Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Apr 11:5:165.
doi: 10.3389/fimmu.2014.00165. eCollection 2014.

Paradigm Shift in Dendritic Cell-Based Immunotherapy: From in vitro Generated Monocyte-Derived DCs to Naturally Circulating DC Subsets

Affiliations
Review

Paradigm Shift in Dendritic Cell-Based Immunotherapy: From in vitro Generated Monocyte-Derived DCs to Naturally Circulating DC Subsets

Florian Wimmers et al. Front Immunol. .

Abstract

Dendritic cell (DC)-based immunotherapy employs the patients' immune system to fight neoplastic lesions spread over the entire body. This makes it an important therapy option for patients suffering from metastatic melanoma, which is often resistant to chemotherapy. However, conventional cellular vaccination approaches, based on monocyte-derived DCs (moDCs), only achieved modest response rates despite continued optimization of various vaccination parameters. In addition, the generation of moDCs requires extensive ex vivo culturing conceivably hampering the immunogenicity of the vaccine. Recent studies, thus, focused on vaccines that make use of primary DCs. Though rare in the blood, these naturally circulating DCs can be readily isolated and activated thereby circumventing lengthy ex vivo culture periods. The first clinical trials not only showed increased survival rates but also the induction of diversified anti-cancer immune responses. Upcoming treatment paradigms aim to include several primary DC subsets in a single vaccine as pre-clinical studies identified synergistic effects between various antigen-presenting cells.

Keywords: dendritic cell vaccination; immunotherapy; melanoma; monocyte-derived dendritic cells; myeloid dendritic cells; naturally circulating dendritic cells; plasmacytoid dendritic cells.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Development of DC-based immunotherapy against melanoma.
Figure 2
Figure 2
Biology of immunotherapy-relevant human DC subsets. Depicted are major DC functions relevant for pathogen recognition and DC activation, T cell priming, and anti-cancer immunity.

References

    1. Maio M. Melanoma as a model tumour for immuno-oncology. Ann Oncol (2012) 23(Suppl 8):viii10–410.1093/annonc/mds257 - DOI - PubMed
    1. Ferlay J, Soerjomataram I, Ervik M, Dikshit R, Eser S, Mathers C, et al. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11 [Web Page]. Lyon: International Agency for Research on Cancer; (2012).
    1. Dennis LK. Analysis of the melanoma epidemic, both apparent and real: data from the 1973 through 1994 surveillance, epidemiology, and end results program registry. Arch Dermatol (1999) 135(3):275–8010.1001/archderm.135.3.275 - DOI - PubMed
    1. de Vries E, Coebergh JW. Melanoma incidence has risen in Europe. BMJ (2005) 331(7518):698.10.1136/bmj.331.7518.698 - DOI - PMC - PubMed
    1. Balch CM, Gershenwald JE, Soong SJ, Thompson JF, Atkins MB, Byrd DR, et al. Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol (2009) 27(36):6199–20610.1200/JCO.2009.23.4799 - DOI - PMC - PubMed