Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, 204 Craft Ave, Pittsburgh, PA, 15213, USA.
Cancer Immunol Immunother. 2015 Sep;64(9):1095-108. doi: 10.1007/s00262-015-1712-6. Epub 2015 May 22.
Monoclonal antibodies that block inhibitory immune checkpoint molecules and enhance anti-tumor responses show clinical promise in advanced solid tumors. Most of the preliminary evidence on therapeutic efficacy of immune checkpoint blockers comes from studies in melanoma, lung and renal cancer. To test the in vivo potential of programmed death-ligand 1 (PD-L1) blockade in ovarian cancer, we recently generated a new transplantable tumor model using human mucin 1 (MUC1)-expressing 2F8 cells. The MUC1 transgenic (MUC1.Tg) mice develop large number of intraperitoneal (IP) tumors following IP injection of 8 × 10(5) syngeneic 2F8 cells. The tumors are aggressive and display little T cell infiltration. Anti-PD-L1 antibody was administered IP every 2 weeks (200 μg/dose) for a total of three doses. Treatment was started 21 days post-tumor challenge, a time point which corresponds to late tumor stage. The anti-PD-L1 treatment led to substantial T cell infiltration within the tumor and significantly increased survival (p = 0.001) compared to isotype control-treated mice. When the same therapy was administered to wild-type mice challenged with 2F8 tumors, no survival benefit was observed, despite the presence of high titer anti-MUC1 antibodies. However, earlier treatment (day 11) and higher frequency of IP injections restored the T cell responses and led to prolonged survival. Splenocyte profiling via Nanostring using probes for 511 immune genes revealed a treatment-induced immune gene signature consistent with increased T cell-mediated immunity. These findings strongly support further preclinical and clinical strategies exploring PD-L1 blockade in ovarian cancer.
阻断抑制性免疫检查点分子并增强抗肿瘤反应的单克隆抗体在晚期实体瘤中显示出临床应用前景。免疫检查点抑制剂治疗疗效的大部分初步证据来自黑色素瘤、肺癌和肾癌的研究。为了测试程序性死亡配体 1(PD-L1)阻断在卵巢癌中的体内潜力,我们最近使用表达人黏蛋白 1(MUC1)的 2F8 细胞生成了一种新的可移植肿瘤模型。MUC1 转基因(MUC1.Tg)小鼠在腹腔内(IP)注射 8×10(5)同源 2F8 细胞后,会发展出大量的 IP 肿瘤。这些肿瘤具有侵袭性,且显示出很少的 T 细胞浸润。抗 PD-L1 抗体每 2 周通过 IP 给药(200μg/剂量),共给药 3 次。治疗于肿瘤接种后 21 天开始,这一时间点对应于晚期肿瘤阶段。与同型对照治疗的小鼠相比,抗 PD-L1 治疗导致肿瘤内大量 T 细胞浸润,并显著提高了生存率(p=0.001)。当相同的治疗方案应用于接受 2F8 肿瘤挑战的野生型小鼠时,尽管存在高滴度的抗 MUC1 抗体,但没有观察到生存获益。然而,早期治疗(第 11 天)和更高频率的 IP 注射恢复了 T 细胞反应,并延长了生存时间。通过 Nanostring 使用针对 511 个免疫基因的探针对脾细胞进行分析,揭示了一种治疗诱导的免疫基因特征,与增强的 T 细胞介导的免疫一致。这些发现强烈支持进一步探索 PD-L1 阻断在卵巢癌中的临床前和临床策略。