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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
  • University College Cork
  • University of East Anglia, Norwich Medical School

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

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
StatePublished - Aug 2014
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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