易普利姆玛
前列腺癌
无容量
医学
免疫疗法
免疫检查点
免疫系统
前列腺
肿瘤微环境
CTLA-4号机组
肿瘤科
癌症
内科学
癌症研究
免疫学
T细胞
作者
Jianjun Gao,John F. Ward,Curtis A. Pettaway,Lewis Z. Shi,Sumit K. Subudhi,Luis M. Vence,Hao Zhao,Jianfeng Chen,Hong Chen,Eleni Efstathiou,Patricia Troncoso,James P. Allison,Christopher J. Logothetis,Ignacio I. Wistuba,Manuel A. Sepúlveda,Jingjing Sun,Jennifer A. Wargo,Jorge Blando,Padmanee Sharma
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2017-03-27
卷期号:23 (5): 551-555
被引量:587
摘要
Prostate cancer is refractory to anti-CTLA-4 therapy, but the reason why is unclear. Padmanee Sharma and colleagues report that the inhibitory molecule VISTA, which negatively regulates T cells, is upregulated on macrophages in prostate tumors that have been treated with anti-CTLA-4 and may play a role in resistance to this immunotherapy. To date, anti-CTLA-4 (ipilimumab) or anti-PD-1 (nivolumab) monotherapy has not been demonstrated to be of substantial clinical benefit in patients with prostate cancer. To identify additional immune-inhibitory pathways in the prostate-tumor microenvironment, we evaluated untreated and ipilimumab-treated tumors from patients in a presurgical clinical trial. Levels of the PD-L1 and VISTA inhibitory molecules increased on independent subsets of macrophages in treated tumors. Our data suggest that VISTA represents another compensatory inhibitory pathway in prostate tumors after ipilimumab therapy.
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