI to construct a transfer vector plasmid pDual-Hsp65-gp64 enabling the expression of a fusion protein of Hsp65 antigen and gp64 protein in mammalian and insect cells under the control of the desired dual promoter consisting of CMA promoter and polyhedrin promoter.
(1.4) Construction of Transfer Vector pDual-H1N1/HA1-gp64 of the Present Invention
RNA was extracted from a culture supernatant of MDCK cells infected with influenza virus PR/8/34 strain using a QIAamp MinElute Virus Spin Kit (from Qiagen), and amplified by RT-PCR using primers HA-f (5′-CCTGCAGGTATGAAGGCAAACCTACTGGTC-3′ (SEQ ID NO: 9); the SbfI site is underlined) and HA-r (5′-GCCCGGGCGATGCATATTCTGCA-3 (SEQ ID NO: 10); the SbfI site is underlined). The resulting influenza virus HA gene fragment was cloned into pCR-Blunt II-TOPO (from Invitrogen). The resulting plasmid was designated as pCR-Blunt-HA. PCR was performed with the pCR-Blunt-HA as a template using primers pHA-F1 (5′-CACCGAATTCGACACAATATGTATAGGCTACCATGCG-3′ (SEQ ID NO: 11); the EcoRI site is underlined) and pHA-R1 (5′-CCCGGGCACCTCTGGATTGGATGGACGGAATG-3′ (SEQ ID NO: 12); the Cfr9I site is underlined). The resulting H1N1/HA1 gene DNA fragment was cloned into pENTR/D-TOPO, then cleaved with EcoRI/Cfr9I and inserted into the EcoRI/Cfr9I site of pDual-Hsp65-gp64 to construct a plasmid pDual-H1N1/HA1-gp64.
(1.5) Construction of Plasmid pBACsurf-HA1
pDual-H1N1/HA1-gp64 was cleaved with EcoRI/CfrI, and the DNA fragment of H1N1/HA1 gene was inserted into pBACsurf-Hsp65 digested with EcoRI and CfrI to construct a plasmid pBACsurf-HA1.
(1.6) Construction of Plasmid pCP-H1N1/HA1-64
PCR was performed with pBACsurf-HA1 as a template using Polh-f RsrII (5′-GGGCGGACCGGATAATTAAAATGATAACCATCTCG-3′ (SEQ ID NO: 25); the RsrII site is underlined) and GP64-r DraIII (5′-GGGCACTTAGTGATATTGTCTATTACGGTTTCTAATC-3′ (SEQ ID NO: 26); the DraIII site is underlined). The resulting DNA fragment was inserted into pDual-H1N1/HA1-gp64 digested with RsrII and DraIII to yield pCP-H1N1/HA1-gp64.
(1.7) Construction of Plasmid pCAP-H1N1/HA1-gp64
pCP-H1N1/HA1-gp64 was cleaved with restriction enzymes RsrII and DraIII to prepare HA1 and gp64 gene fragments. The fragments were inserted into a vector prepared by digesting pTriEx-1.1 (from Novagen) with restriction enzymes RsrII and DraIII to yield a transfer vector plasmid pCAP-H1N1/HA1-gp64 enabling the expression of a fusion protein of HA1 antigen and gp64 protein in mammalian and insect cells under the control of the desired dual promoter consisting of CAG promoter and polyhedrin promoter.
(1.8) Construction of Plasmid pCAP-H1N1/NP-64
RT-PCR was performed with genomic RNA of influenza virus PR/8/34 strain as a template using NP-f EcoRI (5′-ACGGAATTCCATTCAATTCAAACTGGA-3′ (SEQ ID NO: 31); the EcoRI site is underlined) and NP-r Cfr9I (5′-GATCCCGGGCCTTGTCAATGCTGAATGGCAA-3′ (SEQ ID NO: 32); the Cfr9I site is underlined). The obtained fragments were digested with restriction enzymes EcoRI and Cfr9I, and inserted into pCAP-H1N1/HA1-gp64 digested with restriction enzymes EcoRI and Cfr9I to yield pCAP-H1N1/NP-gp64.
(1.9) Construction of Plasmids pCAP-H1N1/NP/272 and pCAP-H1N1/NP/467
PCR was performed using gp64 (272)-f (5′-GACTCCCCGGGTCGAGCACCGAGTCAAGAAG-3′ (SEQ ID NO: 51); the XmaI site is underlined), gp64 (467)-f (5′-GACTCCCCGGGACATCACTTCCATGGCTGAA-3′ (SEQ ID NO: 52); the XmaI site is underlined), and GP64-r DraIII (5′-GGGCACTTAGTGATATTGTCTATTACGGTTTCTAATC-3′ (SEQ ID NO: 26); the DraIII site is underlined) of pCAP-H1N1/HA1-gp64. The obtained fragments were digested with restriction enzymes XmaI and DraIII, and inserted into pCAP-H1N1/NP-gp64 digested with XmaI and DraIII to yield pCAP-H1N1/NP/272 and pCAP-H1N1/NP/467.
(1.10) Construct of Transfer Vectors pCAP-PfCSP, cCAP-PfCSP/272 and pCAP-PfCSP/467 of the Present Invention
P. falciparum genomic DNA was extracted from human erythrocytes infected with Plasmodium falciparum 3D7 strain using a QIAamp DNA Midi Kit (from Qiagen). A PfCSP gene was cloned by PCR with this genomic DNA as a template according to the following method. The PCR was performed using primers PfCSP-f (19) (5′-GACTCTGCAGTTATTCCAGGAATACCAGTGCTATGGAAG-3′ (SEQ ID NO: 53); the PstI site is underlined) and PfCSP-r (373) (5′-CGATCCCGGGCTTTTTCCATTTTACAAATTTTTTTTTCAATATC-3′ (SEQ ID NO: 54); the XmaI site is underlined). The resulting DNA fragment was inserted into pCAP-H1N1/NP-gp64, pCAP-H1N1/NP/272, and pCAP-H1N1/NP/467, each digested with PstI and XmaI. The constructed plasmids were designated pCAP-PfCSP, pCAP-PfCSP/272, and pCAP-PfCSP/467.
The GenBank accession number of the amino acid sequence of the Plasmodium falciparum 3D7 circumporozoite (CS) protein is XP—001351122.
(2) Construction of Transfer Vector pDual-Pfs25-PfCSP-gp64 of the Present Invention
(2.1) Construction of Plasmid pDual-PbAMA1D123-gp64
A blood sample was collected from a BALB/c mouse infected with malaria parasite P. berghei ANKA strain, and P. berghei genomic DNA was extracted using a QIAamp DNA Midi Kit (Qiagen). A PbAMA1 gene domain 123 (D123) was cloned by PCR with this genomic DNA as a template according to the following method. PCR was performed using primers pAMA-F1 (5′-CACCGAATTCAATCCATGGGAAAAGTATACGGAAAAATAT-3′ (SEQ ID NO: 15); the EcoRI site is underlined) and pAMA1-R1 (5′-CCCGGGCTTCTCTGGTTTGATGGGCTTTCATATGCAC-3′ (SEQ ID NO: 16); the Cfr9I site is underlined). The resulting PbAMA1D123 DNA fragment was cloned into pENTR/D-TOPO, then cleaved with EcoRI/Cfr9I and inserted into pBACsurf-Hsp65 digested with EcoRI and Cfr9I. The constructed plasmid was designated pBACsurf-PbAMA1D123.
Subsequently, the pBACsurf-PbAMA1D123 was cleaved with EcoRI/Cfr9I, and the PbAMA1D123 gene DNA fragment was inserted into pDual-Hsp65-gp64 digested with EcoRI and Cfr9I to yield a plasmid pDual-PbAMA1D123-gp64.
(2.2) Construction of Plasmid pDual-PfCSP-gp64
A PfCSP gene was cloned by PCR with P. falciparum genomic DNA as a template according to the following method. The PCR was performed using primers pPfCSP-F1 (5′-CACCGAATTCTTATTCCAGGAATACCAGTGCTATGGAAGT-3′ (SEQ ID NO: 19); the EcoRI site is underlined) and pPfCSP-R1 (5′-CCCGGGCTTTTTCCATTTTACAAATTTTTTTTTC-3′ (SEQ ID NO: 20); the Cfr9I site is underlined). The resulting PfCSP DNA fragment was cloned into pENTR/D-TOPO, then cleaved with EcoRI/Cfr9I and inserted into pDual-PbAMA1D123-gp64 digested with EcoRI and Cfr9I. The constructed plasmid was designated pDual-PfCSP-gp64.
(2.3) Construction of Transfer Vector pDual-Pfs25-PfCSP-gp64 of the Present Invention
A Pfs25 gene was cloned by PCR with P. falciparum genomic DNA as a template according to the following method. The PCR was performed using primers pPfs25-F1 (5′-CACCGAATTCAAAGTTACCGTGGATACTGTATGCAAAAGAGGA-3′ (SEQ ID NO: 23); the EcoRI site is underlined) and pPfs25-R2 (5′-CAATTGAGATCCGCCGCCACCGCCACCAGTACATATAGAGCTTTCATTATCTATTATAAATCCAT C-3′ (SEQ ID NO: 55); the MunI site is underlined). The resulting Pfs25 DNA fragment was cloned into pENTR/D-TOPO, then cleaved with EcoRI/MunI, and inserted into pDual-PfCSP-gp64 digested with EcoRI. The constructed plasmid was designated pDual-Pfs25-PfCSP-gp64.
(3) Construction of Transfer Plasmid pDual-PfMSP1-PfCSP-gp64 of the Present Invention
A PfMSP1 gene was cloned by PCR with P. falciparum genomic DNA as a template according to the following method. The PCR was performed using primers pPfMSP119-F1 (5′-CACCGAATTCAACATTTCACAACACCAATGCGTAAAAAAAC-3′: (SEQ ID NO: 56); the EcoRI site is underlined) and pPfMSP119-R2 (5′-CAATTGAGATCCGCCGCCACCGCCACCGTTAGAGGAACTGCAGAAAATACCATCGAAAAGTGGA-3′ (SEQ ID NO: 57); the MunI site is underlined). The resulting PfMSP119 DNA fragment was cloned into pENTR/D-TOPO, then cleaved with EcoRI and MunI, and inserted into pDual-PbCSP-gp64 digested with EcoRI. The constructed plasmid was designated pDual-PfMSP1-PfCSP-gp64.
