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Consensus nomenclature for CD8<sup>+</sup>T cell phenotypes in cancer

135

Citations

79

References

2015

Year

Abstract

Whereas preclinical investigations and clinical studies have established that CD8<sup>+</sup> T cells can profoundly affect cancer progression, the underlying mechanisms are still elusive. Challenging the prevalent view that the beneficial effect of CD8<sup>+</sup> T cells in cancer is solely attributable to their cytotoxic activity, several reports have indicated that the ability of CD8<sup>+</sup> T cells to promote tumor regression is dependent on their cytokine secretion profile and their ability to self-renew. Evidence has also shown that the tumor microenvironment can disarm CD8<sup>+</sup> T cell immunity, leading to the emergence of dysfunctional CD8<sup>+</sup> T cells. The existence of different types of CD8<sup>+</sup> T cells in cancer calls for a more precise definition of the CD8<sup>+</sup> T cell immune phenotypes in cancer and the abandonment of the generic terms "pro-tumor" and "antitumor." Based on recent studies investigating the functions of CD8<sup>+</sup> T cells in cancer, we here propose some guidelines to precisely define the functional states of CD8<sup>+</sup> T cells in cancer.

References

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