4.8 Review

DCision-making in tumors governs T cell anti-tumor immunity

Journal

ONCOGENE
Volume 40, Issue 34, Pages 5253-5261

Publisher

SPRINGERNATURE
DOI: 10.1038/s41388-021-01946-8

Keywords

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Funding

  1. Swiss Government Excellence Fellowship
  2. EMBO Postdoctoral Fellowship
  3. European Research Council [802773-MitoGuide]
  4. SNSF [31003A_182470]
  5. Cancer Research Institute (CLIP investigator award)
  6. Cancer Research Institute (Lloyd J. Old STAR award)
  7. NIH NIAID Career Transition Award [K22AI143960]
  8. Ludwig Cancer Research

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The role of dendritic cells in regulating T cell immune responses is critical, but interactions may be disrupted by the tumor microenvironment. This review discusses how T cell activation is controlled and how the tumor microenvironment alters dendritic cell properties, highlighting therapeutic options for influencing dendritic cell-mediated decisions in T cells for cancer treatment.
The exploitation of T cell-based immunotherapies and immune checkpoint blockade for cancer treatment has dramatically shifted oncological treatment paradigms and broadened the horizons of cancer immunology. Dendritic cells have emerged as the critical tailors of T cell immune responses, which initiate and coordinate anti-tumor immunity. Importantly, genetic alterations in cancer cells, cytokines and chemokines produced by cancer and stromal cells, and the process of tumor microenvironmental regulation can compromise dendritic cell-T cell cross-talk, thereby disrupting anti-tumor T cell responses. This review summarizes how T cell activation is controlled by dendritic cells and how the tumor microenvironment alters dendritic cell properties in the context of the anti-tumor immune cycle. Furthermore, we will highlight therapeutic options for tailoring dendritic cell-mediated decision-making in T cells for cancer treatment.

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