(4) Construction of the Transfer Vector Plasmids pCAP-PfCSP (A361E), pCAP-PfCSP(A361E)/272, and pCAP-PfCSP(A361E)/467 of the Present Invention
PCR was performed with pCAP-PfCSP using PfCSP-f (19) (5′-GACTCTGCAGTTATTCCAGGAATACCAGTGCTATGGAAG-3′: (SEQ ID NO: 53); the PstI site is underlined) and PfCSP-r (373 A361E) (5′-CGATCCCGGGCTTTTTCCATTTTACAAATTTTTTTTTCAATATCATTTTC-3′: (SEQ ID NO: 58); the XmaI site is underlined). The obtained DNA fragment was cleaved with PstI and XmaI, and inserted into pCAP-H1N1/NP-gp64, pCAP-H1N1/NP/272, and pCAP-H1N1/NP/467, each digested with PstI and XmaI. The constructed plasmids were designated pCAP-PfCSP (A361E), pCAP-PfCSP (A361E)/272, and pCAP-PfCSP (A361E)/467.
(5) Construction of Transfer Plasmids pCAP-PfCSP-76 and pCAP-PfCSP-76/467 of the Present Invention
PCR was performed with pCAP-PfCSP (A361E) using PfCSP-f (76) (5′-GACTCTGCAGGATGATGGAAATAACGAAGACAACG-3′: (SEQ ID NO: 59); the PstI site is underlined) and PfCSP-r (373 A361E) (5′-CGATCCCGGGCTTTTTCCATTTTACAAATTTTTTTTTCAATATCATTTTC-3′: (SEQ ID NO: 58); the XmaI site is underlined). The resulting DNA fragment was cleaved with PstI and XmaI, and then inserted into pCAP-H1N1/NP-gp64 and pCAP-H1N1/NP/467, each cleaved with PstI and XmaI. The constructed plasmids were designated pCAP-PfCSP-76 and pCAP-PfCSP-76/467.
(6) Construction of Transfer Plasmids pCAP-PfCSP+209 and pCAP-PfCSP+209/467
An artificial gene sequence (PfCSP+: SEQ ID NO: 60) was prepared from the amino acid sequence of PfCSP of P. falciparum 3D7 strain (in which, however, the A at the 361-position was replaced by E) using codons frequently used in Sf9 and human cells. Using the obtained artificial gene sequence as a template, PCR was performed using PfCSP-f(+209) (5′-GACTCTGCAGAACGCTAATCCAAACGCTAATCCCAACGCTAATCCCAATGCC-3′ (SEQ ID NO: 61); the PstI site is underlined) and PfCSP-r(+A361E) (5′-CGATCCCGGGCTTTTTCCATTTTGCAAATTTTTTT-3′ (SEQ ID NO: 62); the XmaI site is underlined). The resulting DNA fragments were cleaved with PstI and XmaII, and then inserted into pCAP-H1N1/NP-gp64 and pCAP-H1N1/NP/467 digested with PstI and XmaII. The constructed plasmids were designated pCAP-PfCSP+209 and pCAP-PfCSP+209/467.
(7) Construction of Transfer Plasmids pCAP-PfCSP+76/209 and pCAP-PfCSP+76/209/467 of the Present Invention
Using the artificial gene sequence (PfCSP+: SEQ ID NO: 60) as a template, PCR was performed using PfCSP-f(+76) (5′-GACTCTGCAGGACGACGGCAACAACGAAGACAACG-3′ (SEQ ID NO: 63); the PstI site is underlined), PfCSP-r(+128) (5′-CGTTAGGATCCACATTTGGGTTGGCATTTGGG-3′ (SEQ ID NO: 64); the BamHI site is underlined), PfCSP-f (+209) BamHI (5′-GACTGGATCCTAACGCTAATCCAAACGCTAATCCC-3′: (SEQ ID NO: 65); the BamH I site is underlined), and PfCSP-r(+A361E) (5′-CGATCCCGGGCTTTTTCCATTTTGCAAATTTTTTT-3′ (SEQ ID NO: 62); the XmaI site is underlined) from the obtained artificial gene sequence. The resulting DNA fragments were cleaved with PstI/BamHI and BamHl/XmaI, respectively, and then inserted into pCAP-H1N1/NP-gp64 and pCAP-H1N1/NP/467, each digested with PstI and XmaI. The constructed plasmids were designated pCAP-PfCSP+76/209 and pCAP-PfCSP+76/209/467.
(8) Construction of Transfer Plasmids pCAP-HA1/Anhui, pCAP-HA1/Anhui/272, and pCAP-HA1/Anhui/467
An artificial gene sequence (SEQ ID NO: 66) was prepared from the amino acid sequence of the hemagglutinin region of influenza virus H5N1/Anhui/1/05 using codons frequently used in Sf9 and human cells. Using the obtained artificial gene sequence as a template, PCR was performed using AH-F1 (5′-CAGTCTGCAGGACCAGATTTGCATC-3′: (SEQ ID NO: 67); the PstI site is underlined) and AH-R4 (5′-CAGTCCCGGGCTCTCTTGCGCCTGC-3′: (SEQ ID NO: 68); the XmaI site is underlined). The obtained DNA fragment was cleaved with PstI and XmaI, and then inserted into pCAP-H1N1/NP-gp64, pCAP-H1N1/NP/272 and pCAP-H1N1/NP/467, each digested with PstI and XmaI. The constructed plasmids were designated pCAP-HA1/Anhui, pCAP-HA1/Anhui/272, and pCAP-HA1/Anhui/467.
The GenBank accession number of the amino acid sequence of the hemagglutinin of influenza virus A/H5N1/Anhui/1/05 is ABD28180.
(9) Construction of Transfer Vector Plasmids pCAP-HA1/Vietnam, pCAP-HA1/Vietnam/51, pCAP-HA1/Vietnam/101, pCAP-HA1/Vietnam/154, pCAP-HA1/Vietnam/201, pCAP-HA1/Vietnam/272, and pCAP-HA1/Vietnam/467 of the Present Invention
An artificial gene sequence (SEQ ID NO: 69) was prepared from the amino acid sequence of the HA1 region of the hemagglutinin of influenza virus H5N1/Vietnam/1203/4 using codons frequently used in Sf9 and human cells. Using the obtained artificial gene sequence as a template, PCR was performed using VN-F1 (5′-CAGTCTGCAGGACCAGATCTGTATC-3′: (SEQ ID NO: 70); the PstI site is underlined), and VN-R4 (5′-CAGTCCCGGGCTCTCTTCTTCCTGC-3′: (SEQ ID NO: 71); the XmaI site is underlined). The obtained DNA fragment was cleaved with PstI and XmaI, and inserted into pCAP-H1N1/NP-gp64, pCAP-H1N1/NP/272 and pCAP-H1N1/NP/467, each digested with PstI and XmaI. The constructed plasmids were designated pCAP-HA1/Vietnam, pCAP-HA1/Vietnam/272, and pCAP-HA1/Vietnam/467.
Further, using pCAP-HA1/Vietnam as a template, PCR was performed using primers gp64(51)-f (5′-GACTCCCCGGGTGGAAATCACCATCGTGGAGACG-3′: (SEQ ID NO: 72); the XmaI site is underlined), or gp64(101)-f (5′-GACTCCCCGGGATTTGCTTATGTGGAGCATCAGG-3′: (SEQ ID NO: 73); the XmaI site is underlined), or gp64(154)-f (5′-GACTCCCCGGGCGCACCACACGTGCAACAAATCG-3′: (SEQ ID NO: 74); the XmaI site is underlined), or gp64(201)-f (5′-GACTCCCCGGGACACTGTGCTTCATCGAGACGGC-3′: (SEQ ID NO: 75); the XmaI site is underlined), and GP64-r DraIII (5′-GGGCACTTAGTGATATTGTCTATTACGGTTTCTAATC-3′ (SEQ ID NO: 26); the Dralll site is underlined). The obtained DNA fragments were cleaved with XmaI and DraIII, and inserted into pCAP-HA1/Vietnam digested with XmaI and DraIII. The constructed plasmids were designated pCAP-HA1/Vietnam/51, pCAP-HA1/Vietnam/101, pCAP-HA1/Vietnam/154, and pCAP-HA1/Vietnam/201.
The GenBank accession number of the amino acid sequence of the hemagglutinin of influenza virus A/H5N1/Vietnam/1203/2004 is AAW80717.
(10) Construction of Transfer Vector Plasmids pCAP-AH/345, pCAP-AH/345/467, pCAP-AH/410, pCAP-AH/410/467, pCAP-AH/473, pCAP-AH/473/467, pCAP-AH/520, pCAP-AH/520/467 of the Present Invention
An artificial gene sequence (SEQ ID NO: 76) was prepared from the amino acid sequence of the HA region of the hemagglutinin of influenza virus A/H5N1/Anhui/1/05 by codon optimization using Gene Designer available from DNA2.0, Inc. Using this artificial sequence as a template, PCR was performed using AH17-F (5′-GACTCTGCAGGATCAGATCTGTATTGGGTACC-3′: (SEQ ID NO: 77); the PstI site is underlined, and AH345-R (5′-CGATCCCGGGCTCTCTTTCTCCTCCGCTCGC-3′: (SEQ ID NO: 78); the XmaI site is underlined), or AH410-R (5′-CGATCCCGGGCGGCCTCGAACTGGGTGTTCATT-3′: (SEQ ID NO: 79); the XmaI site is underlined), or AH473-R (5′-CGATCCCGGGCGTCTCTGAGTTGAAGGCGCAC-3′: (SEQ ID NO: 80); the XmaI site is underlined, or AH520-R (5′-CGATCCCGGGCACCACTAATTTCCTCTCGCTTC-3′: (SEQ ID NO: 81); the XmaI site is underlined). The obtained DNA fragment was cleaved with PstI and XmaI, and inserted into pCAP-HA1/Anhui or pCAP-HA1/Anhui/467 digested with PstI and XmaI. The constructed plasmids were designated pCAP-AH/345, pCAP-AH/345/467, pCAP-AH/410, pCAP-AH/410/467, pCAP-AH/473, pCAP-AH/473/467, pCAP-AH/520, and pCAP-AH/520/467.
