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Abstract
Dendritic cells (DCs) are essential in immunity owing to their role in activating
T cells, thereby promoting antitumor responses. Tumor cells, however, hijack the immune
system, causing T cell exhaustion and DC dysfunction. Tumor-induced T cell exhaustion
may be reversed through immune checkpoint blockade (ICB); however, this treatment
fails to show clinical benefit in many patients. While ICB serves to reverse T cell
exhaustion, DCs are still necessary to prime, activate, and direct the T cells to
target tumor cells. In this review we provide a brief overview of DC function, describe
mechanisms by which DC functions are disrupted by the tumor microenvironment, and
highlight recent developments in DC cancer vaccines.