Dendritic cell vaccines targeting survivin in head and neck cancer

Walter T Lee1

  • 1Section of Otolaryngology, Head & Neck Surgery, Veteran Affairs Medical Center, Durham, NC 27705, USA and Division of Otolaryngology, Head & Neck Surgery, Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA. walter.lee@duke.edu.

Immunotherapy
|November 6, 2013
PubMed

Insights

Survivin-targeted cancer vaccines show promise but face challenges. While survivin-specific T cells can be generated, their prolonged survival for adoptive transfer is hindered by fracticide, limiting current therapeutic strategies.

Area of Science:

  • Immunology
  • Oncology
  • Cancer Therapy

Background:

  • Survivin, an apoptosis inhibitor, is highly expressed in various cancers, making it a target for novel cancer therapies.
  • Head and neck squamous cell carcinoma (HNSCC) and other cancers often exhibit high survivin expression.

Purpose of the Study:

  • To explore dendritic cell-based vaccines targeting survivin for head and neck cancer treatment.
  • To investigate the presence and expansion of survivin-specific T cells in cancer patients.

Main Methods:

  • Tetramer analysis of peripheral blood from HNSCC patients.
  • ELIspot analysis of tumor-draining lymph nodes.
  • In vitro generation of survivin-specific T cells using dendritic cells electroporated with survivin and cytokine mRNA (IL-12, IL-21).

Main Results:

  • Survivin-specific T cells were detected ex vivo in HNSCC patients.
  • Dendritic cells could generate survivin-specific T cells in vitro.
  • Prolonged maintenance of expanded or cloned survivin-specific T cells was not achieved.
  • Activated T cells expressed survivin, suggesting fracticide as a limiting factor.

Conclusions:

  • Adoptive transfer strategies relying on the expansion of survivin-specific T cells are currently not feasible.
  • Further research is needed to overcome challenges like fracticide in survivin-targeted immunotherapy.

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