(11) Construction of Transfer Vector Plasmids pCAP-VN/346, pCAP-VN/346/467, pCAP-VN/410, pCAP-VN/410/467, pCAP-VN/473, pCAP-VN/473/467, pCAP-VN/520, and pCAP-VN/520/467 of the Present Invention
An artificial gene sequence (SEQ ID NO: 82) was prepared from the amino acid sequence of the HA region of the hemagglutinin of influenza virus A/H5N1/Vietnam/1203/2004 by codon optimization using Gene Designer available from DNA2.0, Inc. Using this artificial sequence as a template, PCR was performed using primer VN17-F (5′-GACTCTGCAGGATCAGATCTGTATCGGATATC-3′: (SEQ ID NO: 83); the PstI site is underlined), and VN346-R (5′-CGATCCCGGGCCCGCTTTTTCCTCCTCCGTTCG-3′: (SEQ ID NO: 84); the XmaI site is underlined), or VN410-R (5′-CGATCCCGGGCCTCAAACTGCGTATTCATTTTG-3′: (SEQ ID NO: 85); the XmaI site is underlined), or VN473-R (5′-CGATCCCGGGCTCTAAGCTGGAGCCTGACTTTGTC-3′: (SEQ ID NO: 86); the XmaI site is underlined), or VN520-R (5′-CGATCCCGGGCACTAATCTCCTCTCTTTTAAGTC-3′: (SEQ ID NO: 87); the XmaI site is underlined). The obtained DNA fragment was cleaved with PstI and XmaI, and inserted into pCAP-HA1/Anhui or pCAP-HA1/Anhui/467 digested with PstI and XmaI. The constructed plasmids were designated pCAP-VN/346, pCAP-VN/346/467, pCAP-VN/410, pCAP-VN/410/467, pCAP-VN/473, pCAP-VN/473/467, pCAP-VN/520, and pCAP-VN/520/467.
(12) Construction of Transfer Vector Plasmids pCAP-CO/full, pCAP-CO/full/467, pCAP-CO/19, pCAP-CO/19/467, pCAP-CO/76, pCAP-CO/76/467, pCAP-CO/205, and pCAP-CO/205/467 of the Present Invention
An artificial gene sequence (SEQ ID NO: 88) was prepared from the amino acid sequence of the CSP of Plasmodium falciparum 3D7 strain by codon optimization using Gene Designer available from DNA2.0, Inc. Using this artificial sequence as a template, PCR was performed using a pair of primers consisting of PfCSP_opt-f (5′-GACTCTGCAGATGATGCGAAAATTGGCCATACTG-3′: (SEQ ID NO: 89); the PstI site is underlined) and PfCSP_opt-r (397) (5′-CGATCCCGGGCATTGAGGAACAGAAAGGAAAGAACCATG-3′: (SEQ ID NO: 90); the XmaI site is underlined); PfCSP_opt-f (19) (5′-GACTCTGCAGCTGTTTCAGGAATACCAGTGCTATGG-3′: (SEQ ID NO: 91); (the PstI site is underlined) and PfCSP_opt-r (373) (5′-CGATCCCGGGCCTTCTCCATCTTACAAATTTTCTTTTCAATATCATTAGC-3′: (SEQ ID NO: 92); the XmaI site is underlined); PfCSP_opt-f (76) (5′-GACTCTGCAGGACGACGGAAATAATGAGGACAACG-3′: (SEQ ID NO: 93); the PstI site is underlined) and PfCSP_opt-r (373) (5′-CGATCCCGGGCCTTCTCCATCTTACAAATTTTCTTTTCAATATCATTAGC-3′: (SEQ ID NO: 92); the XmaI site is underlined); and PfCSP_opt-f (205) (5′-GACTCTGCAGAATGCAAACCCAAATGCCAATCCAAACGC-3′: (SEQ ID NO: 94); the PstI site is underlined) and PfCSP_opt-r (373) (5′-CGATCCCGGGCCTTCTCCATCTTACAAATTTTCTTTTCAATATCATTAGC-3′: (SEQ ID NO: 92); the XmaI site is underlined). The obtained DNA fragments were cleaved with PstI and XmaI, and inserted into pCAP-HA1/Anhui or pCAP-HA1/Anhui/467 digested with PstI and XmaI. The constructed plasmids were designated pCAP-CO/full, pCAP-CO/full/467, pCAP-CO/19, pCAP-CO/19/467, pCAP-CO/76, pCAP-CO/76/467, pCAP-CO/205, and pCAP-CO/205/467.
(13) Construction of Transfer Vector Plasmids pCA64-HA1/Anhui and pCA64-PfCSP (A361E) of the Present Invention
Using the Triple Cut DNA of BacVector-2000 DNA (from Novagen), PCR was performed using gp64-p-f (5′-GACTCGGACCGGCCAGATAAAAATAATCTTATCAATTAAG-3′: (SEQ ID NO: 95); the RsrII site is underlined) and gp64-p-r (5′-CGATACTAGTAGCACTGAGGCTTCTTATATACCCG-3′: (SEQ ID NO: 96); the SpeI site is underlined). The obtained DNA fragment was cleaved with RsrII and SpeI, and inserted into pCAP-HA1/Anhui or pCAP-PfCSP (A361E) digested with RsrII and SpeI to construct transfer vector plasmids pCA64-HA1/Anhui and pCA64-PfCSP (A361E) enabling the expression of a fusion protein of HA1 antigen or PfCSP antigen and gp64 protein in mammalian and insect cells under the control of the desired dual promoter consisting of CAG promoter and gp64 promoter.
(14) Construction of Transfer Vector Plasmids pCA39-HA1/Anhui and pCA39-PfCSP (A361E) of the Present Invention
Using the Triple Cut DNA of BacVector-2000 DNA (from Novagen), PCR was performed using vp39-p-f (5′-GACTCGGACCGCGTCGTACAAATCGAAATATTGTTGTG-3′: (SEQ ID NO: 97); the RsrII site is underlined) and vp39-p-r (5′-CGATACTAGTGTGATTGAGAAAGAAATCTCTTATTC-3′: (SEQ ID NO: 98); the SpeI site is underlined). The obtained DNA fragment was cleaved with RsrII and SpeI, and inserted into pCAP-HA1/Anhui or pCAP-PfCSP (A361E) digested with RsrII and SpeI to construct transfer vector plasmids pCA39-HA1/Anhui and pCA39-PfCSP (A361E) enabling the expression of a fusion protein of HA1 antigen or PfCSP antigen and gp64 protein in mammalian and insect cells under the control of the desired dual promoter consisting of CAG promoter and vp39 promoter.
(15) pCAP-CO/full/VSV, pCAP-CO/19/VSV, pCAP-CO/76/VSV, and pCAP-00/205/VSV of the Present Invention
Using pVSV-G (from Clonetech) as a template, PCR was performed using VSV-G-f (5′-GACTCCCCGGGCGTTCGAACATCCTCACATTCAAG-3′ (SEQ ID NO: 99); the XmaI site is underlined), VSV-G-r (5′-GACTCACTTAGTGCTTTCCAAGTCGGTTCATCTC-3′: (SEQ ID NO: 100); the DraIII site is underlined). The obtained DNA fragment was inserted into pCAP-CO/full, pCAP-CO/19, pCAP-CO/76, and pCAP-CO/205, each digested with XmaI and DraIII. The constructed plasmids were designated pCAP-CO/full/VSV, pCAP-CO/19/VSV, pCAP-CO/76/VSV, and pCAP-CO/205/VSV.
(1) The recombinant baculovirus was made using the kit (BacVector-2000 Transfection Kit supplied from Novagen) for making the recombinant baculovirus, by co-transfecting BacVector-2000 DNA with each of the transfer vectors: pDual-Hsp65-gp64, pDual-PbCSP-gp64, pDual-H1N1/HA1-gp64, pDual-PbTRAMP-gp64, pDual-PbAMA1D123-gp64, pDual-PbMSP-119-gp64, pDual-PfCSP-gp64, pDual-PfAMA1-gp64, pDual-Pfs25-gp64, pCP-H1N1/HA1-gp64, pCAP-H1N1/HA1-gp64, pCU-H1N1/HA1-gp64, pDual-H1N1/NP-gp64, pDual-H1N1/M2-gp64, pDual-H1N1/NAe-gp64, pDual-M2e-gp64, pCP-HA1/NC99-gp64, pCP-H1N1/HA0-gp64, pCP-H1N1/HA2-gp64, pCP-H1N1/HA1-vp39, pCP-H1N1/NP-vp39 constructed in the above Example 1, and the plasmids, pBACgus-CMV-PbCSP and pBACgus-CMV-HA-full obtained in Reference Example 1 into Sf-9 cells.
The recombinant baculoviruses made were designated as AcNPV-Dual-Hsp65, AcNPV-Dual-PbCSP, AcNPV-Dual-H1N1/HA1, AcNPV-Dual-PbTRAMP, AcNPV-Dual-PbAMA1D123, AcNPV-Dual-PbMSP-119, AcNPV-CMV-PbCSP, AcNPV-CMV-HA-full, AcNPV-H1N1/HA1, AcNPV-CAP-H1N1/HA1, AcNPV-CU-H1N1/HA1, AcNPV-Dual-H1N1/NP, AcNPV-Dual-H1N1/M2, AcNPV-Dual-H1N1/NAe, AcNPV-Dual-M2e, AcNPV-CP-HA1/NC99, AcNPV-CP-H1N1/HA0, AcNPV-CP-H1N1/HA2, AcNPV-CP-H1N1/HA1-vp39 and AcNPV-CP-H1N1/NP-vp39, respectively.
The Sf-9 cells were cultured so as to become 2×107 cells per 150 mm plate for culture (sumilon supplied from Akita Sumitomo Bakelite Co., Ltd.), and each baculovirus described above was infected at an infection multiplicity of about 5. After 5 to 6 days, the medium was centrifuged at 10,000×g at 4° C. for 25 minutes to collect a supernatant, which was further centrifuged using a Beckman ultracentrifuge (SW28 swing rotor) at 25,000 rpm at 4° C. for 90 minutes to yield viral particles.
(2) The recombinant baculovirus can be made using the kit (BacVector-2000 Transfection Kit supplied from Novagen) for making the recombinant baculovirus, by co-transfecting BacVector-2000 DNA with each of the transfer vectors: pDual-H5N1/HA1-gp64 and pDual-SARS/S-gp64 constructed in the above Example 1 into the Sf-9 cells. The recombinant baculoviruses to be made is designated as AcNPV-H5N1/HA1 and AcNPV-Dual-SARS/S, respectively.
The Sf-9 cells were cultured so as to become 2×107 cells per 150 mm plate for culture (sumilon supplied from Akita Sumitomo Bakelite Co., Ltd.), and each baculovirus described above was infected at an infection multiplicity of about 5. After 5 to 6 days, the medium can be centrifuged at 10,000×g at 4° C. for 25 minutes to collect the supernatant, which can be further centrifuged using the Beckman ultracentrifuge (SW28 swing rotor) at 25,000 rpm at 4° C. for 90 minutes to yield viral particles.
