Microorganisms for therapy
Therapeutic methods and vaccinia virus therefor are provided. The viruses are designed so that they accumulate in immunoprivileged tissues and cells, such as in tumors and other proliferating tissue and in inflamed tissues, compared to other tissues, cells and organs, so that they exhibit relatively low toxicity to host organisms. Combinations of the viruses and anti-cancer agents and uses thereof for treating cancer also are provided.
1. A recombinant vaccinia virus, comprising a modified thymidine kinase (TK) gene and a modified hemagglutinin (HA) gene, and an insertion, deletion or mutation in the gene or locus designated F3, wherein:
each of the TK, HA and F3 gene or locus is inactivated; and
the F3 locus occurs on the HindIII-F fragment of the vaccinia virus between open reading frames F14L and F15L.
2. The recombinant vaccinia virus of claim 1 , wherein heterologous nucleic acid is inserted into the TK and HA genes to inactivate them, and heterologous nucleic acid is inserted into the F3 locus.
3. The recombinant vaccinia virus of claim 1 , wherein the vaccinia virus is a strain selected from among Western Reserve (WR), Copenhagen, Tashkent, Tian Tan, Lister, Wyeth, IHD-J, and IHD-W, Ankara, MVA, Dairen I, L-IPV, LC16M8, LC16MO, LIVP, WR 65-16, Connaught and New York City Board of Health.
4. The recombinant vaccinia virus of claim 1 , wherein the insertion in the F3 locus is at a site corresponding to the unique NotI or position 1475 of the LIVP strain inside of the HindIII-F fragment of the LIVP strain of vaccinia virus.
5. The recombinant vaccinia virus of claim 1 , wherein at least one of the TK, HA gene and F3 locus comprises an insertion of heterologous nucleic acid that encodes a protein.
6. The recombinant vaccinia virus of claim 5 , wherein the protein is an antibody or antigen-binding fragment thereof.
7. The recombinant vaccinia virus of claim 5 , wherein the protein is a solute carrier protein (sic), a superoxide dismutase (sod), a colony stimulating factor (csf), monocyte chemotactic protein-1 (mcp-1), a nonmetastatic protein (nm), a neurogenin protein (ngn), erythropoietin (epo), bmp2, bmp2a, bmp4, tyre 1, tyrp2 or aim 1.
8. The recombinant vaccinia virus of claim 7 , wherein the protein is an slc selected from among solute carrier 5 (slc5) and solute carrier 6 (slc6) transporter protein families.
9. The recombinant vaccinia virus of claim 8 , wherein the transporter protein is a norepinephrine transporter (net) or is a sodium-iodide symporter (nis).
10. The recombinant vaccinia virus of claim 5 , wherein the heterologous nucleic acid is operatively linked to a regulatory sequence.
11. The recombinant vaccinia virus of claim 10 , wherein the regulatory sequence comprises a promoter.
12. The recombinant vaccinia virus of claim 10 , wherein the regulatory sequence comprises the vaccinia virus early/late promoter p7.5.
13. The recombinant vaccinia virus of claim 10 , wherein the regulatory sequence comprises an early/late vaccinia pE/L promoter.
14. The recombinant vaccinia virus of claim 5 , wherein heterologous nucleic acid encodes a detectable protein or a protein capable of inducing a detectable signal.
15. The recombinant vaccinia virus of claim 5 , wherein the encoded protein is an anti-tumor agent or an anti-metastatic agent.
16. A pharmaceutical composition, comprising the virus of claim 1 .
17. The pharmaceutical composition of claim 16 that is formulated for systemic administration.
18. The pharmaceutical composition of claim 16 that is formulated for intravenous administration.
19. A combination, comprising:
a recombinant vaccinia virus of claim 1 ; and
a chemotherapeutic or anti-tumor agent.