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- W166466901 endingPage "518" @default.
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- W166466901 abstract "Dendritic cells (DC) are professional antigen-presenting cells uniquely suited for cancer immunotherapy. They induce primary immune responses, potentiate the effector functions of previously primed T-lymphocytes, and orchestrate communication between innate and adaptive immunity. The remarkable diversity of cytokine activation regimens, DC maturation states, and antigen-loading strategies employed in current DC-based vaccine design reflect an evolving, but incomplete, understanding of optimal DC immunobiology. In the clinical realm, existing DC-based cancer immunotherapy efforts have yielded encouraging but inconsistent results. Despite recent U.S. Federal and Drug Administration (FDA) approval of DC-based sipuleucel-T for metastatic castration-resistant prostate cancer, clinically effective DC immunotherapy as monotherapy for a majority of tumors remains a distant goal. Recent work has identified strategies that may allow for more potent next-generation DC vaccines. Additionally, multimodality approaches incorporating DC-based immunotherapy may improve clinical outcomes." @default.
- W166466901 created "2016-06-24" @default.
- W166466901 creator A5001060160 @default.
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- W166466901 creator A5052836619 @default.
- W166466901 creator A5063075685 @default.
- W166466901 creator A5083708368 @default.
- W166466901 date "2014-12-01" @default.
- W166466901 modified "2023-09-26" @default.
- W166466901 title "Optimizing dendritic cell-based approaches for cancer immunotherapy." @default.
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