Abstract
The behaviour of circulating dendritic cells (DCs) and DC generation from monocytes in melanoma patients during the progression of disease have not been described. We report a significant decrease in the absolute number of total DCs, which mainly affects plasmacytoid DCs in stage IV. Additionally, monocyte-DC generation is less efficient in advanced stages, resulting in DCs that exhibit increased phagocytic capacity, potentially indicating a less mature state. These findings elucidate aspects of basic tumour-mediated immunosuppression, which may have implications for immunotherapeutic approaches, suggesting that the selection of patients for immunotherapy should also be made on the basis of their immune status.
Keywords:
Circulating dendritic cells; Generation of dendritic cells; Immunotherapy; Melanoma.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Case-Control Studies
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Cell Count
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Cell Shape
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Cells, Cultured
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Coculture Techniques
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Dendritic Cells / immunology*
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Dendritic Cells / metabolism
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Dendritic Cells / pathology
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Dextrans / metabolism
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Disease Progression
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Down-Regulation
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Endocytosis
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Female
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Fluorescein-5-isothiocyanate / analogs & derivatives
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Fluorescein-5-isothiocyanate / metabolism
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Humans
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Immunotherapy
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Lectins, C-Type / metabolism
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Lymphocyte Activation
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Lymphocyte Culture Test, Mixed
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Male
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Mannose Receptor
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Mannose-Binding Lectins / metabolism
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Melanoma / immunology*
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Melanoma / secondary
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Melanoma / therapy
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Middle Aged
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Monocytes / immunology*
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Monocytes / metabolism
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Monocytes / pathology
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Neoplasm Staging
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Phagocytosis
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Phenotype
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Receptors, Cell Surface / metabolism
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Skin Neoplasms / immunology*
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Skin Neoplasms / pathology
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Skin Neoplasms / therapy
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T-Lymphocytes / immunology
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Time Factors
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Tumor Escape
Substances
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Dextrans
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Lectins, C-Type
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Mannose Receptor
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Mannose-Binding Lectins
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Receptors, Cell Surface
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fluorescein isothiocyanate dextran
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Fluorescein-5-isothiocyanate