The present invention relates to clinical herpes simplex virus (HSV) isolates with improved oncolytic capabilities as compared to reference laboratory HSV strains. The present invention also relates to methods of producing HSV strains of the invention and to pharmaceutical compositions comprising a HSV strain of the invention.
1. A herpes simplex virus 1 (HSV1) strain, which is modified such that it lacks one or more of a functional ICP34.5-encoding gene, a functional ICP6-encoding gene, a functional glycoprotein H-encoding gene and a functional thymidine kinase-encoding gene, and which is derived from HSV1 strain JS1 as deposited at the European Collection of Cell Cultures (ECACC) under accession number 01010209.
2. An HSV1 strain according to claim 1 , which lacks a functional ICP34.5-encoding gene.
3. An HSV1 strain according to claim 2 , which further lacks a functional ICP47 gene.
4. An HSV1 strain according to claim 1 , which comprises a heterologous gene.
5. An HSV1 strain according to claim 4 , wherein said heterologous gene is a gene capable of modifying immune responses.
6. An HSV1 strain according to claim 5 , wherein said gene capable of modifying immune responses encodes an immune stimulatory polypeptide or another gene product capable of modifying immune responses, a prodrug activator, a tumor suppressor or a pro-apoptotic gene product.
7. An HSV1 strain according to claim 6 , wherein the immune stimulatory polypeptide is granulocyte macrophage colony-stimulating factor (GMCSF), another cytokine or chemokine, RANTES, B7.1 or B7.2 or IL12, wherein the prodrug activator is nitroreductase or cytochrome p45 or wherein the tumor suppressor is p53.
8. An HSV1 strain according to claim 2 , which is modified such that it lacks a functional ICP34.5 gene, and optionally a functional ICP47 gene; and optionally further comprises a heterologous gene encoding GMCSF.
9. A pharmaceutical composition comprising a HSV strain according to claim 1 and a pharmaceutically acceptable carrier or diluent.
10. A method of determining whether a gene enhances the anti-tumor effects of a herpes simplex virus 1 (HSV1) strain comprising:
i. providing an HSV1 according to claim 1 ;
ii. inserting said gene into said HSV1 strain; and
iii. assessing the ability of said modified, oncolytic HSV1 strain to replicate in or kill tumor cells compared to the ability of the precursor strain provided in step (i).