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Genetically modified dendritic cells in cancer immunotherapy: a better tomorrow?

  1. Author:
    Shurin, M. R.
    Gregory, M.
    Morris, J. C.
    Malyguine, A. M.
  2. Author Address

    [Gregory, Melissa; Malyguine, Anatoli M.] NCI, Appl & Dev Res Support Program, SAIC Frederick Inc, Frederick, MD 21702 USA. [Shurin, Michael R.] Univ Pittsburgh, Dept Pathol, Med Ctr, Pittsburgh, PA USA. [Shurin, Michael R.] Univ Pittsburgh, Dept Immunol, Med Ctr, Pittsburgh, PA USA. [Morris, John C.] NCI, Ctr Canc Res, Metab Branch, Bethesda, MD 20892 USA.;Malyguine, AM, NCI, Appl & Dev Res Support Program, SAIC Frederick Inc, Bldg 560 Room 12-79, Frederick, MD 21702 USA.;malyguinea@mail.nih.gov
    1. Year: 2010
    2. Date: Nov
  1. Journal: Expert Opinion on Biological Therapy
    1. 10
    2. 11
    3. Pages: 1539-1553
  2. Type of Article: Review
  3. ISSN: 1471-2598
  1. Abstract:

    Importance of the field: Dendritic cells (DC) are powerful antigen-presenting cells that induce and maintain primary cytotoxic T lymphocyte (CTL) responses directed against tumor antigens. Consequently, there has been much interest in their application as antitumor vaccines. Areas covered in this review: A large number of DC-based vaccine trials targeting a variety of cancers have been conducted; however, the rate of reported clinically significant responses remains low. Modification of DC to express tumor antigens or immunostimulatory molecules through the transfer of genes or mRNA transfection offers a logical alternative with potential advantages over peptide- or protein antigen-loaded DC. In this article, we review the current results and future prospects for genetically modified DC vaccines for the treatment of cancer. What the reader will gain: Genetically-modified dendritic cell-based vaccines represent a powerful tool for cancer therapy. Numerous preclinical and clinical studies have demonstrated the potential of dendritic cell vaccines alone or in combination with other therapeutic modalities. Take home message: Genetically modified DC-based anti-cancer vaccination holds promise, perhaps being best employed in the adjuvant setting with minimal residual disease after primary therapy, or in combination with other antitumor or immune-enhancing therapies.

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External Sources

  1. DOI: 10.1517/14712598.2010.526105
  2. WOS: 000283132400004

Library Notes

  1. Fiscal Year: FY2010-2011
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