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Tractable In Vivo Reprogramming of Tumor Cells to Type 1 Conventional Dendritic Cell-like Cells
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Immunosuppressive mechanisms of regulatory dendritic cells in cancer

Galina V Shurin1, Yang Ma, Michael R Shurin

  • 1Division of Experimental Pathology, Department of Pathology, University of Pittsburgh Medical Center, Scaife Hall S733 3550 Terrace Street, Pittsburgh, PA, 15261, USA, shuringv@upmc.edu.

Cancer Microenvironment : Official Journal of the International Cancer Microenvironment Society
|June 11, 2013
PubMed

Three major functional subsets of dendritic cells (DCs) have been described in the tumor microenvironment in patients with cancer and tumor-bearing animals: (i) conventional DCs with intact antigen-presenting capabilities, (ii) functionally defective DCs with decreased motility and low ability to uptake, process and present antigens or produce cytokines and (iii) regulatory DCs with high capacity to suppress T cell proliferation, induce differentiation of regulatory T cells or support immune tolerance. Phenotypic characteristics of regulatory DCs (regDCs), as well as the mechanisms of T cell inhibition, vary in different experimental conditions and environments, suggesting high level of their plasticity and probably different origin. Although new data demonstrate that regDCs may play an important role at early stages of tumor development, functional differences and clinical significance of emergence of different myeloid regulatory cells (MDSCs, regDCs, M2 macrophages, N2 neutrophils, mast cells) in cancer remain to be determined.

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