Genetically Modified Dendritic Cells in Cancer Immunotherapy

  • Brian J. Morrison
  • Jason C. Steel
  • Melissa Gregory
  • John C. Morris
  • Anatoli M. MalyguineEmail author


Dendritic cells are powerful antigen-presenting cells that can generate primary cytolytic T lymphocyte responses against tumors. Consequently, there has been much interest in their application as antitumor vaccines. A number of dendritic cell-based vaccine trials targeting a variety of tumors have been conducted in different countries; however, the rate of clinical responses remains low. The majority of these studies have administered dendritic cells loaded with synthetic peptide epitopes or tumor lysates. Genetic modification of dendritic cells to express tumor antigens or immunostimulatory molecules through gene transfer or mRNA transfection offers a logical alternative with potential advantages over antigen loading in dendritic cells. In this chapter, we review the current and future prospects for genetically modified dendritic cell vaccines for cancer therapy.


Programme Death Ligand Dendritic Cell Vaccine Antitumor Vaccine Immunostimulatory Molecule Semliki Forest Virus Vector 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.



This research was supported by the Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research.

This project has been funded in whole or in part with federal funds from the National Cancer Institute, National Institutes of Health, under contract no. N01-CO-12400. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products or organizations imply endorsement by the US Government.


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Copyright information

© Springer Science+Business Media, LLC 2009

Authors and Affiliations

  • Brian J. Morrison
  • Jason C. Steel
  • Melissa Gregory
  • John C. Morris
  • Anatoli M. Malyguine
    • 1
    Email author
  1. 1.Laboratory of Cell Mediated Immunity, CSP, SAIC-Frederick, IncNational Cancer Institute at FrederickFrederickUSA

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