Compositions, methods and uses for treating solid tumors using LCMV-GP-VSV pseudotype vectors
Embodiments of the present invention relate to compositions and methods for producing recombinant VSV viruses. In accordance with these embodiments, viral vectors can include a glycoprotein GP of the lymphocyte choriomeningitis virus (LCMV) instead of the G protein of the VSV. Other embodiments relate to cells for producing a LCMV-GP-pseudotyped VSV vectors. Embodiments also relate to the use of the vectors and cells as part of a pharmaceutical composition for the treatment of solid tumors.
1. A method for treating a subject having one or more solid tumors, the method comprising:
administering to the subject, a pharmaceutical composition comprising a therapeutically effective amount of a tumor-specific replication competent Vesicular stomatitis virus (VSV) pseudotyped vector having a gene encoding a glycoprotein (GP) of lymphocytic choriomeningitis virus (LCMV) (VSV-LCMV-GP pseudotype vector) and the vector either lacks a functional gene coding for envelope protein G of VSV or the envelope protein G is replaced;
wherein infection of cells with the replication competent VSV-LCMV-GP pseudotyped vector causes LCMV-GP to be encoded in the genome of progeny viral particle and subsequently expressed on the surface of the progeny viral particle and wherein tropism of the progeny viral particles is independent of an additional tumor-targeting element or transgene in the VSV-LCMV-GP pseudotype vector and wherein the progeny viral particle exhibits tumor-specific replication competence;
wherein the one or more solid tumors is selected from the group consisting of a reproductive tumor, an ovarian tumor, a testicular tumor, an endocrine tumor, a gastrointestinal tumor, a liver tumor, a kidney tumor, a colon tumor, a colorectal tumor, a bladder tumor, a prostate tumor, a skin tumor, melanoma, a respiratory tumor, a lung tumor, a breast tumor and a bone tumor; and
wherein the pharmaceutical composition comprises a pharmaceutically acceptable carrier or excipient and wherein the pharmaceutical composition treats the solid tumor in the subject.
2. The method of claim 1 , wherein the pharmaceutical composition comprising the VSV-LCMV-GP pseudotyped vector is administered to the subject using at least one intravenous administration.
3. The method of claim 1 , wherein the pharmaceutical composition comprising the VSV-LCMV-GP pseudotyped vector is administered to the subject using at least one intratumoral administration.
4. The method of claim 1 , wherein the pharmaceutical composition comprising the VSV-LCMV-GP pseudotyped vector is administered to the subject at a dose ranging from 1×10 5 to 1×10 15 plaque forming units (PFU).
5. The method of claim 1 , wherein the administering to the subject a pharmaceutical composition further comprises contacting directly the one or more solid tumors with a therapeutically effective amount of the VSV-LCMV-GP pseudotyped vector.
6. The method of claim 1 , wherein the pharmaceutical composition comprises one or more cells capable of producing the therapeutically effective amount of the VSV-LCMV-GP pseudotyped vector.
7. The method of claim 6 , wherein the one or more cells comprises a multipotent adult progenitor cell (MAPC), a neuronal stem cell (NSC), a mesenchymal stem cell (MSC), a bone marrow derived tumor infiltrating cell (BM-TIC cells), or a combination thereof.
8. The method of claim 1 , wherein the VSV-LCMV-GP pseudotyped vector further comprises one or more transgenes.
9. The method of claim 8 , wherein the one or more transgenes encodes at least one of a suicide protein, an immunostimulatory protein, a marker protein, or a combination thereof.
10. The method of claim 8 , wherein the one or more transgenes encodes at least one of thymidine kinase of the herpes simplex virus (HSV-TK), cytosine deaminase, FKBP-FAS, or FKBP-caspase-9.
11. The method of claim 8 , wherein the one or more transgenes encodes at least one of interleukin-2 (IL-2), IL-4, IL-12, neutralizing anti-TGFbeta, or Flt3L or combination thereof.
