US2007166287A1PendingUtilityA1
Oncolytic virus
Est. expirySep 17, 2019(expired)· nominal 20-yr term from priority
Inventors:John BellNahum SonenbergDavid F. StojdlEarl BrownHarold AtkinsRicardo MariusBrian LichtyShane Knowles
C12N 2760/20251C12N 2760/20232C07K 14/005C12N 2810/6081C12N 7/00A61K 38/21C12N 2760/20222A61K 48/00A61K 35/766C12N 15/86
57
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Abstract
The present invention is directed to a method of reducing the viability of a tumor cell involving administering a virus that is not a common human pathogen to the tumor cell. Preferably, the virus exhibits differential susceptibility, in that normal cells are not affected by the virus. This differential susceptibility is more pronounced in the presence of interferon. The tumor cell is characterized by having low levels, or no, PKR activity, or as being PKR−/−, STAT1−/− or both PKR−/− and STAT1−/−. The virus is selected from the group consisting of Rhabdovirus and picomavirus, and preferably is vesicular stomatitis virus (VSV) or a derivative thereof.
Claims
exact text as granted — not AI-modified1 . A method of reducing the viability of a tumor cell, comprising administering to the tumor cell an attenuated strain of vesicular stomatitis virus, wherein said tumor cell is a carcinoma.
2 . The method of claim 1 , wherein the carcinoma is a lung carcinoma.
3 . The method of claim 1 , wherein the tumor cell is PKR−/−; STAT1−/−; or both PKR−/− and STAT1−/−.
4 . The method of claim 1 , wherein the virus is unable to inactivate PKR activity within the tumor cell.
5 . The method of claim 1 , wherein the virus is vesicular stomatitis virus strain M1.
6 . The method of claim 1 , wherein the virus is vesicular stomatitis virus strain M2.
7 . The method of claim 1 , wherein the virus is vesicular stomatitis virus strain M3.
8 . The method of claim 1 , wherein the virus is vesicular stomatitis virus strain M4.
9 . The method of claim 1 , wherein the virus is vesicular stomatitis virus strain M5.
10 . The method of claim 1 , wherein the tumor cell is in a mammalian subject and the virus is administered to the tumor cell by intravenous, intranasal, intraperitoneal or intratumoral administration to the subject.
11 . The method of claim 10 , wherein the mammalian subject is a human or a non-human mammal.
12 . The method of claim 10 , wherein the virus is contained in cell line infected with the virus and the administration comprises administering the virus-infected cell line to the subject by a route selected from intratumorally, intravenously or intraperitoneally.
13 . A method of reducing the viability of a tumor cell within a population of tumor cells and non-tumor cells comprising administering an attenuated strain of vesicular stomatitis virus to the population of cells, wherein tumor cells are carcinoma cells and the virus is able to selectively infect and kill the tumor cell.
14 . The method of claim 13 , wherein the virus is unable to inactivate PKR activity in the tumor cell.
15 . The method of claim 14 , further comprising treating the population of cells with interferon prior to administering the virus.Cited by (0)
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