In vivo interleukin-2 gene therapy of established tumors with herpes simplex amplicon vectors Journal Article


Authors: D'Angelica, M.; Karpoff, H.; Halterman, M.; Ellis, J.; Klimstra, D.; Edelstein, D.; Brownlee, M.; Federoff, H.; Fong, Y.
Article Title: In vivo interleukin-2 gene therapy of established tumors with herpes simplex amplicon vectors
Abstract: In vivo cytokine gene transfer may greatly simplify autologous tumor vaccine production. Herpes simplex viral amplicon vectors (HSV) are efficient gene-transfer vehicles and may overcome many limitations of prior gene- transfer methods. The interleukin-2 (IL-2) and β-galactosidase genes (lac) were inserted into an HSV amplicon vector and tested in a subcutaneous squamous cell carcinoma of lung origin to determine the efficiency of in vivo gene transfer and the utility of such a direct gene-transfer approach in cancer therapy. Gene transfer and expression were assessed by histochemical staining and enzyme-linked immunosorbent assay (ELISA). Growth of injected tumors as well as non-injected tumors remote from the site of injection was assessed. Assessment of lymphocytic infiltrates into tumors was performed by immunohistochemistry. Survival was recorded. Direct in vivo injection of established tumors with a HSVil2 resulted in efficient gene transfer and production of IL-2 in the injected tumor but not at tumors remote from the sites of injection. There was a significant suppression of growth of the tumors injected with HSVil2 (P < 0.01) when compared with tumors injected with HSV without il2. Of note, growth of tumors remote from sites of HSVi12 injection was also retarded and treatment was associated with a significant (P < 0.05) improvement in survival. Direct intratumoral administration of HSV amplicon vectors can result in efficient transfer of cytokine genes and have antitumor efficacy. HSV vectors are therefore potentially useful agents in such in vivo gene-therapy strategies and simplify cytokine antitumor gene- therapy strategies.
Keywords: immunohistochemistry; controlled study; carcinoma, squamous cell; nonhuman; animals; animal tissue; interleukin 2; lung neoplasms; animal experiment; animal model; tumor cells, cultured; enzyme linked immunosorbent assay; gene transfer; genetic vectors; cancer inhibition; cytokines; immunotherapy; rat; gene therapy; beta galactosidase; simplexvirus; neoplasms, experimental; cytokine production; lung carcinoma; rats; lymphocytic infiltration; herpes simplex virus; interleukin-2; virus vector; rats, inbred f344; beta-galactosidase; dna, recombinant; male; priority journal; article; squamous tumors
Journal Title: Cancer Immunology, Immunotherapy
Volume: 47
Issue: 5
ISSN: 0340-7004
Publisher: Springer  
Date Published: 1999-01-01
Start Page: 265
End Page: 271
Language: English
DOI: 10.1007/s002620050530
PUBMED: 10022470
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 16 August 2016 -- Source: Scopus
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MSK Authors
  1. Howard M Karpoff
    16 Karpoff
  2. David S Klimstra
    978 Klimstra
  3. Yuman Fong
    775 Fong