Enhancement of electroporation facilitated immunogene therapy via T-reg depletion

  • P. F. Forde
  • , M. Sadadcharam
  • , L. J. Hall
  • , T. R. O'Donovan
  • , M. De Kruijf
  • , W. L. Byrne
  • , G. C. O'Sullivan
  • , D. M. Soden

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Regulatory T cells (T-regs) can negatively impact tumor antigen-specific immune responses after infiltration into tumor tissue. However, depletion of T-regs can facilitate enhanced anti-tumor responses, thus augmenting the potential for immunotherapies. Here we focus on treating a highly aggressive form of cancer using a murine melanoma model with a poor prognosis. We utilize a combination of T-reg depletion and immunotherapy plasmid DNA delivered into the B16F10 melanoma tumor model via electroporation. Plasmids encoding murine granulocyte macrophage colony-stimulating factor and human B71 were transfected with electroporation into the tumor and transient elimination of T-regs was achieved with CD25-depleting antibodies (PC61). The combinational treatment effectively depleted T-regs compared to the untreated tumor and significantly reduced lung metastases. The combination treatment was not effective in increasing the survival, but only effective in suppression of metastases. These results indicate the potential for combining T-reg depletion with immunotherapy-based gene electrotransfer to decrease systemic metastasis and potentially enhance survival.

    Original languageEnglish
    Pages (from-to)349-354
    Number of pages6
    JournalCancer Gene Therapy
    Volume21
    Issue number8
    DOIs
    Publication statusPublished - Aug 2014

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