| Literature DB >> 28811970 |
Abhishek D Garg1, Monica Vara Perez1, Marco Schaaf1, Patrizia Agostinis1, Laurence Zitvogel2,3,4,5, Guido Kroemer6,7,8,9,10,11,12, Lorenzo Galluzzi6,13,14.
Abstract
Dendritic cell (DC)-based vaccines against cancer have been extensively developed over the past two decades. Typically DC-based cancer immunotherapy entails loading patient-derived DCs with an appropriate source of tumor-associated antigens (TAAs) and efficient DC stimulation through a so-called "maturation cocktail" (typically a combination of pro-inflammatory cytokines and Toll-like receptor agonists), followed by DC reintroduction into patients. DC vaccines have been documented to (re)activate tumor-specific T cells in both preclinical and clinical settings. There is considerable clinical interest in combining DC-based anticancer vaccines with T cell-targeting immunotherapies. This reflects the established capacity of DC-based vaccines to generate a pool of TAA-specific effector T cells and facilitate their infiltration into the tumor bed. In this Trial Watch, we survey the latest trends in the preclinical and clinical development of DC-based anticancer therapeutics. We also highlight how the emergence of immune checkpoint blockers and adoptive T-cell transfer-based approaches has modified the clinical niche for DC-based vaccines within the wide cancer immunotherapy landscape.Entities:
Keywords: Antigen cross-presentation; DAMPs; TLR signaling; immune-checkpoint blockers; plasmacytoid dendritic cells; tumor-infiltrating lymphocytes
Year: 2017 PMID: 28811970 PMCID: PMC5543823 DOI: 10.1080/2162402X.2017.1328341
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110