(1) Recombinant baculoviruses were produced using a kit for producing recombinant baculoviruses (BacVector-2000 Transfection Kit from Novagen) by co-transfecting BacVector-2000 DNA with each of the following transfer vectors constructed in Example 1: pCAP-PfCSP, pCAP-PfCSP/272, pCAP-PfCSP/467, pCAP-PfCSP(A361E), pCAP-PfCSP(A361E)/272, pCAP-PfCSP(A361E)/467, pCAP-PfCSP-76, pCAP-PfCSP-76/467, pCAP-PfCSP+209, pCAP-PfCSP+209/467, pCAP-PfCSP+76/209, pCAP-PfCSP+76/209/467, pCAP-HA1/Anhui, pCAP-HA1/Anhui/272, pCAP-HA1/Anhui/467, pCAP-HA1/Vietnam, pCAP-HA1/Vietnam/51, pCAP-HA1/Vietnam/101, pCAP-HA1/Vietnam/154, pCAP-HA1/Vietnam/201, pCAP-HA1/Vietnam/272, pCAP-HA1/Vietnam/467, pCAP-AH/345, pCAP-AH/345/467, pCAP-AH/410, pCAP-AH/410/467, pCAP-AH/473, pCAP-AH/473/467, pCAP-AH/520, pCAP-AH/520/467, pCAP-VN/346, pCAP-VN/346/467, pCAP-VN/410, pCAP-VN/410/467, pCAP-VN/473, pCAP-VN/473/467, pCAP-VN/520, pCAP-VN/520/467, pCAP-CO/full, pCAP-CO/full/467, pCAP-CO/19, pCAP-CO/19/467, pCAP-CO/76, pCAP-CO/76/467, pCAP-CO/205, pCAP-CO/205/467, pCA39-HA1/Anhui, pCA64-HA1/Anhui, pCA39-PfCSP(A361E), pCA64-PfCSP(A361E), pCAP-CO/full/VSV, pCAP-CO/19/VSV, pCAP-CO/76/VSV, pCAP-CO/205/VSV, pDual-Pfs25-PfCSP-gp64, pDual-PfMSP1-PfCSP-gp64 into Sf9 cells. The resulting recombinant baculoviruses were designated AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-PfCSP(A361E), AcNPV-CAP-PfCSP(A361E)/272, AcNPV-CAP-PfCSP(A361E)/467, AcNPV-CAP-PfCSP-76, AcNPV-CAP-PfCSP-76/467, AcNPV-CAP-PfCSP+209, AcNPV-CAP-PfCSP+209/467, AcNPV-CAP-PfCSP+76/209, AcNPV-CAP-PfCSP+76/209/467, AcNPV-CAP-HA1/Anhui, AcNPV-CAP-HA1/Anhui/272, AcNPV-CAP-HA1/Anhui/467, AcNPV-CAP-HA1/Vietnam, AcNPV-CAP-HA1/Vietnam/51, AcNPV-CAP-HA1/Vietnam/101, AcNPV-CAP-HA1/Vietnam/154, AcNPV-CAP-HA1/Vietnam/201, AcNPV-CAP-HA1/Vietnam/272, AcNPV-CAP-HA1/Vietnam/467, AcNPV-CAP-AH/345, AcNPV-CAP-AH/345/467, AcNPV-CAP-AH/410, AcNPV-CAP-AH/410/467, AcNPV-CAP-AH/473, AcNPV-CAP-AH/473/467, AcNPV-CAP-AH/520, AcNPV-CAP-AH/520/467, AcNPV-CAP-VN/346, AcNPV-CAP-VN/346/467, AcNPV-CAP-VN/410, AcNPV-CAP-VN/410/467, AcNPV-CAP-VN/473, AcNPV-CAP-VN/473/467, AcNPV-CAP-VN/520, AcNPV-CAP-VN/520/467, AcNPV-CAP-CO/full, AcNPV-CAP-CO/full/467, AcNPV-CAP-CO/19, AcNPV-CAP-CO/19/467, AcNPV-CAP-CO/76, AcNPV-CAP-CO/76/467, AcNPV-CAP-CO/205, AcNPV-CAP-CO/205/467, AcNPV-CA39-HA1/Anhui, AcNPV-CA64-HA1/Anhui, AcNPV-CA39-PfCSP(A361E), AcNPV-CA64-PfCSP(A361E), AcNPV-CAP-CO/full/VSV, AcNPV-CAP-CO/19/VSV, AcNPV-CAP-CO/76/VSV, AcNPV-CAP-00/205/VSV, AcNPV-Dual-Pfs25-PfCSP-64, and AcNPV-Dual-PfMSP1-PfCSP-gp64.
A recombinant virus solution for vaccine was inoculated to BALB/c female mice three times at three week intervals. In the case of injection into thigh muscle, the amount was 0.2 mL/body, and the virus solution was prepared so that the virus amount was 5×106 pfu/body.
3.2 Infection of Mice with Malaria
The mice in each group were anaesthetized with a anesthesia solution for mice, 3 weeks after the third vaccine inoculation, and infected with malaria by making Anopheles stephensi SDA 500 strain infected with Plasmodium berghei ANKA 2.34 clone bite the mice.
After the infection with malaria, death cases in each group were counted, and the survival rate of the mice in each group was calculated.
3.4 For the Malaria Infection Prevention Effect of the Pharmaceutical Composition of the Present Invention as the Vaccine, the Results of the Pharmacological Effect Test are Shown in Table 1. The Survival Rate in Each Group was Shown in Right Columns in Table 1.
As shown in Table 1, all of the mice in which the erythrocytes infected with malaria in peripheral blood had been identified were died within 38 days after the infection. Among the recombinant virus in which the antigen (CSP) gene in the sporozoite phase had been inserted, in the group (group No. 4) in which the recombinant baculovirus (Example 1 (2)) containing the transfer vector: AcNPV-Dual-PbCSP) obtained in Example 2 had been inoculated intramuscularly, 100% of the infection prevention effect was observed.
In the wild type baculovirus (group No. 2), no difference from the control group (group No. 1) was observed. In the group (group No. 3) in which the recombinant baculovirus obtained in Example 2 using the mammal promoter (AcNPV-CMV-PbCSP, including the vector in Reference Example 1) had been included, the slightly higher survival rate was observed compared with the control group, suggesting the probability that the effect by the virus inoculation appeared although it was weak.
A virus solution for vaccine was inoculated twice at 2 week intervals. The vaccine virus was injected at 106.5 PFU per mouse in thigh muscle using a syringe with 26G for insulin injection.
On a current day of the infection with influenza virus, a stored virus solution of the influenza virus A/PR/8/34 strain was naturally thawed at room temperature. The thawed stored virus solution was diluted to 1000 TCID50/0.05 mL for lower respiratory tract infection and 1000 TCID50/0.005 mL for upper respiratory tract infection using Dulbecco's Phosphate Buffer Saline: (D-PBS) containing 10% sterile BSA: bovine serum albumin to make the virus solution for challenge.
Two weeks after the second vaccine inoculation, the mice were anesthetized by intramuscularly administering 0.05 mL of the anesthesia solution for mice. The influenza virus solution made in 4.2 was inoculated in the nose of the mice at 0.005 mL for the upper respiratory tract infection or 0.05 mL for the lower respiratory tract infection.
Three days after the virus inoculation, 0.1 mL per mouse of the anesthesia solution for mice was intramuscularly administered to 4 mice in each group, and euthanized by bleeding from aorta abdominalis under the anesthesia. Subsequently, the mice were anatomized, and the lung was sterilely removed.
4.5 Records of Survival Rate of the Mice after the Inoculation of Influenza Virus
Until 11 days after the inoculation of influenza virus, the survival rate of the mice was confirmed and recorded once a day.
A lung homogenate was made by adding 3 mL of 0.1% BSA, 10 mM HEPES, Minimum Essential Medium (MEM, GIBCO) containing antibiotics and homogenizing using a polytron homogenizer. The lung homogenate was dispensed in cryotubes and stored in an ultralow temperature freezer.
A series of dilution of 10 times or 100.5 times was made using the MEM medium to which the above antibiotics and trypsin (SIGMA, T-4549, 2 mg/mL) had been added.
The medium for cell growth (MEM+10% FBS) was prepared by adding 50 mL of fetal bovine serum: FBS to 500 ml of MEM, and stored in a refrigerator until use.
4.8 Culture of MDCK (Madin-Darby Canine Kidney) Derived from Canine Kidney
The frozen and stored MDCK cells were rapidly thawed in warmed water, then suspended in 10 mL of the medium for cell growth, and the supernatant was removed by centrifugation (1000 rpm, 5 minutes, 4° C.). A cell pellet collected by centrifugation was suspended in the medium for cell growth. The cells were seeded in a culture flask, and cultured in an incubator with 5% CO2 at 37° C. After the start of the culture, morphology and growth of the cells were observed under a microscope, just before the MDCK cells became confluent, the cells were washed with D-PBS (−), the treatment with trypsin was given to the cells to disperse, and the cells were suspended in the medium for cell growth. The cell suspension was seeded in the culture flask, and the fresh medium for cell growth was added to make cell passage.
The medium in which BSA at 0.1% had been added to 500 mL of MEM (10 mM HEPES buffer was added) was rendered the medium for virus growth (MEM+0.1% BSA), and was stored in the refrigerator after the preparation until use. The antibiotics was added in use.
Just before the MDCK cells in the culture flask became confluent, the treatment with trypsin was given to the cells to disperse the cells, the number of the cells was counted, and a suspension of MDCK cells at 6×105 cells/mL was prepared using the maintenance medium. This was dispensed by 0.05 mL in each well of a 96-well plate, and cultured overnight in the CO2 incubator with 5% CO2 at 37° C.
On the subsequent day, it was confirmed that the cells adhered, and each lung homogenate dilution made previously was dispensed by 0.05 mL in each well for 6 wells in the 96-well plate, which was then cultured in the CO2 incubator with 5% CO2 at 37° C. for 3 days.
On the 3rd day of the culture, it was confirmed that the cells in the well are denatured, then a 30% formalin-containing crystal violet solution was dispensed by 0.05 mL in each well in the 96-well plate to fix and stain the cells, and the infectivity titer of the virus in the lung was calculated by Reed-Munch method.
