Elimination of CD4lowHLA-G+ T cells overcomes castration-resistance in prostate cancer therapy. Issue 11 (November 2018)

• Record Type: Journal Article
• Authors: Wang, Chao; Chen, Jiahuan; Zhang, Qianfei; Li, Wang; Zhang, Shengbo; Xu, Yanjie; Wang, Fang; Zhang, Bing; Zhang, Yan; Gao, Wei-Qiang
• Is Part Of: Cell research. Volume 28:Issue 11(2018)
• Page Start: 1103
• Page End: 1117
• Publication Date: 2018-11
• Subjects: Cells -- Periodicals; Cytology -- Periodicals; Molecular biology -- Periodicals; 571.6
• DOI: 10.1038/s41422-018-0089-4
• Languages: English
• ISSNs: 1001-0602

Abstract

Abstract Androgen deprivation therapy (ADT) is a main treatment for prostate cancer (PCa) but the disease often recurs and becomes castration-resistant in nearly all patients. Recent data implicate the involvement of immune cells in the development of this castration-resistant prostate cancer (CRPC). In particular, T cells have been found to be expanded in both PCa patients and mouse models shortly after androgen deprivation. However, whether or which of the T cell subtypes play an important role during the development of CRPC is unknown. Here we identified a novel population of CD4low HLA-G+ T cells that undergo significant expansion in PCa patients after ADT. In mouse PCa models, a similar CD4low T cell population expands during the early stages of CRPC onset. These cells are identified as IL-4-expressing TH 17 cells, and are shown to be associated with CRPC onset in patients and essential for the development of CRPC in mouse models. Mechanistically, CD4low HLA-G+ T cells drive androgen-independent growth of prostate cancer cells by modulating the activity and migration of CD11blow F4/80hi macrophages. Furthermore, following androgen deprivation, elevated PGE2 -EP2 signaling inhibited the expression of CD4 in thymocytes, and subsequently induced the polarization of CD4low naïve T cells towards the IL-4-expressing TH 17 phenotype via up-regulation of IL23R. Therapeutically, inactivating PGE2 signaling with celecoxib at a time when CD4low HLA-G+ T cells appeared, but not immediately following androgen deprivation, dramatically suppressed the onset of CRPC. Collectively, our results indicate that an unusual population of CD4low HLA-G+ T cells is essential for the development of CRPC and point to a new therapeutic avenue of combining ADT with PGE2 inhibition for the treatment of prostate cancer.