Gambichler T, Schröter U, Höxtermann S, Susok L, Stockfleth E, Becker J C
Skin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.
Translational Skin Cancer Research, DKTK Partner Site Essen/Düsseldorf, West German Cancer Center, Dermatology, University Duisburg-Essen, Essen, Germany.
Br J Dermatol. 2020 May;182(5):1214-1220. doi: 10.1111/bjd.18379. Epub 2019 Nov 27.
The role of T regulatory lymphocytes (Tregs) and their immunosuppressive mechanisms in the context of programmed death (PD)-1 blockade is not completely understood.
To assess the impact of PD-1-blocking antibody treatment on Treg subpopulations in the blood.
We studied circulating Treg subpopulations in patients with melanoma under nivolumab or pembrolizumab treatment using flow cytometry and correlated these findings with clinical outcomes.
These analyses revealed that the frequency of CD4 CD25 CD127 PD-1 lymphocytes (PD-1 Tregs) significantly decreased after the first cycle of immunotherapy (23% vs. 8·6%, P = 0·043). Compared with patients who did not show a significant decline of PD-1 Tregs after the first treatment, those who did had better clinical outcomes with respect to progression-free survival (PFS, P = 0·022) and melanoma-specific death (MSD, P = 0·0038). Multivariate analysis confirmed that a significant decline of PD-1 Tregs in peripheral blood after the first treatment cycle is a significant predictor of more favourable PFS and MSD (P = 0·04 and 0·017, respectively). Interestingly, the occurrence of immune-related adverse events was also an independent predictor for decreased risk of MSD (P = 0·047; odds ratio 0·064, 95% confidence interval 0·0042-0·97).
We provide preliminary evidence that circulating PD-1 Tregs rapidly decline after the initiation of treatment with PD-1-blocking antibodies, which is associated with reduced risk of melanoma progression and MSD. Patients showing no decrease of these PD-1 Tregs in peripheral blood are characterized by an impaired response to immune checkpoint blockade and worse outcome. What's already known about this topic? Programmed death (PD)-1-blocking antibodies are highly effective in melanoma treatment. However, more than half of patients do not benefit from this therapy and to date it is difficult to predict which patients will respond to it. What does this study add? PD-1-blocking antibody therapy rapidly results in a decline of circulating PD-1 T regulatory cells (Tregs). What is the translational message? Patients showing a decrease of PD-1 Tregs appear to have better clinical outcome under PD-1 treatment.
在程序性死亡(PD)-1阻断的情况下,调节性T淋巴细胞(Tregs)的作用及其免疫抑制机制尚未完全明确。
评估PD-1阻断抗体治疗对血液中Treg亚群的影响。
我们使用流式细胞术研究了接受纳武单抗或派姆单抗治疗的黑色素瘤患者循环中的Treg亚群,并将这些结果与临床结局相关联。
这些分析显示,免疫治疗的第一个周期后,CD4⁺CD25⁺CD127⁻PD-1淋巴细胞(PD-1 Tregs)的频率显著降低(23%对8.6%,P = 0.043)。与首次治疗后PD-1 Tregs未显著下降的患者相比,那些PD-1 Tregs下降的患者在无进展生存期(PFS,P = 0.022)和黑色素瘤特异性死亡(MSD,P = 0.0038)方面有更好的临床结局。多变量分析证实,首次治疗周期后外周血中PD-1 Tregs的显著下降是更有利的PFS和MSD的显著预测指标(分别为P = 0.04和0.017)。有趣的是,免疫相关不良事件的发生也是MSD风险降低的独立预测指标(P = 0.047;比值比0.064,95%置信区间0.0042 - 0.97)。
我们提供了初步证据,表明在用PD-1阻断抗体治疗开始后,循环中的PD-1 Tregs迅速下降,这与黑色素瘤进展和MSD风险降低相关。外周血中这些PD-1 Tregs未下降的患者表现为对免疫检查点阻断反应受损且结局较差。关于该主题已知的内容有哪些?程序性死亡(PD)-1阻断抗体在黑色素瘤治疗中非常有效。然而,超过一半的患者无法从这种治疗中获益,并且迄今为止很难预测哪些患者会对此有反应。这项研究增加了什么内容?PD-1阻断抗体治疗迅速导致循环中的PD-1调节性T细胞(Tregs)下降。转化信息是什么?在PD-1治疗下,显示PD-1 Tregs下降的患者似乎有更好的临床结局。