肿瘤微环境
彭布罗利珠单抗
医学
细胞毒性T细胞
癌症研究
CD8型
白细胞介素2受体
卵巢癌
免疫检查点
免疫疗法
免疫学
抗体
免疫系统
癌症
肿瘤科
T细胞
内科学
生物
体外
生物化学
作者
Faraah Bekheet,Melanie Ashland,Rochelle Reyes,Oliver Dorigo,Amer Karam,Christopher T. Chen
出处
期刊:Immunotherapy
[Future Medicine]
日期:2025-09-02
卷期号:17 (13): 921-925
标识
DOI:10.1080/1750743x.2025.2561398
摘要
Although PD-1 checkpoint inhibition has improved outcomes for some cancer types, a substantial proportion of solid tumors still do not respond, in part due to inadequate cytotoxic CD8+ T-cell infiltration and survival within the tumor microenvironment (TME). CD25+ regulatory T-cells (Tregs) are a subset of T-cells that play a key role in suppressing CD8+ T-cell activity. Depletion of Tregs in the TME could thus enhance anti-cancer immune responses. Here, we present the experience of a patient with platinum-resistant ovarian carcinoma who achieved a durable partial response on a phase 1 clinical trial of an anti-CD25 antibody-drug conjugate combined with pembrolizumab. Notably, her tumor response correlated with a reduction in CD25+ Tregs on paired tumor biopsies and further deepened after treatment discontinuation. This case provides early proof-of-concept that Treg depletion combined with PD-1/PD-L1 inhibitors can lead to anti-cancer efficacy in refractory diseases and offers key lessons to guide future development of anti-Treg therapeutics.
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