The infectivity titers in the murine lung homogenates in the control group (inoculated with AcNPV) and the test groups (inoculated with the recombinant baculovirus [including the transfer vector: AcNPV-Dual-H1N1/HA1 obtained in Example 1(3)] and the recombinant baculovirus [containing the vector: AcNPV-CMV-H1N1/HA full obtained in Reference Example 1]) were compared. Each viral infectivity titer was converted into logarithm. The therapeutic effect among the groups was analyzed by Tukey test (Release 8.1, SAS Institute Japan Ltd) considering its multiplicity.
The results are shown in
Effect of Each Vaccine on Survival Period after the Infection with Influenza Virus
The survival periods in the control group (inoculated with AcNPV) and the vaccine groups (inoculated with AcNPV-Dual-H1N1/HA1 or AcNPV-CMV-H1N1/HA full) were compared using log rank test, and the results are shown in
Statistical analysis was performed using SAS system (SAS Institute Japan, R.8.1). A significant level was 5%.
In the group in which AcNPV-Dual-H1N1/HA1 had been inoculated intramuscularly, the infectivity titer of the virus in lung on the day 6 after the infection was significantly inhibited (p=0.0009) compared with the control group (inoculated with AcNPV). Meanwhile, in the group in which AcNPV-Dual-H1N1/HA1 had been inoculated intramuscularly, the infectivity titer of the virus in lung on the day 6 after the infection was significantly inhibited (p=0.0094) compared with the group in which AcNPV-CMV-H1N1/HA full had been inoculated.
In the group in which AcNPV-Dual-H1N1/HA1 had been inoculated intramuscularly, the survival period was significantly prolonged (p=0.0031) compared with the control group (inoculated with AcNPV). Meanwhile, the survival period in the group in which AcNPV-CMV-H1N1/HA full had been inoculated was not significantly different (p=0.7851) from that in the control group (inoculated with AcNPV). The survival period in the group in which AcNPV-Dual-H1N1/HA1 had been inoculated intramuscularly was significantly prolonged (p=0.0031) compared with the group in which AcNPV-CMV-H1N1/HA full had been inoculated.
In this evaluation system, the mouse causes influenza virus pneumonia and dies. Thus, it can be speculated that growth of the virus in lung was inhibited to reduce the death of mouse from the pneumonia by inoculating AcNPV-Dual-H1N1/HA1 intramuscularly.
The Sf-9 cells were cultured at 3×106 cells per well in a 12-well plate, and baculovirus particles of AcNPV-Dual-PbCSP, AcNPV-Dual-HSP65 or AcNPV-Dual-H1N1/HA1 obtained in Example 2 or the wild type baculovirus, AcNPV-WT as the control were infected at infection multiplicity of about 5. After 3 to 4 days, the culture supernatant was removed, the plate was rinsed three times with PBS, and then 0.2 mL per well of Leamuli solution (Tris-hydrochloride pH 6.8, 2% SDS, 10% glycerol, 0.1% bromophenol blue) containing 2% 2-mercaptoethanol was added to completely lyse the cells. The sample was boiled at 95° C. for 5 minutes, and electrophoresed on SDS-PAGE. After the electrophoresis, the protein was transferred onto a PVDF membrane (Immobilon-P supplied from Millipore) and blocking was performed by immersing the membrane in block ace (supplied from Dai Nippon Pharmaceutical Co., Ltd.) at 4° C. for 12 hours. Western blotting was performed by the following procedure. The membrane to which the proteins from the Sf-9 cells infected with each baculovirus had been transferred was incubated with a mouse anti-FLAG monoclonal antibody (supplied from Sigma) as the primary antibody, and then incubated with a biotin-labeled goat anti-mouse IgG (H+ L) antibody as the second antibody (supplied from Vector). Further, an avidin labeled alkaline phosphatase (supplied from GIBCO-BRL) was added and a color was developed with NBT/BCIP (supplied from GIBCO-BRL) to detect bands of the protein.
The results are shown in
As shown in the lanes 2, 4 and 6 in the figure, the band corresponding to the expressed fusion product of the immunogenic foreign antigen gene and the gp64 gene is observed in the recombinant baculovirus in which each antigen gene and the gp64 gene were fused and expressed under the dual promoters of the present invention.
From this, it has been identified that the immunogenic foreign antigen gene and the gp64 gene can be fused and expressed in the insect cells.
HepG2 cells were infected with AcNPV-Dual-Hsp65, or AcNPV-WT as the control at an infection multiplicity of about 1. After 24 hours, the culture supernatant was removed, the plate was rinsed three times with PBS, and then an acetone ethanol solution (7:3) cooled at −20° C. was added to fix the cells at −20° C. for 5 minutes. The blocking was performed at room temperature by adding 5% normal goat serum (supplied from Sigma). Subsequently, a mouse anti-Hsp65 antibody (Yoshida et al., Vaccine 2005) as the primary antibody and then the FITC-labeled goat anti-mouse IgG (H+ L) were added and incubated. The reacted cells were detected under a fluorescence microscope.
HepG2 cells were also cultured 1×107 cells per 100 mm plate for cell culture, and infected with the baculovirus particles, AcNPV-Dual-H1N1/HA1 or AcNPV-CMV-H1N1/HA full or AcNPV-WT as the control at an infection multiplicity of about 5. After 2 hours, the culture supernatant was removed, the plate was rinsed three times with PBS, and then the cells were cultured in the medium not containing methionine and cysteine (medium in which 10% FBS dialyzed against PBS was added to Dulbecco's Modified Eagle medium (Invitrogen)) for 3 hours. An isotope-labeled methionine and cysteine solution (TRANS35S-LABEL MP Biomedicals, Inc.) was added at a final concentration 5 μCi/mL. After 12 hours, the culture supernatant was removed, the plate was rinsed three times with PBS, and then the cells were lysed with 0.5 mL of RIPA buffer (1% Sodium deoxycholate, 1% Triton X-100, 0.1% SDS, 10 mM Tris-HCl[pH 7.5]) to make a sample. The sample was added to Protein A-Sepharose CL-4B (Pharmacia) carrier to which the serum from the mouse infected with influenza virus had been absorbed in advance, and incubated on ice for 2 hours. The carrier was washed 5 times with RIPA buffer, Leamuli solution containing 2% 2-mercaptoethanol was added, the sample was boiled at 95° C. for 5 minutes, and electrophoresed on 6% SDS-PAGE. After the electrophoresis, the gel was dried, and the protein reacted with the antibody was detected by autoradiography.
The results are shown in
As is evident from (A) in the figure, it is found that the recombinant baculovirus using the transfer vector with the dual promoters of the present invention can express the objective antigen in the mammalian cells.
This suggests that when administered to the mammal including human beings, the recombinant baculovirus produced from the recombinant transfer vector of the present invention invades into the mammalian cells, the mammalian promoter is operated, and the objective foreign antigen gene and the gp64 gene are fused in the mammalian cells to induce the acquired immunity.
In the recombinant baculovirus (AcNPV-CMV-H1N1/HA full) in which the influenza virus HA antigen gene was incorporated under the CMV promoter and the recombinant baculovirus (AcNPV-Dual-H1N1/HA1) in which the influenza virus HA antigen gene was incorporated to fuse with the gp64 gene and express under the dual promoters, it is evident that the protein which specifically reacts with the serum infected with influenza virus, i.e., the protein including the HA antigen was newly synthesized in HepG2 cells.
From this, it is thought that the recombinant baculovirus of the present invention expresses the antigen protein encoded by the desired immunogenic foreign antigen gene even in the mammalian cells, and that when the recombinant virus is administered to the mammals including human beings, with the expression of the fusion antigen in human cells, the acquired immunity specific for the antigen can be induced.
To 0.005 mL of each virus concentration solution of the baculovirus particles, AcNPV-WT, AcNPV-CMV-PbCSP, AcNPV-PbCSPsurf or AcNPV-Dual-PbCSP collected by ultracentrifuge, 0.005 mL of Leamuli solution (2×) was added, which was then boiled at 95° C. for 5 minutes, and electrophoresed on 6% SDS-PAGE. After the electrophoresis, the proteins were transferred onto the PVDF membrane (Immobilon-P supplied from Millipore) and blocking was performed by immersing the membrane in block ace (supplied from Dai Nippon Pharmaceutical Co., Ltd.) at 4° C. for 12 hours. The Western blotting was performed by the following procedure. The membrane to which the viral particle proteins had been transferred was incubated with the mouse anti-FLAG monoclonal antibody (supplied from Sigma) as the primary antibody, and then incubated with the biotin-labeled goat anti-mouse IgG (H+ L) antibody as the second antibody (supplied from Vector). Further, avidin-labeled alkaline phosphatase (supplied from GIBCO-BRL) was added and the color was developed with NBT/BCIP (supplied from GIBCO-BRL) to detect bands of the protein.
The results are shown in
As shown in the lanes 3 and 4, for AcNPV-PbCSPsurf and AcNPV-Dual-PbCSP, the strong band which indicated the presence of the fusion antigen was identified in the recombinant viral particles.
This way, from Example 7, it is found that in the recombinant baculovirus produced from the recombinant transfer vector of the present invention, the expression product of the fused gp64 gene to the desired immunogenic foreign gene can be present in the recombinant viral particles.
In order to identify whether the recombinant virus sustains the antigen expression in cultured cells, HeLa cells were infected with AcNPV-CP-H1N1/HA1, AcNPV-CAP-H1N1/HA1 or AcNPV-CU-H1N1/HA1, and the antigen expression was identified. The cells were seeded in a 24-well plate at 1.0×104 cells/well, and then infected with the virus at MOI=10, 20, 100, which was adhered for one hour. Subsequently the virus was removed from a cell culture supernatant, and the cells were cultured in an incubator. The cells were collected with time, and RNA was extracted. RT-PCR was performed with the extracted RNA as the template using the primer HA1_F01 (5′-GAGCTGAGGGAGCAATTGAG-3′ (sequence: SEQ ID NO: 101) and the primer HA1_R01 (5′-GGGTGATGAATACCCCACAG-3′ (sequence: SEQ ID NO:102). The amplified DNA was analyzed on electrophoresis.
As a result, the expression was identified in all three types, confirming that the CMV promoter can be converted to another eukaryotic promoter with respect to the recombinant baculovirus of the present invention.
