Abstract
Effector T cells play an important role for killing abnormal cells such as cancer cells. On the other hand, regulatory T (Treg) cells are essential in immunosuppression to control over-activation of immune responses and maintain immune tolerance. These immune cells are guided from the circulation into local tissues, such as the tumor microenvironment (TME), to exert their functions by the chemokine networks. We clarified the mechanisms by which EGFR-mutated non-small cell lung cancers make non-inflamed TME, while promoting Treg infiltration via CCL22 production.
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