GENETICALLY MODIFIED NK-92 CELL LINE
This invention is directed to treatment of a subject having or suspected of having a cancer comprising administering to the subject a monoclonal antibody and NK-92 expressing Fc receptor.
1 . An NK-92 cell line comprising NK-92 cells genetically modified to comprise a bicistronic expression construct, wherein the bicistronic expression construct comprises, in the 5′ to 3′ direction, a polynucleotide encoding a CD16 polypeptide having a valine at position 158 of the mature form of the CD16 polypeptide, and a polynucleotide encoding an interleukin-2 (IL-2) polypeptide targeted to the endoplasmic reticulum (ER).
2 . The NK-92 cell line of claim 1 , wherein the bicistronic expression construct is encoded by a plasmid vector.
3 . The NK-92 cell line of claim 1 , wherein the CD16 polypeptide has at least 90% identity to SEQ ID NO:2.
4 . The NK-92 cell line of claim 1 , wherein the CD16 polypeptide has at least 95% identity to SEQ ID NO:2.
5 . The NK-92 cell line of claim 1 , wherein the CD16 polypeptide comprises SEQ ID NO:2
6 . The NK-92 cell line of claim 1 , wherein the IL-2 polypeptide targeted to the ER has at least 90% identity to SEQ ID NO:7.
7 . The NK-92 cell line of claim 1 , wherein the IL-2 polypeptide targeted to the ER has at least 95% identity to SEQ ID NO:7.
8 . The NK-92 cell line of claim 1 , wherein the IL-2 polypeptide targeted to the ER comprises SEQ ID NO:7.
9 . The NK-92 cell lines of claim 1 , wherein the CD16 polypeptide has at least 90% identity to SEQ ID NO:2; and the IL-2 polypeptide targeted to the ER has at least 90% identity to SEQ ID NO:7.
10 . The NK-92 cell lines of claim 1 , wherein the CD16 polypeptide has at least 95% identity to SEQ ID NO:2; and the IL-2 polypeptide targeted to the ER has at least 95% identity to SEQ ID NO:7.
11 . The NK-92 cell lines of claim 1 , wherein the CD16 polypeptide comprises SEQ ID NO:2; and the IL-2 polypeptide targeted to the ER comprises SEQ ID NO: 7.
12 . The NK-92 cell line of claim 1 , wherein the NK-92 cells further comprise a genetic modification to express a safety system gene that allows the NK-92 cells to be killed by introduction of a selective agent.
13 . The NK-92 cell line of claim 1 , wherein the safety system gene is selected from the group consisting of an inducible caspase 9 gene, a thymidine kinase gene, a cytosine deaminase gene, a cytochrome p450 gene, a nitroreductase gene, an Escherichia coli gpt gene, and an Escherichia coli deo gene.
14 . The NK-92 cell line of claim 1 , wherein the safety system gene is a mutant thymidine kinase gene selected from the group consisting of tk30, tk75, and sr39tk.
15 . The NK-92 cell line of claim 1 , wherein the safety system gene is a wildtype thymidine kinase gene.