Lentiviral packaging constructs
The present invention provides novel lentiviral packaging constructs that are useful for the establishment of stable packaging cell lines and producer cell lines. In particular, the present invention provides novel packaging cell lines that are capable of constitutively expressing high levels of lentiviral proteins.
1. A method for producing a recombinant lentiviral vector particle preparation comprising the steps of:
transfecting a packaging cell line comprising a packaging construct comprising a sequence encoding a lentiviral protease containing a substitution where T is replaced with S in the DTGAD motif (SEQ ID NO: 1) and a deletion in a lentiviral packaging signal sequence with a lentiviral vector,
propagating the cell line in a suitable culture medium and
obtaining a recombinant lentiviral vector particles preparation from said culture medium.
2. The method of claim 1 , wherein said sequence encoding said protease comprises a lentiviral pol gene.
3. The method of claim 2 , further comprising a lentiviral gag gene.
4. The method of claim 1 wherein said lentiviral protease is an HIV protease.
5. The method of claim 1 wherein said lentiviral protease is a BIV protease.
6. The method of claim 1 wherein said lentiviral protease is an EIAV protease.
7. The method of claim 1 wherein said lentiviral protease is an SIV protease.
8. The method of claim 1 wherein said lentiviral protease is an FIV protease.
9. The method of claim 1 wherein expression of the lentiviral protease gene is constitutive.
10. The method of claim 1 wherein said cell line further comprises an env gene.
11. The method of claim 1 , 2 or 3 , wherein said sequence encoding a lentiviral protease is obtained from HIV genome.
12. The method of claim 1 , 2 or 3 , wherein said sequence encoding a lentiviral protease is obtained from BIV genome.
13. The method of claim 1 wherein expression of the lentiviral gag gene is constitutive.
14. The method of claim 2 or 3 wherein expression of the lentiviral pol gene is constitutive.
15. The method of claim 11 further comprising a deletion of, or mutation in, a vif gene, a vpr gene or both.
16. The method of claim 12 further comprising a deletion of, or mutation in, one or more of a vif gene, a W gene, a Y gene or a Tat gene.
17. The method of claim 1 or 10 , wherein said cell line further comprises a rev gene.