Institute of Clinical Sciences, College of Medical and Dental Sciences, University of Birmingham, Vincent Drive, Edgbaston, Birmingham, B15 2TT, UK.
Celentyx Ltd, Birmingham Research Park, Vincent Drive, Edgbaston, Birmingham, B15 2SQ, UK.
Sci Rep. 2021 Feb 17;11(1):4030. doi: 10.1038/s41598-021-83612-3.
Blockade of PD-1/PD-L1 interactions is proving an exciting, durable therapeutic modality in a range of cancers whereby T cells are released from checkpoint inhibition to revive their inherent anti-tumour activity. Here we have studied various ways to model ex vivo T cell function in order to compare the impact of the clinically utilised anti-PD-1 antibody, pembrolizumab (Keytruda) on the activation of human T cells: focussing on the release of pro-inflammatory IFNγ and anti-inflammatory IL-10 to assess functionality. Firstly, we investigated the actions of pembrolizumab in an acute model of T-cell activation with either immature or mature allogeneic dendritic cells (DCs); pembrolizumab enhanced IFNγ and IL-10 release from purified CD4+ T-cells in the majority of donors with a bias towards pro-inflammatory cytokine release. Next, we modelled the impact of pembrolizumab in settings of more chronic T-cell activation. In a 7-day antigen-specific response to EBV peptides, the presence of pembrolizumab resulted in a relatively modest increase in both IFNγ and IL-10 release. Where pembrolizumab was assessed against long-term stimulated CD4+ cells that had up-regulated the exhaustion markers TIM-3 and PD-1, there was a highly effective enhancement of the otherwise exhausted response to allogeneic DCs with respect to IFNγ production. By contrast, the restoration of IL-10 production was considerably more limited. Finally, to assess a direct clinical relevance we investigated the consequence of PD-1/PD-L1 blockade in the disease setting of dissociated cells from lung and colon carcinomas responding to allogeneic DCs: here, pembrolizumab once more enhanced IFNγ production from the majority of tumour preparations whereas, again, the increase in IL-10 release was modest at best. In conclusion, we have shown that the contribution of PD-1-revealed by using a canonical blocking antibody to interrupt its interaction with PD-L1-to the production of an exemplar pro- and anti-inflammatory cytokine, respectively, depends in magnitude and ratio on the particular stimulation setting and activation status of the target T cell. We have identified a number of in vitro assays with response profiles that mimic features of dissociated cell populations from primary tumours thereby indicating these represent disease-relevant functional assays for the screening of immune checkpoint inhibitors in current and future development. Such in vitro assays may also support patient stratification of those likely to respond to immuno-oncology therapies in the wider population.
阻断 PD-1/PD-L1 相互作用正在证明是一种令人兴奋的、持久的治疗模式,在一系列癌症中,T 细胞从检查点抑制中释放出来,恢复其固有的抗肿瘤活性。在这里,我们研究了各种体外 T 细胞功能的建模方法,以便比较临床上使用的抗 PD-1 抗体 pembrolizumab(Keytruda)对人 T 细胞激活的影响:重点是释放促炎 IFNγ 和抗炎 IL-10 来评估功能。首先,我们研究了 pembrolizumab 在急性 T 细胞激活模型中的作用,使用未成熟或成熟的同种异体树突状细胞 (DC);pembrolizumab 增强了大多数供体中纯化的 CD4+T 细胞的 IFNγ 和 IL-10 释放,偏向于促炎细胞因子释放。接下来,我们模拟了 pembrolizumab 在更慢性 T 细胞激活环境中的影响。在针对 EBV 肽的 7 天抗原特异性反应中,pembrolizumab 的存在导致 IFNγ 和 IL-10 释放相对适度增加。在评估针对已上调耗竭标志物 TIM-3 和 PD-1 的长期刺激的 CD4+细胞的 pembrolizumab 时,对于 IFNγ 产生,对同种异体 DC 的耗竭反应具有高度有效的增强作用。相比之下,IL-10 产生的恢复则要有限得多。最后,为了评估直接的临床相关性,我们研究了 PD-1/PD-L1 阻断在对同种异体 DC 反应的来自肺癌和结肠癌的分离细胞的疾病环境中的后果:在这里,pembrolizumab 再次增强了来自大多数肿瘤制剂的 IFNγ 产生,而 IL-10 释放的增加充其量也只是适度的。总之,我们已经表明,使用经典的阻断抗体来阻断 PD-1 与其 PD-L1 相互作用对分别产生代表性的促炎和抗炎细胞因子的贡献,取决于靶 T 细胞的特定刺激环境和激活状态的大小和比例。我们已经确定了一些具有模拟来自原发性肿瘤的分离细胞群体特征的体外测定方法,从而表明这些方法代表了当前和未来开发中免疫检查点抑制剂筛选的疾病相关功能测定。此类体外测定方法还可以支持对更广泛人群中对免疫肿瘤疗法有反应的患者进行分层。