1. RNA from cells infected with wild type virus at MOI=10;
2. RNA from cells infected with wild type virus at MOI=20;
3. RNA from cells infected with wild type virus at MOI=100;
4. RNA from cells infected with AcNPV-CP-H1N1/HA1 at MOI=10;
5. RNA from cells infected with AcNPV-CP-H1N1/HA1 at MOI=20;
6. RNA from cells infected with AcNPV-CP-H1N1/HA1 at MOI=100;
7. RNA from cells infected with AcNPV-CU-H1N1/HA1 at MOI=10;
8. RNA from cells infected with AcNPV-CU-H1N1/HA1 at MOI=20;
9. RNA from cells infected with AcNPV-CU-H1N1/HA1 at MOI=100;
10. RNA from cells infected with AcNPV-CAP-H1N1/HA1 at MOI=10;
11. RNA from cells infected with AcNPV-CAP-H1N1/HA1 at MOI=20; and
12. RNA from cells infected with AcNPV-CAP-H1N1/HA1 at MOI=100. The sample was collected with time 0 hour, one day, 4 days and 7 days after the infection, was amplified by RT-PCR, and amplified DNA was electrophoresed.
A solution of the recombinant virus for vaccination was inoculated to BALB/c female mice three times at three week intervals. An inoculated dose was prepared at 0.2 mL/body corresponding to 1×108 pfu/body of a virus amount for intramuscular injection at a thigh muscle. The wild type virus (AcNPV-WT), AcNPV-PbCSPsurf (Yoshida et al. Virology 316: 161-70, 2003) or AcNPV-Dual-PbCSP was injected as the vaccine.
The mouse was euthanized three weeks after the last immunization, and serum and spleen were removed from the mouse. The serum was used for measuring the specific antibody titer and the spleen was used for ELISPOT assay.
The antibody titer was measured by ELISA using a plate on which a PbCSP recombinant protein forcibly expressed in Escherichia coli and purified/recovered had been immobilized. The ELISA was performed according to the standard methods. As a result, although no increase of the antibody titer was identified in groups in which no virus had been inoculated or the wild type virus had been inoculated, the increase of the specific antibody titer could be identified in the group in which AcNPV-PbCSPsurf had been inoculated and the group in which AcNPV-Dual-PbCSP had been inoculated.
In
ELISPOT assay was performed using spleen cells from immunized mice. The spleen cells from the mouse were prepared and an appropriate number of the cells were added to MultiScreen-IP (Millipore). A peptide (amino acid sequence: SYIPSAEKI SEQ ID NO: 103) known as a CD 8 epitope of PbCSP was added thereto, which was then cultured overnight. Subsequently the reaction was performed using ELISPOT Mouse IFN-γ ELISPOT Set (BD Sciences), and a color was developed using AEC substrate set (BD Sciences). The cell number which had responded specifically for the antigen was identified by measuring colored spots. As a result, no antigen specific cell could be identified in the group in which no virus, the wild type virus or AcNPV-PbCSPsurf had been inoculated, but about 350 reacted cells per 106 spleen cells were identified in the group in which AcNPV-Dual-PbCSP had been inoculated. This has demonstrated that AcNPV-Dual-PbCSP can more significantly induce the cellular immunity than AcNPV-PbCSPsurf.
In
The M2e recombinant baculovirus (AcNPV-Dual-M2e) in an amount of 3.4×108 PFU per mouse was inoculated in thigh muscle twice at two week interval. The mice were infected with influenza virus A/PR8/34 by inoculating 0.005 mL of solution containing 1000 TCID50 of the virus intranasally two weeks after the final vaccine inoculation. On 6 days after the infection, the mice were euthanized, the lung was removed, and the amount of virus in the lung was detected using MDCK cells. As a result, no influenza virus could be detected in all mice inoculated with AcNPV-Dual-M2e. At the same time, this was the same effect as in the group in which the HA1 recombinant baculovirus vaccine (AcNPV-Dual-H1N1/HA1) (1.0×107 PFU per mouse) had been inoculated in the thigh muscle.
In
HA1/NC99 recombinant baculovirus (AcNPV-Dual-HA1/NC99) at 1.0×108 PFU per mouse was inoculated in thigh muscle twice with a two week interval. Two weeks after the final inoculation, the mouse was infected with Influenza virus A/NewCaledonia/20/99 by inoculating 0.05 mL of a solution containing the virus at 1000TCID50 in a nasal cavity. Three days after the infection, the mouse was euthanized, lung was removed and the intrapulmonary virus amount was detected using MDCK cells. As a result, no influenza virus could be detected in three of four mice inoculated with AcNPV-Dual-H1N1/NC99.
In
SEQ ID NOS: 101 and 102 represent the primers for identifying the expression of AcNPV-CP-H1N1/HA1, AcNPV-CAP-H1N1/HA1 and AcNPV-CU-H1N1/HA1.
SEQ ID NO: 103 represent a peptide known as a CD8 epitope of PbCSP.
HA1 recombinant baculovirus (AcNPV-Dual-H1N1/HA1) at 2.0×107 PFU per mouse was inoculated twice with a two week interval by inoculating 0.005 mL of the virus solution in both noses (nasal drop), inoculating 0.05 mL of the virus solution from the nose (rhinovaccination), inoculating 0.05 mL of the virus solution from a respiratory tract (through the respiratory tract) and inoculating 0.05 mL of the virus solution in thigh muscle (muscular injection). Two weeks after the final inoculation, a nasal wash, an alveolar wash and serum were collected, and the expression of the antibody specific for the influenza virus was identified. The antibody titer was measured by ELISA using a plate to which an extract of MDCK cells infected with influenza virus A/PR/8/341 had been immobilized. The ELISA was performed in accordance with standard methods. As a result, the specific IgG antibody was identified in blood from the rhinovaccination group, the intratracheal vaccination group and the intramuscular vaccination group. In particular, the antibody was identified to be strongly induced in the intratracheal vaccination group. Likewise, the antigen specific IgG antibody was also identified in the nasal wash and the alveolar wash, and in particular, the antibody was strongly induced in the intratracheal vaccination group. Furthermore, in the intratracheal vaccination group, the production of antigen specific IgA antibody was also identified in the alveolar wash.
In
In
HA1 recombinant baculovirus (AcNPV-Dual-H1N1/HA1) at 1.0×107 PFU per mouse was inoculated twice with a two week interval by the administration route of nasal drop, rhinovaccination, through the respiratory tract or muscular injection. Two weeks after the final inoculation, the mouse was infected with influenza virus A/PR/8/34 by inoculating 0.005 mL of a solution containing the virus at 1000TCID50 in the nasal cavity. Three days after the infection, the nasal wash was collected, 6 days after the infection, the lung was removed, and the intrapulmonary virus amount was detected using MDCK cells. As a result, the virus amount in the nasal cavity 3 days after the infection was remarkably reduced in the rhinovaccination group and the intratracheal vaccination group. Furthermore, in the intratracheal vaccination group, the intrapulmonary virus amount 6 days after the infection was reduced to a detection limit or lower as well as in the intramuscular vaccination group.
In
In
Sf9 cells were cultured at a concentration of 1×105 cells per well in a 48-well plate (from Corning), and infected with baculoviruses AcNPV-CAP-PfCSP, AcNPV-CAP-HA1/Anhui, and AcNPV-CAP-HA1/Vietnam obtained in Example 2, or a wild-type baculovirus AcNPV-WT as a control at an infection multiplicity of about 0.1. After 5 days, the culture supernatant was removed from each well, and then Sample Buffer Solution (+2ME, ×2) (from Wako) was added in an amount of 0.05 mL per well to completely lyse the cells. The cell lysate was heated at 100° C. for 5 minutes, and electrophoresed on 7.5% SDS-PAGE. After electrophoresis, the protein was transferred to a PVDF membrane (Immobilon-P from Millipore), and blocking was performed at 4° C. overnight by immersing the membrane in 2.5% Skim Milk/SuperBlock (from Pierce). The membrane to which the protein of Sf9 cells infected with each baculovirus had been transferred was incubated with an anti-gp64 antibody (AcV5 from eBioScience) as the primary antibody, and then incubated with a HRP-labeled goat anti-mouse IgG (H+ L) antibody (from BioRad) as the second antibody. Color was developed with an ECLplus Western Blotting Detection kit (from GE Healthcare) to detect the protein band.
As shown in Lanes 2, 3 and 4 of
The above results confirmed that when using the recombinant virus of the present invention, an immunogenic foreign antigen gene and gp64 gene can be fused and expressed as an expressed fusion product in insect cells.
Sf9 cells were cultured to a concentration of 1×107 cells per 150 mm cell culture plate (from Sumilon), and infected with each of the above-mentioned baculoviruses at an infection multiplicity of about 0.1. After 7 days, the medium was centrifuged at 3,000×g at 4° C. for 15 minutes twice, and the virus solution was layered over a 25% sucrose solution, and centrifuged using an ultracentrifuge at 25,000 rpm at 4° C. for 90 minutes to yield viral particles. 0.05 mL of Sample Buffer Solution (+2ME, ×2) (from Wako) was added to 0.05 mL each of the virus concentrates (1×108 PFU/mL) of AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, AcNPV-CAP-PfCSP/467, AcNPV-CAP-HA1/Vietnam, and AcNPV-WT collected by ultracentrifugation. The resulting mixtures were heated at 100° C. for 5 minutes, and electrophoresed on 7.5% SDS-PAGE. After the electrophoresis, the obtained proteins were transferred to PVDF membranes (Immobilon-P from Millipore), and immersed in 2.5% Skim Milk/SuperBlock (from Pierce) to perform blocking at 4° C. overnight. The membranes to which the virus solutions of AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/272, and AcNPV-CAP-PfCSP/467 had been transferred were incubated with an anti-PfCSP antibody (2A10, MR-4) as the primary antibody, and then incubated with a HRP-labeled goat anti-mouse IgG (H+ L) antibody (from BioRad) as the second antibody. The membrane to which the virus solution of AcNPV-CAP-HA1/Vietnam had been transferred was incubated with an anti-H5N1 antibody (IT-003-005 from Immune Technology) as the primary antibody, and then incubated with a HRP-labeled goat anti-rabbit IgG antibody (from GE Healthcare) as the second antibody. Color was developed with an ECLplus Western Blotting Detection kit (from GE Healthcare) to detect the bands of the proteins.
The above results of Example 4 show that a foreign gene having the desired immunogenicity and gp64 gene can be fused and expressed in recombinant viral particles of the recombinant baculovirus of the present invention produced by using the recombinant transfer vector of the present invention.
