Respiratory syncytial virus having cleavage-resistant G protein and related materials and methods
Embodiments disclosed herein provide compositions, methods, and uses for respiratory syncytial viruses (RSV) and immunogenic compositions thereof. Certain embodiments provide RSV having cleavage-resistant mutated attachment (G) glycoproteins. In some embodiments, the cleavage-resistant G protein mutants increase production of live attenuated RSV in host cells. Also provided are methods for amplifying RSV in host cells, wherein the amplified RSV has full length G protein. In certain embodiments, the amplified RSV having full length G protein is formulated into immunogenic compositions, including vaccines. Other embodiments provide methods for inducing an effective immune response against RSV infection in a subject.
1. A method for producing an immunogenic composition against respiratory syncytial virus (RSV) comprising:
providing a Vero host cell culture;
inoculating the Vero host cell culture with an RSV comprising a mutated attachment (G) protein having an amino acid substitution at one or more amino acids selected from: L208; K209; K212; K213; and D214 of the attachment protein represented by SEQ ID NO: 1, wherein the RSV is attenuated;
incubating the Vero host cell culture with the RSV;
harvesting RSV following the incubation step; and
formulating the harvested RSV into an immunogenic composition against RSV.
2. The method of claim 1 , further comprising purifying the harvested RSV.
3. The method of claim 1 , wherein the Vero host cell culture is incubated with the RSV for a time period of between about 30 minutes and about 4 hours.
4. The method of claim 1 , wherein the RSV is harvested at a time of between 48 and 96 hours following inoculation.
5. The method of claim 1 , wherein the formulating step comprises bringing the harvested attenuated RSV into association with a pharmaceutically acceptable carrier, vehicle, or excipient, an adjuvant, or a combination thereof.
6. A method for producing an immunogenic composition against respiratory syncytial virus (RSV) comprising:
providing a Vero host cell culture;
inoculating the Vero host cell culture with an RSV strain having a wild-type G protein or a mutated RSV comprising a mutated attachment (G) protein having an amino acid substitution at one or more amino acids selected from: L208; K209; K212; K213; and D214 of the attachment protein represented by SEQ ID NO: 1, wherein the RSV having the wild-type G protein or the mutated RSV of claim 1 is attenuated;
incubating the inoculated Vero host cell culture;
inhibiting Vero cell cathepsin L during the incubating step;
harvesting RSV following the incubation step; and
formulating the harvested RSV into an immunogenic composition against RSV.
7. The method of claim 6 , further comprising purifying the harvested RSV.
8. The method of claim 6 , wherein the formulating step comprises bringing the harvested attenuated RSV into association with a pharmaceutically acceptable carrier, vehicle, or excipient, an adjuvant, or a combination thereof.
9. The method of claim 6 , wherein Vero cell cathepsin L is inhibited by incubating the inoculated Vero host cell culture with at least one cathepsin L inhibitor.
10. The method of claim 9 , wherein the at least one cathepsin L inhibitor selected from the group consisting of: 3-epiursolic acid; 3-(hydroxyimino)oleanolic acid; 3-(hydroxyimino)masticadienoic acid; ALLM; ALLN; biotin-FA-FMK; CAA0225; CA-074; CA-074 Me; Calpain Inhibitor I; Calpain Inhibitor II; Calpain Inhibitor III; Calpain Inhibitor IV; Calpain Inhibitor V; Calpain Inhibitor VI; Calpeptin; Catfish muscle cathepsin inhibitor; Cathepsin inhibitor peptide; Cathepsin Inhibitor 1; Cathepsin L inhibitor; Cathepsin L inhibitor I; Cathepsin L inhibitor II; Cathepsin L inhibitor III; Cathepsin L inhibitor IV; Cathepsin L inhibitor Katunuma; CLIK148; Cathepsin/subtilisin inhibitor; Chagasin; Chloroketones; Chymostatin; Clitocypin; CTLA-2 alpha; CTLA-2 beta; Cystatins; Disulfiram; E-64; E-64-c; E-64-d; Gallinamide A; Hurpin; KD-1; KGP94; L006235; Leupeptin; L-transepoxysuccinyl-L Leu cylamine; MDL28170; Mu-Phe-hPhe-FMK; N-(1-Napthalenlsulfonyl)-Ile-Trp-aldehyde; N-Acetyl-L-Leucyl-L-Leucyl-L-methional; Napsul-Ile-Trp-CHO (NSITC); Oxocarbazate; Peptidomimetic 2-cyanopyrrolidines; Phenylmethanesulfonyl fluoride; Protein C inhibitor; SID 26681509; Squamous cell carcinoma antigen; Thiocarbazate; Triterpenoids; Z-FA-FMK; Z-FF-FMK; ZINC03846634 (APQ); ZINC08764437 (NFP); Z-Phe-Ala-CHN2; Z-Phe-Phe-CH2F; Z-Phe-Tyr (tBu)-diazomethylketone; Z-Phe-Tyr-aldehyde; a-macroglobulin; and combinations thereof.
