Abstract
Immune infiltration of tumors is a well-known phenomenon in cancer patients. Nevertheless, the tumor and immune cell coexisting scenario is often accompanied by efficient cancer progression indicating a compromised immune phenotype. As a matter of fact, it is well documented that a wealthy source of immune-suppressive molecular and cellular networks at the tumor site foster faulty T cell responses and ultimately redirect T cell fate and patient outcome. In this chapter, we summarize recent discoveries of the acquired dysfunctions of effector T cells in the tumor microenvironment due to the lack of proper activation networks and underlying enforcers regulating T cell unresponsiveness and their impact in new therapeutic development. Specifically, the advance in the Th17 balance, T cell stemness, and polyfunctionality of T cells which may improve clinic outcome.
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Crespo, J., Kryczek, I., Welling, T., Wei, S., Zou, W. (2015). T Cell Fate in the Tumor Microenvironment. In: Ascierto, P., Stroncek, D., Wang, E. (eds) Developments in T Cell Based Cancer Immunotherapies. Cancer Drug Discovery and Development. Humana Press, Cham. https://doi.org/10.1007/978-3-319-21167-1_3
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