12. The method of claim 1 , wherein the pharmaceutical composition further comprises an anti-tumor agent.
13. The method of claim 12 , wherein the anti-tumor agent comprises a chemotherapy drug, a platinum complex, a mitotic inhibitor, an alkylating agent, an anti-metabolite, an anti-tumor antibiotic, a DNA topoisomerase inhibitor, or a combination thereof.
14. A method of treating melanoma in a subject, the method comprising:
administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a replication competent Vesicular stomatitis virus (VSV) pseudotyped vector having a gene encoding the envelope glycoprotein (GP of the lymphocytic choriomeningitis virus (LCMV) as a replacement for endogenous glycoprotein G of the VSV pseudotyped vector,
wherein the pharmaceutical composition comprises a pharmaceutically acceptable carrier or excipient, and
wherein the pharmaceutical composition treats the melanoma in the subject.
15. The method of claim 14 , wherein the pharmaceutical composition comprising the VSV-LCMV-GP pseudotyped vector is administered to the subject at a dose ranging between about 1×10 5 to about 1×10 15 PFU.
16. A method of treating ovarian cancer in a subject, the method comprising:
administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a replication competent Vesicular stomatitis virus (VSV) pseudotyped vector having a gene encoding the envelope glycoprotein (GP) of the lymphocytic choriomeningitis virus (LCMV) as a replacement for endogenous glycoprotein G of the VSV pseudotyped vector,
wherein the pharmaceutical composition comprises a pharmaceutically acceptable carrier or excipient, and
wherein the pharmaceutical composition treats the ovarian cancer in the subject.
17. The method of claim 16 , wherein the pharmaceutical composition comprising the VSV-LCMV-GP pseudotyped vector is administered to the subject at a dose ranging from 1×10 3 to 1×10 10 PFU.
18. The method of claim 16 , wherein the pharmaceutical composition further comprises an anti-tumor agent.
19. A method of treating prostate cancer in a subject, the method comprising:
administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a replication competent Vesicular stomatitis virus (VSV) pseudotyped vector having a gene encoding the envelope glycoprotein (GP) of the lymphocytic choriomeningitis virus (LCMV) as a replacement for endogenous glycoprotein G of the VSV pseudotyped vector,
wherein the pharmaceutical composition comprises a pharmaceutically acceptable carrier or excipient, and
wherein the pharmaceutical composition treats the prostate cancer in the subject.
20. The method of claim 19 , wherein the pharmaceutical composition comprising the VSV-LCMV-GP pseudotyped vector is administered to the subject at a dose ranging from 1×10 3 to 1×10 10 PFU.
21. The method of claim 1 , wherein the glycoprotein GP of the VSV-LCMV-GP pseudotyped vector is unmutated.
22. A method for treating a subject having a glioblastoma, the method comprising:
administering to the subject, a pharmaceutical composition comprising a therapeutically effective amount of a tumor-specific replication competent Vesicular stomatitis virus (VSV) pseudotyped vector having a gene encoding a glycoprotein (GP) of lymphocytic choriomeningitis virus (LCMV) (VSV-LCMV-GP pseudotype vector) and the vector either lacks a functional gene coding for envelope protein G of VSV or the envelope protein G is replaced;
wherein infection of cells with the replication competent VSV-LCMV-GP pseudotyped vector causes LCMV-GP to be encoded in the genome of progeny viral particle and subsequently expressed on the surface of the progeny viral particle and wherein tropism of the progeny viral particles is independent of an additional tumor-targeting element or transgene in the VSV-LCMV-GP pseudotype vector and wherein the progeny viral particle exhibits tumor-specific replication competence;
wherein the pharmaceutical composition comprises a pharmaceutically acceptable carrier or excipient and wherein the pharmaceutical composition treats the glioblastoma in the subject.
23. The method of claim 1 , wherein the one or more solid tumors is selected from the group consisting of an ovarian tumor, a colon tumor, a prostate tumor, a melanoma, or a lung tumor.