Recombinant influenza viruses for vaccines and gene therapy

Abstract

A method for producing influenza virus particles for preparation of a vaccine. The method comprises growing reassortant influenza viruses to produce virus particles and recovering the produced virus particles. The reassortant influenza viruses are produced in cultured cells in the absence of helper virus by introducing into the cultured cells expression vectors sufficient to produce genomic vRNA or antigenomic vRNA (cRNA) segments in the cells of reassortant influenza viruses. The method produces a nucleoprotein and an RNA dependent RNA polymerase in the cells so that RNP complexes containing the genomic vRNA segments of the reassortant influenza viruses are formed. The method uses expression vectors containing HA, NA, non-HA and non-NA vRNA segments in which the HA and NA vRNA segments are HA and NA vRNA segments of a viral strain different from a strain that contains all of the non-HA and non-NA vRNA segments.

1 . A method for producing influenza virus particles for preparation of a vaccine, comprising:
 growing reassortant influenza viruses to produce virus particles and recovering said produced virus particles, wherein said reassortant influenza viruses are produced in cultured cells in the absence of helper virus by introducing into said cultured cells expression vectors sufficient to produce in said cells the genomic vRNA or antigenomic vRNA (cRNA) segments of said reassortant influenza viruses and producing in said cells a nucleoprotein and an RNA dependent RNA polymerase so that RNP complexes containing the genomic vRNA segments of said reassortant influenza viruses are formed   wherein said expression vectors encode HA, NA, non-HA and non-NA vRNA segments and wherein the HA and NA vRNA segments are HA and NA vRNA segments of a viral strain different from a strain that contains all of the non-HA and non-NA vRNA segments.   
     
     
         2 . The method of  claim 1 , wherein one or more further expression vectors are employed in said cells to express one or more proteins selected from said nucleoprotein and subunits of a RNA-dependent RNA polymerase. 
     
     
         3 . The method of  claim 1 , wherein a cell line is employed which is capable of expressing one or more of said nucleoprotein and the subunits of RNA-dependent RNA polymerase. 
     
     
         4 . The method of  claim 1 , wherein said virus is an influenza virus of type A, B or C. 
     
     
         5 . The method of  claim 1 , wherein said cells are selected from cells which are deficient in interferon activity and capable of supporting growth of said viruses. 
     
     
         6 . The method of  claim 1 , wherein said expression vectors are capable of expressing genomic vRNA segments of said viruses. 
     
     
         7 . The method of  claim 1 , wherein said growing of reassortant influenza viruses to produce virus particles occurs in an egg. 
     
     
         8 . The method of  claim 1 , wherein all the required expression vectors are cotransfected into said cells by use of a liposomal transfection reagent. 
     
     
         9 . The method of  claim 1 , wherein each of said expression vectors is a plasmid. 
     
     
         10 . The method of  claim 2 , wherein each of said expression vectors is a plasmid. 
     
     
         11 . The method of  claim 1 , wherein each vRNA segment of said viruses or the corresponding cRNAs is present in a separate expression vector. 
     
     
         12 . The method of  claim 1 , wherein the expression of each vRNA segment or cRNA was under the control of a promoter sequence derived from a mammalian Pol I promoter. 
     
     
         13 . The method of  claim 12 , wherein said promoter sequence is a truncated human Pol I promoter sequence consisting of nucleotides −250 to −1 of the corresponding native promoter or a functional derivative thereof. 
     
     
         14 . The method of  claim 1 , wherein the coding sequence for each vRNA segment or cRNA in said expression vectors is followed by a ribozyme sequence or transcription terminator to ensure a correct 3′ end of each said RNA. 
     
     
         15 . The method of  claim 2 , wherein expression of one or more viral proteins from said further expression vectors is under the control of cytomegalovirus promoter. 
     
     
         16 . A method for producing influenza virus particles comprising producing in a cell all of the genomic RNA of an influenza virus by expressing from DNA introduced into the cell at least one or more of genomic RNA or cRNA of the influenza virus and producing in the cell RNA dependent RNA polymerase and nucleoprotein and assembling in the cell the influenza virus, said cell being free of helper virus, wherein said cell is selected from cells which are deficient in interferon activity and capable of supporting growth of said virus. 
     
     
         17 . The method of  claim 16 , wherein said virus is an influenza virus of type A, B or C. 
     
     
         18 . The method of  claim 1 , wherein said reassortant influenza viruses are at least 99% free from contaminating viruses. 
     
     
         19 . A method for producing influenza virus particles for preparation of a vaccine, comprising:
 growing a reassortant influenza virus to produce virus particles and recovering said produced virus particles, wherein said reassortant influenza virus is produced in cultured cells in the absence of helper virus by introducing into said cultured cells expression vectors to produce in said cells the genomic vRNA or antigenomic vRNA (cRNA) segments of a reassortant influenza virus and producing in said cells a nucleoprotein and an RNA dependent RNA polymerase so that RNP complexes containing the genomic vRNA segments of said reassortant influenza virus are formed,   wherein said expression vectors encode at least 4 different vRNA (or cRNA) segments and wherein each said different vRNA segment is from a single influenza virus strain, wherein all said different vRNA segments are not from the same influenza virus strain, wherein said different vRNA segments include an HA and an NA vRNA segment both of which are from the same influenza virus strain, and wherein said different vRNA segments are selected from PB2, PRI, PA, HA, NP, NA, M and NS.   
     
     
         20 . The method of  claim 19 , wherein said expression vectors encode at least 5 different vRNA segments. 
     
     
         21 . The method of  claim 19 , wherein said expression vectors encode at least 6 different vRNA segments. 
     
     
         22 . The method of  claim 19 , wherein said expression vectors encode at least 7 different vRNA segments. 
     
     
         23 . The method of  claim 19 , wherein said expression vectors encode 8 different vRNA segments. 
     
     
         24 . The method of  claim 19 , wherein all of said different vRNA segments other than HA and NA are from the same influenza virus strain.