Differential PI3K delta Signaling in CD4(+) T-cell Subsets Enables Selective Targeting of T Regulatory Cells to Enhance Cancer Immunotherapy

作者：Ahmad Shamim; Abu Eid Rasha; Shrimali Rajeev; Webb Mason; Verma Vivek; Doroodchi Atbin; Berrong Zuzana; Samara Raed; Rodriguez Paulo C; Mkrtichyan Mikayel; Khleif Samir N^*

来源：Cancer Research, 2017, 77(8): 1892-1904.

DOI：10.1158/0008-5472.CAN-16-1839

To modulate T-cell function for cancer therapy, one challenge is to selectively attenuate regulatory but not conventional CD4(+) T-cell subsets [regulatory T cell (Treg) and conventional T cell (Tconv)]. In this study, we show how a functional dichotomy in Class IA PI3K isoforms in these two subsets of CD4(+) T cells can be exploited to target Treg while leaving Tconv intact. Studies employing isoform-specific PI3K inhibitors and a PI3K delta-deficient mouse strain revealed that PI3K alpha and PI3K beta were functionally redundant with PI3K delta in Tconv. Conversely, PI3K delta was functionally critical in Treg, acting there to control T-cell receptor signaling, cell proliferation, and survival. Notably, in a murine model of lung cancer, coadministration of a PI3K delta-specific inhibitor with a tumor-specific vaccine decreased numbers of suppressive Treg and increased numbers of vaccine-induced CD8 T cells within the tumor microenvironment, eliciting potent antitumor efficacy. Overall, our results offer a mechanistic rationale to employ PI3K delta inhibitors to selectively target Treg and improve cancer immunotherapy.

• 出版日期2017-4-15