HepG2 cells were infected with AcNPV-Dual-PfMSP1-PfCSP at an infection multiplicity of 1. After 48 hours, the culture supernatant was removed, and the plate was rinsed with PBS three times. An acetone/ethanol solution (a mixed ratio of 7:3) cooled to −20° C. was added to immobilize the cells at −20° C. for 5 minutes. A 5% normal goat serum (from Sigma) was added to perform blocking at room temperature for 1 hour. To detect the expression of PfCSP, an anti-PfCSP antibody (2A10, MR-4) labeled with Alexa Flour 594 was added; and to detect the expression of PfMSP-119, an anti-PfMSP-119 antibody (5.2, MR-4) and then an anti-mouse antibody labeled with FITC were added. After incubation, the reacted cells were detected under a fluorescence microscope.
This suggests that when the recombinant baculovirus produced using the recombinant transfer vector of the present invention is administered to humans and other mammals, the virus particles enter the mammalian cells, and a mammalian promoter operates to produce a fusion product of the desired foreign antigen gene and gp64 gene in the mammalian cells, thus inducing the acquired immunity.
Virus solutions of AcNPV-WT, AcNPV-CAP-PfCSP, AcNPV-CAP-PfCSP/467, AcNPV-CAP-HA1/Anhui, and AcNPV-CAP-HA1/Vietnam concentrated by ultracentrifugation were inoculated into the thigh muscles of BALB/c female mice in an amount of 1×108 PUF twice at two week-intervals.
The mice were euthanized two weeks after the final immunization, and sera were collected from the mice and used for measuring antigen-specific antibody titers. Induction of PfCSP antigen-specific antibody titers by AcNPV-CAP-PfCSP and AcNPV-CAP-PfCSP/467 was measured by ELISA using a plate on which (NANP)4NVDPC peptide (from Sigma), i.e., B-cell epitope of PfCSP, had been immobilized. Induction of H5N1/HA antigen-specific antibody titers by AcNPV-CAP-HA1/Anhui and AcNPV-CAP-HA1/Vietnam was measured by ELISA using a plate on which purified HA antigen of H5N1 virus (IT-003-005p from Immune Technology) had been immobilized. The absorbance at OD450 nm was measured using MaxiSorp (from NUNC) as the ELISA plate, HRP-labeled goat anti-mouse IgG (H&L) antibody (from American Qualex) as the secondary antibody, and TMB (from Calbiochem) for the color reaction.
A hemagglutination inhibition (HI) test was performed using a mouse serum inoculated with AcNPV-CAP-HA1/Anhui. More specifically, the test was performed according to the method described in the instructions packaged with an influenza HI reagent “Seiken” (from Denka Seiken Co., Ltd.), using purified HA antigen of H5N1 virus (IT-003-0053p from Immune Technology). Absorption of non-specific agglutinins was performed using erythrocyte, and removal of non-specific agglutination inhibitors was performed using RDE (II) of “Seiken” (from Denka Seiken Co., Ltd.). The HI test was performed in the following manner. 0.025 mL of 10-fold diluted antiserum in a 96-well plate was subjected to 2-fold serial dilution using a diluent. To each well of the 96-well plate containing the diluted antiserum, 0.025 mL of HA antigen of H5N1 virus diluted to obtain an HA titer of 4 per 0.025 mL thereof was added. The plate was allowed to stand at room temperature for 30 minutes. 0.05 mL of an erythrocyte suspension for the reaction was added and stirred well. The mixture was allowed to stand at room temperature for 60 minutes. The final dilution of the test sample at which hemagglutination was completely inhibited was defined as the HI antibody titer.
The results show that the sera inoculated with PBS and AcNPV-WT had HI antibody titers of 10 or less, whereas the serum inoculated with AcNPV-CAP-HA1/Anhui had an HI antibody titer of 40.
The results seem to indicate that when administered to humans and other mammals, the recombinant baculovirus produced from the recombinant transfer vector of the present invention can induce an antibody effective to the desired foreign antigen gene, thus providing vaccine effects.
SEQ ID NOS: 1 and 2 are the sequences of primers PbCSP-F and PbCSP-R1 for PCR of genomic DNA from P. berghei ANKA strain;
SEQ ID NOS: 3 and 4 are the sequences of primers phsp65-F1 and phsp65-R1 for PCR of genomic DNA from M. tuberculosis H37Rv;
SEQ ID NOS: 5 and 6 are the sequences of primers phsp65-F2 and phsp65-R2 for PCR with pcDNA as a template;
SEQ ID NOS: 7 and 8 are the sequences of primers pPolh-F2 and pgp64-R2 for PCR with pBACgus-1 (supplied from Novagen) as the template for obtaining a gp64 gene DNA fragment;
SEQ ID NOS: 9 and 10 are the sequences of primers HA-f and HA-r for PCR for producing an influenza virus HA gene fragment; and
SEQ ID NOS: 11 and 12 are the sequences of primers pHA-F1 and pHA-R1 for PCR with pCR-Blunt-HA as the template.
SEQ ID NOS: 13 and 14 are the sequences of primers pTRAMP-F1 and pTRAMP-R1 for PCR of PbTRAMP gene.
SEQ ID NOS: 15 and 16 are the sequences of primers pAMA-F1 and pAMA-R1 for PCR of PbAMA1 gene domain 123 (D123).
SEQ ID NOS: 17 and 18 are the sequences of primers pMsp-F1 and pMsp-R1 for PCR of PbMSP119 gene.
SEQ ID NOS: 19 and 20 are the sequences of primers pPfCSP-F1 and pPfCSP-R1 for PCR of PfCSP gene.
SEQ ID NOS: 21 and 22 are the sequences of primers pPfAMA1-F1 and pPfAMA1-R1 for PCR of PfCSP gene from falciparum malaria parasite P. falciparum 3D7 strain.
SEQ ID NOS: 23 and 24 are the sequences of primers pPfs25-F1 and pPfs25-R1 for PCR of PfCSP gene from falciparum malaria parasite falciparum 3D7.
SEQ ID NOS: 25 and 26 are the sequences of primers Polh-f RsrII and GP64-r DraIII for PCR with pCR-Blunt-HA as the template.
SEQ ID NOS: 27 and 28 are the sequences of primers CMVenh-f FseI and CMVenh-r KpnI for PCR of CMV enhancer region.
SEQ ID NOS: 29 and 30 are the sequences of primers UBBp-f KpnI and UBBp-r RsrII for PCR of UBB promoter region.
SEQ ID NOS: 31 and 32 are the sequences of primers NP-f EcoRI and NP-r Cfr9I for RT-PCR of genomic RNA from influenza virus PR8/34 strain;
SEQ ID NOS: 33 and 34 are the sequences of primers M2-f EcoRI and M2-r Cfr9I for RT-PCR of genomic RNA from influenza virus PR8/34 strain;
SEQ ID NOS: 35 and 36 are the sequences of primers NAe-f EcoRI and NAe-r Cfr9I for RT-PCR of genomic RNA from influenza virus PR8/34 strain;
SEQ ID NOS: 37 and 38 are the sequences of primers M2-f EcoRI and M2e-r Cfr9I for PCR with pDual-H1N1/M2-gp64 as a template;
SEQ ID NOS: 39 and 40 are the sequences of primers HA1-f EcoRI and HA1-r CFr9I (NC99) for RT-PCR of genomic RNA from NewCaledonia99/20(NC99);
SEQ ID NOS: 41 and 42 are the sequences of primers HA0-f EcoRI and HA2-r Cfr9I for PCR with pCR-Blunt-HA as a template;
SEQ ID NOS: 43 and 44 are the sequences of primers HA2-f EcoRI and HA2-r Cfr9I for PCR with pCR-Blunt-HA as a template;
SEQ ID NOS: 45 and 46 are the sequences of primers vp39-f and vp39-r for PCR of vp39 gene region.
SEQ ID NOS: 47 and 48 are the sequences of primers Polh-S1 and HA1-r EcoRI for PCR of HA1 gene fragment.
SEQ ID NOS: 49 and 50 are the sequences of primers NP-f 5 EcoRI and NP-r EcoRI for PCR with pDual-H1N1/NP-gp64 as a template.
SEQ ID NOS: 3 and 4 are the sequences of primers phsp65-F1 and phsp65-R1 for PCR of genomic DNA of M. tuberculosis H37Rv.
SEQ ID NOS: 5 and 6 are the sequences of primers phsp65-F2 and phsp65-R2 for PCR with pcDNA-hps65 as a template.
SEQ ID NOS: 7 and 8 are the sequences of primers pPolh-F2 and pgp64-R2 for PCR with pBACsurf-1 as a template to produce a gp64 gene DNA fragment.
SEQ ID NOS: 9 and 10 are the sequences of primers HA-f and HA-r for PCR to produce an influenza virus HA gene fragment.
SEQ ID NOS: 11 and 12 are the sequences of primers pHA-F1 and pHA-R1 for PCR with pCR-Blunt-HA as a template.
SEQ ID NOS: 25 and 26 are the sequences of primers Polh-f RsrII and GP64-r DraIII for PCR with pBACsurf-HA1 as a template.
SEQ ID NOS: 31 and 32 are the sequences of primers NP-f EcoRI and NP-r Cfr9I for RT-PCR of genomic RNA of influenza virus PR/8/34 strain.
SEQ ID NOS: 51, 52, and 26 are the sequences of primers gp64 (272)-f, gp64 (467)-f, and GP64-r DraIII for PCR of pCAP-H1N1/HA1-64.
SEQ ID NOS: 53 and 54 are the sequences of primers PfCSP-f (19) and PfCSP-r (373) for PCR with P. falciparum genomic DNA as a template.
SEQ ID NOS: 15 and 16 are the sequences of primers pAMA-F1 and pAMA1-R1 for PCR with P. berghei genomic DNA as a template.
SEQ ID NOS: 19 and 20 are the sequences of primers pPfCSP-F1 and pPfCSP-R1 for PCR with P. falciparum genomic DNA as a template.
SEQ ID NOS: 23 and 55 are the sequences of primers pPfs25-F1 and pPfs25-R2 for PCR with P. falciparum genomic DNA as a template.
SEQ ID NOS: 56 and 57 are the sequences of primers pPfMSP119-F1 and pPfMSP119-R2 for PCR with P. falciparum genomic DNA as a template.
SEQ ID NOS: 53 and 58 are the sequences of primers PfCSP-f (19) and PfCSP-r (373 A361E) for PCR with pCAP-PfCSP as a template.
SEQ ID NOS: 59 and 58 are the sequences of primers PfCSP-f (76) and PfCSP-r (373 A361E) for PCR with pCAP-PfCSP as a template.
SEQ ID NO: 60 is the sequence of an artificial gene (PfCSP+) produced from the amino acid sequence of the PfCSP of P. falciparum 3D7 strain (in which, however, the A at the 361-position was replaced by E) using codons frequently used in Sf9 and human cells.
