TY - JOUR
T1 - Impact of myeloid cells on the efficacy of anticancer chemotherapy
AU - Senovilla, Laura
AU - Aranda, Fernando
AU - Galluzzi, Lorenzo
AU - Kroemer, Guido
N1 - Funding Information:
We are indebted to Dr. Miriam Merad (Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY, US) for her constructive comments on the manuscript and to Dr. Oliver Kepp (Gustave Roussy, Villejuif, France) for assistance with the preparation of figures. Authors are supported by the Ligue contre le Cancer (équipe labelisée); Agence National de la Recherche (ANR) ; Association pour la recherche sur le cancer (ARC) ; Cancéropôle Ile-de-France ; AXA Chair for Longevity Research; Institut National du Cancer (INCa); Fondation Bettencourt-Schueller; Fondation de France; Fondation pour la Recherche Médicale (FRM) ; the European Commission (ArtForce) ; the European Research Council (ERC) ; the LabEx Immuno-Oncology ; the SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE) ; the SIRIC Cancer Research and Personalized Medicine (CARPEM) ; and the Paris Alliance of Cancer Research Institutes (PACRI) .
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Tumors are not immunologically silent but evolve and respond to therapy in the context of a continuous, bi-directional interaction with the host immune system. In line with this notion, several clinically successful chemotherapeutics have been shown to mediate antineoplastic effects as they (re)activate an anticancer immune response that is generally executed by lymphoid cells. Myeloid cells play a central role in this process, not only because they critically regulate the activity of T and B lymphocytes, but also because they exert direct tumoricidal effects, at least in some settings. Here, we discuss the impact of various myeloid cell populations, including macrophages, dendritic cells and myeloid-derived suppressor cells, on the efficacy of anticancer chemotherapy.
AB - Tumors are not immunologically silent but evolve and respond to therapy in the context of a continuous, bi-directional interaction with the host immune system. In line with this notion, several clinically successful chemotherapeutics have been shown to mediate antineoplastic effects as they (re)activate an anticancer immune response that is generally executed by lymphoid cells. Myeloid cells play a central role in this process, not only because they critically regulate the activity of T and B lymphocytes, but also because they exert direct tumoricidal effects, at least in some settings. Here, we discuss the impact of various myeloid cell populations, including macrophages, dendritic cells and myeloid-derived suppressor cells, on the efficacy of anticancer chemotherapy.
UR - http://www.scopus.com/inward/record.url?scp=84902506402&partnerID=8YFLogxK
U2 - 10.1016/j.coi.2014.05.009
DO - 10.1016/j.coi.2014.05.009
M3 - Review article
C2 - 24950501
AN - SCOPUS:84902506402
SN - 0952-7915
VL - 30
SP - 24
EP - 31
JO - Current Opinion in Immunology
JF - Current Opinion in Immunology
IS - 1
ER -