11. The method of claim 6 , wherein cathepsin L is inhibited by silencing a gene encoding cathepsin L in cells of the host cell culture.
12. The method of claim 11 , wherein the gene encoding cathepsin L is silenced by one or more molecules selected from: siRNA; miRNA; shRNA; and combinations thereof.
13. The method of claim 6 , wherein the inoculated Vero host cell culture is incubated with the RSV for a time period of between about 30 minutes and about 4 hours.
14. The method of claim 6 , wherein the RSV is harvested at a time of between 48 and 96 hours following inoculation.
15. An immunogenic composition against RSV produced by the method of claim 1 , wherein the immunogenic composition comprises a pharmaceutically acceptable carrier, vehicle, or excipient, an adjuvant, or a combination thereof.
16. An immunogenic composition against RSV produced by the method of claim 6 , wherein the immunogenic composition comprises a pharmaceutically acceptable carrier, vehicle, or excipient, an adjuvant, or combination thereof.
17. A method for inducing an effective immune response against respiratory syncytial virus (RSV) infection in a subject, comprising administering to the subject an immunologically effective dose of the immunogenic composition against RSV of claim 1 .
18. The method of claim 17 , wherein the subject is human.
19. The method of claim 17 , wherein the subject is a human infant or child.
20. The method of claim 17 , wherein the immunogenic composition against RSV is administered via an administration route selected from: intranasal administration; subcutaneous administration; intramuscular administration; intradermal administration; and oral administration.
21. The method of claim 17 , further comprising administering at least one subsequent immunologically effective dose of the immunogenic composition against RSV.
22. The method of claim 1 , further comprising inhibiting Vero cell cathepsin L during the incubating step.
23. The method of claim 22 , wherein Vero cell cathepsin L is inhibited by incubating the Vero host cell culture with the attenuated RSV with at least one cathepsin L inhibitor.
24. The method of claim 23 , wherein the at least one cathepsin L inhibitor selected from the group consisting of: 3-epiursolic acid; 3-(hydroxyimino)oleanolic acid; 3-(hydroxyimino)masticadienoic acid; ALLM; ALLN; biotin-FA-FMK; CAA0225; CA-074; CA-074 Me; Calpain Inhibitor I; Calpain Inhibitor II; Calpain Inhibitor III; Calpain Inhibitor IV; Calpain Inhibitor V; Calpain Inhibitor VI; Calpeptin; Catfish muscle cathepsin inhibitor; Cathepsin inhibitor peptide; Cathepsin Inhibitor 1; Cathepsin L inhibitor; Cathepsin L inhibitor I; Cathepsin L inhibitor II; Cathepsin L inhibitor III; Cathepsin L inhibitor IV; Cathepsin L inhibitor Katunuma; CLIK148; Cathepsin/subtilisin inhibitor; Chagasin; Chloroketones; Chymostatin; Clitocypin; CTLA-2 alpha; CTLA-2 beta; Cystatins; Disulfiram; E-64; E-64-c; E-64-d; Gallinamide A; Hurpin; KD-1; KGP94; L006235; Leupeptin; L-transepoxysuccinyl-L Leu cylamine; MDL28170; Mu-Phe-hPhe-FMK; N-(1-Napthalenlsulfonyl)-Ile-Trp-aldehyde; N-Acetyl-L-Leucyl-L-Leucyl-L-methional; Napsul-Ile-Trp-CHO (NSITC); Oxocarbazate; Peptidomimetic 2-cyanopyrrolidines; Phenylmethanesulfonyl fluoride; Protein C inhibitor; SID 26681509; Squamous cell carcinoma antigen; Thiocarbazate; Triterpenoids; Z-FA-FMK; Z-FF-FMK; ZINC03846634 (APQ); ZINC08764437 (NFP); Z-Phe-Ala-CHN2; Z-Phe-Phe-CH2F; Z-Phe-Tyr (tBu)-diazomethylketone; Z-Phe-Tyr-aldehyde; a-macroglobulin; and combinations thereof.
25. The method of claim 22 , wherein cathepsin L is inhibited by silencing a gene encoding cathepsin L in cells of the host cell culture.
26. The method of claim 25 , wherein the gene encoding cathepsin L is silenced by one or more molecules selected from: siRNA; miRNA; shRNA; and combinations thereof.