SEQ ID NOS: 61 and 62 are the sequences of primers PfCSP-f (+209) and PfCSP-r (+A361E) for PCR with PfCSP+ as a template.
SEQ ID NOS: 63, 64, 65 and 64 are the sequences of primers PfCSP-f (+76), PfCSP-r (+128), PfCSP-f (+209) BamHI, and PfCSP-r (+A361E) for PCR with PfCSP+ as a template.
SEQ ID NO: 66 is the sequence of an artificial gene produced from the amino acid sequence of the HA1 region of the hemagglutinin of influenza virus H5N1/Anhui/1/05 using codons frequently used in Sf9 and human cells.
SEQ ID NOS: 67 and 68 are the sequences of primers AH-F1 (5′-CAGTCTGCAGGACCAGATTTGCATC-3′: (SEQ ID NO: 67); the PstI site is underlined) and AH-R4 (5′-CAGTCCCGGGCTCTCTTGCGCCTGC-3′: (SEQ ID NO: 68); the XmaI site is underlined) for PCR with the artificial gene sequence of SEQ ID NO: 66 as a template.
SEQ ID NO: 69 is the sequence of an artificial gene produced from the amino acid sequence of the HA1 region of the hemagglutinin of influenza virus H5N1/Vietnam/1203/04 using codons frequently used in Sf9 and human cells.
SEQ ID NOS: 70 and 71 are the sequences of primers VN-F1 (5′-CAGTCTGCAGGACCAGATCTGTATC-3′: (SEQ ID NO: 70); the PstI site is underlined), and VN-R4 (5′-CAGTCCCGGGCTCTCTTCTTCCTGC-3′: (SEQ ID NO: 71); the XmaI site is underlined) for PCR with the artificial gene sequence of SEQ ID NO: 69 as a template.
SEQ ID NOS: 72, 73, 74, 75, and 26 are the sequences of primers gp64(51)-f (5′-GACTCCCCGGGTGGAAATCACCATCGTGGAGACG-3′: (SEQ ID NO: 72); the XmaI site is underlined), gp64(101)-f (5′-GACTCCCCGGGATTTGCTTATGTGGAGCATCAGG-3′: (SEQ ID NO: 73); the XmaI site is underlined), gp64(154)-f (5′-GACTCCCCGGGCGCACCACACGTGCAACAAATCG-3′: (SEQ ID NO: 74); the XmaI site is underlined), gp64(201)-f (5′-GACTCCCCGGGACACTGTGCTTCATCGAGACGGC-3′: (SEQ ID NO: 75); the XmaI site is underlined), and GP64-r DraIII (5′-GGGCACTTAGTGATATTGTCTATTACGGTTTCTAATC-3′ (SEQ ID NO: 26); the Dralll site is underlined).
SEQ ID NO: 76 is the sequence of an artificial gene produced from the amino acid sequence of the HA1 region of the hemagglutinin of influenza virus H5N1/Anhui/1/05 by codon optimization using Gene Designer available from DNA2.0, Inc.
SEQ ID NOS: 77, 78, 79, 80, and 81 are the sequences of AH17-F (5′-GACTCTGCAGGATCAGATCTGTATTGGGTACC-3′: (SEQ ID NO: 77); the PstI site is underlined, and AH345-R (5′-CGATCCCGGGCTCTCTTTCTCCTCCGCTCGC-3′: (SEQ ID NO: 78); the XmaI site is underlined), AH410-R (5′-CGATCCCGGGCGGCCTCGAACTGGGTGTTCATT-3′: (SEQ ID NO: 79); the XmaI site is underlined), AH473-R (5′-CGATCCCGGGCGTCTCTGAGTTGAAGGCGCAC-3′: (SEQ ID NO: 80); the XmaI site is underlined, and AH520-R (5′-CGATCCCGGGCACCACTAATTTCCTCTCGCTTC-3′: (SEQ ID NO: 81); the XmaI site is underlined) for PCR with the artificial gene sequence of SEQ ID NO: 76 as a template.
SEQ ID NO: 82 is the sequence of an artificial gene produced from the amino acid sequence of the HA1 region of the hemagglutinin of influenza virus H5N1/Vietnam/1203/04 by codon optimization using Gene Designer available from DNA2.0, Inc.
SEQ ID NOS: 83, 84, 85, 85, and 87 are the sequences of primers VN17-F (5′-GACTCTGCAGGATCAGATCTGTATCGGATATC-3′: (SEQ ID NO: 83); the PstI site is underlined), and VN346-R (5′-CGATCCCGGGCCCGCTTTTTCCTCCTCCGTTCG-3′: (SEQ ID NO: 84); the XmaI site is underlined), VN410-R (5′-CGATCCCGGGCCTCAAACTGCGTATTCATTTTG-3′: (SEQ ID NO: 85); the XmaI site is underlined), VN473-R (5′-CGATCCCGGGCTCTAAGCTGGAGCCTGACTTTGTC-3′: (SEQ ID NO: 86); the XmaI site is underlined), and VN520-R (5′-CGATCCCGGGCACTAATCTCCTCTCTTTTAAGTC-3′: (SEQ ID NO: 87); the XmaI site is underlined) for PCR with the artificial gene sequence of SEQ ID NO: 82 as a template.
SEQ ID NO: 88 is the sequence of an artificial gene produced from the amino acid sequence of the CSP of Plasmodium falciparum 3D7 strain by codon optimization using Gene Designer available from DNA2.0, Inc.
SEQ ID NOS: 89, 90, 91, 92, and 93 are the sequences of primers PfCSP_opt-f (5′-GACTCTGCAGATGATGCGAAAATTGGCCATACTG-3′: (SEQ ID NO: 89); the PstI site is underlined), PfCSP_opt-r (397) (5′-CGATCCCGGGCATTGAGGAACAGAAAGGAAAGAACCATG-3′: (SEQ ID NO: 90); the XmaI site is underlined), PfCSP_opt-f (19) (5′-GACTCTGCAGCTGTTTCAGGAATACCAGTGCTATGG-3′: (SEQ ID NO: 91); (the PstI site is underlined), PfCSP_opt-1 (373) (5′-CGATCCCGGGCCTTCTCCATCTTACAAATTTTCTTTTCAATATCATTAGC-3′: (SEQ ID NO: 92); (the XmaI site is underlined), PfCSP_opt-f (76) (5′-GACTCTGCAGGACGACGGAAATAATGAGGACAACG-3′: (SEQ ID NO: 93); the PstI site is underlined), and PfCSP_opt-f (205) (5′-GACTCTGCAGAATGCAAACCCAAATGCCAATCCAAACGC-3′: (SEQ ID NO: 94); the PstI site is underlined) for PCR with the artificial gene sequence of SEQ ID NO: 88 as a template.
SEQ ID NOS: 95, 96, 97, and 98 are the sequences of primers gp64-p-f (5′-GACTCGGACCGGCCAGATAAAAATAATCTTATCAATTAAG-3′: (SEQ ID NO: 95); the RsrII site is underlined), gp64-p-r (5′-CGATACTAGTAGCACTGAGGCTTCTTATATACCCG-3′: (SEQ ID NO: 96); the SpeI site is underlined), and vp39-p-f (5′-GACTCGGACCGCGTCGTACAAATCGAAATATTGTTGTG-3′: (SEQ ID NO: 97); the RsrII site is underlined), and vp39-p-r (5′-CGATACTAGTGTGATTGAGAAAGAAATCTCTTATTC-3′: (SEQ ID NO: 98); the SpeI site is underlined) for PCR with Baculovirus genomic DNA as a template.
SEQ ID NOS: 99 and 100 are the sequences of primers VSV-G-f (5′-GACTCCCCGGGCGTTCGAACATCCTCACATTCAAG-3′ (SEQ ID NO: 99); the XmaI site is underlined), and VSV-G-r (5′-GACTCACTTAGTGCTTTCCAAGTCGGTTCATCTC-3′: (SEQ ID NO: 100); the DraIII site is underlined) for PCR with pVSV-G as a template.
SEQ ID NOS: 101 and 102 are the sequences of primers for detecting expression of AcNPV-CP-H1N1/HA1, AcNPV-CAP-H1N1/HA1 and AcNPV-CU-H1N1/HA1.
SEQ ID NOS: 103 is a polypeptide which is known as CD8 epitope of PbCSP.
SEQ ID NOS: 104 is the amino acid sequence of PfCSP protein. (GENBANK Accession number XP—001351122)
SEQ ID NOS: 105 is the amino acid sequence of HA/A/Anhui/1/2005 protein. (GENBANK Accession number ABD28180)
SEQ ID NOS: 106 is the amino acid sequence of HA/A/Vietnam/1203/2004 protein. (GENBANK Accession number AAW80717)
SEQ ID NOS: 107 is the amino acid sequence of PfMSP1 protein. (GENBANK Accession number XP—001352170)
SEQ ID NOS: 108 is the amino acid sequence of Pfs25 protein. (GENBANK Accession number XP—001347587)
SEQ ID NOS: 109 is the polynucleotide sequence of PfCSP gene. (GENBANK Accession number XM—001351086)
SEQ ID NOS: 110 is the polynucleotide sequence of HA/A/Anhui/1/2005 gene. (GENBANK Accession number DQ371928)
SEQ ID NOS: 111 is the polynucleotide sequence of HA/A/Vietnam/1203/2004 gene. (GENBANK Accession number AY818135)
SEQ ID NOS: 113 is the polynucleotide sequence of PfMSP1 gene. (GENBANK Accession number XM—001352134)
SEQ ID NOS: 114 is the polynucleotide sequence of Pfs25 gene. (GENBANK Accession number XM—001347551)
| Number | Date | Country | Kind |
|---|---|---|---|
| 2006-32863 | Feb 2006 | JP | national |
| 2007-205785 | Aug 2007 | JP | national |
This is a Divisional application of U.S. application Ser. No. 12/192,927 filed on Aug. 15, 2008, which is a Continuation-in-Part of U.S. application Ser. No. 12/278,916 filed on Aug. 8, 2008 (national phase entry of the International application No. PCT/JP2007/052195) claiming priority of the Japanese Application No. 2006-032863 and on the International Patent Application filed on Aug. 6, 2008 claiming priority of the Japanese Application No. 2007-205785; entire contents of which are incorporated by reference herein.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12192927 | Aug 2008 | US |
| Child | 13617825 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12278916 | Aug 2008 | US |
| Child | 12192927 | US |
