Chimeric Newcastle disease viruses and uses thereof
Described herein are chimeric Newcastle disease viruses engineered to express a heterologous interferon antagonist and compositions comprising such viruses. The chimeric Newcastle disease viruses and compositions are useful in the treatment of cancer.
1. A chimeric Newcastle disease virus (NIV), comprising a packaged genome which encodes a heterologous interferon antagonist and a modified F protein with a mutated cleavage site, wherein the heterologous interferon antagonist and the modified F protein are expressed by the virus.
2. The chimeric NDV of claim 1 , wherein the heterologous interferon antagonist is an influenza virus NS1 protein.
3. The chimeric NDV of claim 1 , wherein the heterologous interferon antagonist is Nipah virus W protein, Nipah V protein, Ebola virus VP35 protein, Vaccinia virus E3L, protein, respiratory syncytial virus (RSV)NS2 protein or Hepatitis C virus NS3-4 protease.
4. The chimeric NDV of claim 1 , wherein the packaged genome encodes a tumor antigen, so that the tumor antigen is expressed by the virus.
5. A pharmaceutical composition comprising the chimeric NDV of claim 1 and a pharmaceutically acceptable carrier.
6. A pharmaceutical composition comprising the chinieric NDV of claim 2 and a pharmaceutically acceptable carrier.
7. The chimeric NDV of claim 1 further encoding a cytokine that is expressed by the virus.
8. The chimeric NDV of claim 7 , wherein the cytokine is IL-2.
9. The chimeric NDV of claim 7 , wherein the cytokine is 1 L-15.
10. The chimeric NDV of claim 7 , wherein the cytokine is IL-7, IL-9, IL- 22, or tumor necrosis factor-beta.
11. An isolated cell line comprising the chimeric NDV of claim 1 .
12. An isolated embryonated chicken or quail egg comprising the chimeric NDV of claim 1 .
13. A method for producing a pharmaceutical composition, the method comprising:
(a) propagating the chimeric NDV of claim 1 in a cell line that is susceptible to a NDV infection; and
(b) collecting the progeny virus,
wherein the virus is grown to sufficient quantities and under sufficient conditions that the virus is free from contaraination, such that the progeny virus is suitable for formulation into a pharmaceutical composition.
14. A method for producing a pharmaceutical composition, the method comprising:
(a) propagating the chimeric NDV of claim 1 in an isolated embryonated chicken or quail egg: and
(b) collecting the progeny virus,
wherein the virus is grown to sufficient quantities and under sufficient conditions that the virus is free from contamination, such that the progeny virus is suitable for formulation into a pharmaceutical composition.