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Updated: May 6, 2026

Generation of a Novel Dendritic-cell Vaccine Using Melanoma and Squamous Cancer Stem Cells
Published on: January 6, 2014
Dendritic cell vaccines targeting survivin in head and neck cancer
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.
Abstract:
Evaluation of: Turksma AW, Bontkes HJ, Ruizendaal JJ et al. Exploring dendritic cell based vaccines targeting survivin for the treatment of head and neck cancer patients. J. Transl. Med. 11, 152-165 (2013). Survivin has been identified to be an inhibitor of apoptosis and is highly expressed in many cancers. A number of strategies have targeted survivin as a novel cancer therapy approach. The evaluated paper makes a number of observations regarding the presence of survivin-specific T cells, as well as attempts for in vitro expansion. The research team has shown that survivin-specific T cells can be measured ex vivo in the peripheral blood of patients with head and neck squamous cell carcinoma by tetramer analysis and from the tumor-draining lymph node of a patient with locally advanced breast cancer by ELIspot analysis. Furthermore, dendritic cells electroporated with survivin and cytokine (i.e., IL-12 and IL-21) mRNA can be used to generate survivin-specific T cells in vitro. However, the enriched or cloned survivin-specific T cells isolated from patients or obtained by in vitro induction could not be maintained for prolonged periods of time. The study team proposed that one explanation for this is fracticide, as activated T cells were shown to express survivin. The evaluated paper therefore concluded that strategies that rely on expansion and adoptive transfer of survivin-specific T cells would not be possible.
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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