Methods for the propagation of modified influenza viruses in embryonated eggs
View Patent ↗The present invention relates, to novel methods and substrates for the propagation of viruses. The invention relates to IFN-deficient substrates and methods for propagating viruses in these unconventional substrates. In particular, the invention relates to methods of propagating viruses in immature embryonated eggs, preferably six- to nine-day-old chicken eggs. The methods of the invention are particularly attractive for growing viruses suitable for use in vaccine and pharmaceutical formulations.
1. A method for vaccine production comprising:
(a) propagating in an embryonated chick egg six to nine days old a genetically engineered, attenuated influenza virus, in which the genome of the attenuated influenza virus encodes a truncated NS1 protein of between 90 and 130 amino acid residues of the first N-terminal 90 to 130 amino acid residues of an NS1 protein of the same or a different influenza virus strain, so that the genetically engineered, attenuated influenza virus expresses the truncated NS1 protein and has an impaired interferon antagonist phenotype, wherein the N-terminal amino acid of the NS1 protein of the same or a different influenza virus strain is 1, and wherein the influenza virus is not influenza C virus; and
(b) collecting progeny virus,
wherein the virus is grown to sufficient quantities and under conditions that are free from contamination, such that the progeny virus is suitable for formulation into a vaccine.
2. The method of claim 1 , wherein the genetically engineered, attenuated influenza virus is propagated in the allantoic cavity of the embryonated egg.
3. The method of claim 1 , wherein the embryonated egg is six days old.
4. The method of claim 1 , wherein the embryonated egg is seven days old.
5. The method of claim 1 , wherein the embryonated egg is eight days old.
6. The method of claim 1 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of between 90 and 100 amino acid residues of the first N-terminal 90 to 100 amino acid residues of the NS1 protein of the same or a different influenza virus strain.
7. The method of claim 1 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of between 100 and 110 amino acid residues of the first N-terminal 100 to 110 amino acid residues of the NS1 protein of the same or a different influenza virus strain.
8. The method of claim 1 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of between 110 and 120 amino acid residues of the first N-terminal 110 to 120 amino acid residues of the NS1 protein of the same or a different influenza virus strain.
9. The method of claim 1 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of between 120 and 130 amino acid residues of the first N-terminal 120 to 130 amino acid residues of the NS1 protein of the same or a different influenza virus strain.
10. The method of claim 1 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of amino acid residues 1 to 130, amino acid residues 1 to 124, amino acid residues 1 to 120, amino acid residues 1 to 110, amino acid residues 1 to 100, amino acid residues 1 to 99, or amino acid residues 1 to 90 of the NS1 protein of the same or a different influenza virus strain, wherein 1 is the N-terminal amino acid residue of the NS1 protein of the same or a different influenza virus strain.
11. The method of claim 10 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of amino acid residues 1 to 130 of the NS1 protein of the same or a different influenza virus strain.
12. The method of claim 10 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of amino acid residues 1 to 124 of the NS1 protein of the same or a different influenza virus strain.
13. The method of claim 10 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of amino acid residues 1 to 120 of the NS1 protein of the same or a different influenza virus strain.
14. The method of claim 10 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of amino acid residues 1 to 110 of the NS1 protein of the same or a different influenza virus strain.
15. The method of claim 10 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of amino acid residues 1 to 100 of the NS1 protein of the same or a different influenza virus strain.
16. The method of claim 10 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of amino acid residues 1 to 99 of the NS1 protein of the same or a different influenza virus strain.
17. The method of claim 10 , in which the attenuated influenza virus genome encodes a truncated NS1 protein of amino acid residues 1 to 90 of the NS1 protein of the same or a different influenza virus strain.
18. The method of claim 1 , wherein the genetically engineered, attenuated influenza virus is an influenza A virus.
19. The method of claim 1 , wherein the genetically engineered, attenuated influenza virus is an influenza B virus.
20. The method of claim 1 , wherein the genetically engineered, attenuated influenza virus is engineered to encode a foreign antigen.
21. The method of claim 1 , wherein the genetically engineered, attenuated influenza virus is engineered to encode an epitope from an infectious agent other than an influenza virus.
22. The method of claim 1 , wherein the genetically engineered, attenuated influenza virus is engineered to encode an epitope from another virus.
23. The method of claim 1 , wherein the genetically engineered, attenuated influenza virus is engineered to encode an epitope from a bacteria.
24. The method of claim 1 , wherein the genetically engineered, attenuated influenza virus was propagated in a cell line prior to introduction into the embryonated egg.
25. The method of claim 24 , wherein the cell line is an interferon deficient cell line.