Literature DB >> 20132058

The evolving role of dendritic cells in cancer therapy.

E J Ilett1, R J D Prestwich, A A Melcher.   

Abstract

IMPORTANCE OF THE FIELD: Dendritic cells (DC) are a clear choice for use in cancer immunotherapy, and much research has focused on generating DC for clinical use. Although DC therapy has been successful in inducing specific anti-tumour immune responses, these have rarely translated into clinical efficacy. AREAS COVERED IN THIS REVIEW: We examine some of the components of generating DC for therapy, including their culture, antigen loading and delivery, and discuss why DC therapy has not yet delivered substantial clinical benefit. We also examine more novel approaches, such as the potential for combination DC-based immunomodulatory strategies. WHAT THE READER WILL GAIN: Given the highly immunosuppressive tumour environment, many of the approaches to DC vaccination are unlikely to result in effective therapy, as even successfully primed T cells may fail to infiltrate tumours or be anergized after entry. Broader approaches against multiple tumour-associated antigens in the context of overcoming tumour immune suppression are likely to prove more successful. The combination of oncolytic viral therapy with DC vaccines may promote an inflammatory tumour environment, inducing optimal DC activation, T cell priming and effective therapy. TAKE HOME MESSAGE: Evolving DC-based therapeutic strategies addressing multiple components of tumour-immune system interactions may yield substantial benefits for patients.

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Year:  2010        PMID: 20132058     DOI: 10.1517/14712590903559830

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  14 in total

Review 1.  Thunder and lightning: immunotherapy and oncolytic viruses collide.

Authors:  Alan Melcher; Kelley Parato; Cliona M Rooney; John C Bell
Journal:  Mol Ther       Date:  2011-04-19       Impact factor: 11.454

Review 2.  The characterization and role of leukemia cell-derived dendritic cells in immunotherapy for leukemic diseases.

Authors:  Changjin Yuan; Guanhua Song; Guosheng Jiang
Journal:  Intractable Rare Dis Res       Date:  2012-05

3.  Administration of a vaccine composed of dendritic cells pulsed with premalignant oral lesion lysate to mice bearing carcinogen-induced premalignant oral lesions stimulates a protective immune response.

Authors:  Anna-Maria A De Costa; Danielle N Justis; Corinne A Schuyler; M Rita I Young
Journal:  Int Immunopharmacol       Date:  2012-05-16       Impact factor: 4.932

4.  Virus-induced tumor inflammation facilitates effective DC cancer immunotherapy in a Treg-dependent manner in mice.

Authors:  Norman Woller; Sarah Knocke; Bettina Mundt; Engin Gürlevik; Nina Strüver; Arnold Kloos; Bita Boozari; Peter Schache; Michael P Manns; Nisar P Malek; Tim Sparwasser; Lars Zender; Thomas C Wirth; Stefan Kubicka; Florian Kühnel
Journal:  J Clin Invest       Date:  2011-06-06       Impact factor: 14.808

5.  Generation of induced pluripotent stem cells from mouse cancer cells.

Authors:  Frances Ka-Yin Lin; Yiu-Loon Chui
Journal:  Cancer Biother Radiopharm       Date:  2012-08-14       Impact factor: 3.099

6.  Hypomorphic mutation in the site-1 protease Mbtps1 endows resistance to persistent viral infection in a cell-specific manner.

Authors:  Daniel L Popkin; John R Teijaro; Brian M Sullivan; Shuzo Urata; Sophie Rutschmann; Juan Carlos de la Torre; Stefan Kunz; Bruce Beutler; Michael Oldstone
Journal:  Cell Host Microbe       Date:  2011-03-17       Impact factor: 21.023

Review 7.  Immunomodulatory effects of dsRNA and its potential as vaccine adjuvant.

Authors:  Bo Jin; Tao Sun; Xiao-Hong Yu; Chao-Qun Liu; Ying-Xiang Yang; Ping Lu; Shan-Feng Fu; Hui-Bin Qiu; Anthony E T Yeo
Journal:  J Biomed Biotechnol       Date:  2010-07-05

8.  Enhanced cross-priming of naive CD8+ T cells by dendritic cells treated by the IMiDs® immunomodulatory compounds lenalidomide and pomalidomide.

Authors:  Jake Y Henry; Marie-Christine Labarthe; Brendan Meyer; Prokar Dasgupta; Angus G Dalgleish; Christine Galustian
Journal:  Immunology       Date:  2013-07       Impact factor: 7.397

9.  The immunosuppressive factors IL-10, TGF-β, and VEGF do not affect the antigen-presenting function of CD40-activated B cells.

Authors:  Alexander Shimabukuro-Vornhagen; Andreas Draube; Tanja M Liebig; Achim Rothe; Matthias Kochanek; Michael S von Bergwelt-Baildon
Journal:  J Exp Clin Cancer Res       Date:  2012-05-16

10.  Trends in cancer immunotherapy.

Authors:  Joseph F Murphy
Journal:  Clin Med Insights Oncol       Date:  2010-07-14
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