TY - JOUR
T1 - Cytotoxic dendritic cells generated from cancer patients
AU - Lakomy, Daniela
AU - Janikashvili, Nona
AU - Fraszczak, Jennifer
AU - Trad, Malika
AU - Audia, Sylvain
AU - Samson, Maxime
AU - Ciudad, Marion
AU - Vinit, Julien
AU - Vergely, Catherine
AU - Caillot, Denis
AU - Foucher, Pascal
AU - Lagrost, Laurent
AU - Chouaib, Salem
AU - Katsanis, Emmanuel
AU - Larmonier, Nicolas
AU - Bonnotte, Bernard
PY - 2011/9/1
Y1 - 2011/9/1
N2 - Known for years as professional APCs, dendritic cells (DCs) are also endowed with tumoricidal activity. This dual role of DC as killers and messengers may have important implications for tumor immunotherapy. However, the tumoricidal activity of DCs has mainly been investigated in animal models. Cancer cells inhibit antitumor immune responses using numerous mechanisms, including the induction of immunosuppressive/ tolerogenic DCs that have lost their ability to present Ags in an immunogenic manner. In this study, we evaluated the possibility of generating tumor killer DCs from patients with advanced-stage cancers. We demonstrate that human monocyte-derived DCs are endowed with significant cytotoxic activity against tumor cells following activation with LPS. The mechanism of DC-mediated tumor cell killing primarily involves peroxynitrites. This observed cytotoxic activity is restricted to immature DCs. Additionally, after killing, these cytotoxic DCs are able to activate tumor Ag-specific T cells. These observations may open important new perspectives for the use of autologous cytotoxic DCs in cancer immunotherapy strategies.
AB - Known for years as professional APCs, dendritic cells (DCs) are also endowed with tumoricidal activity. This dual role of DC as killers and messengers may have important implications for tumor immunotherapy. However, the tumoricidal activity of DCs has mainly been investigated in animal models. Cancer cells inhibit antitumor immune responses using numerous mechanisms, including the induction of immunosuppressive/ tolerogenic DCs that have lost their ability to present Ags in an immunogenic manner. In this study, we evaluated the possibility of generating tumor killer DCs from patients with advanced-stage cancers. We demonstrate that human monocyte-derived DCs are endowed with significant cytotoxic activity against tumor cells following activation with LPS. The mechanism of DC-mediated tumor cell killing primarily involves peroxynitrites. This observed cytotoxic activity is restricted to immature DCs. Additionally, after killing, these cytotoxic DCs are able to activate tumor Ag-specific T cells. These observations may open important new perspectives for the use of autologous cytotoxic DCs in cancer immunotherapy strategies.
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U2 - 10.4049/jimmunol.1004146
DO - 10.4049/jimmunol.1004146
M3 - Article
C2 - 21804019
AN - SCOPUS:80052655776
SN - 0022-1767
VL - 187
SP - 2775
EP - 2782
JO - Journal of Immunology
JF - Journal of Immunology
IS - 5
ER -