Institute for Advanced Biosciences, Université Grenoble-Alpes, Saint-Martin-d'Hères, France.
Research Center Inserm U1209-CNRS 5309/UGA, Grenoble, France.
Clin Transl Gastroenterol. 2019 Jul;10(7):e00058. doi: 10.14309/ctg.0000000000000058.
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related death worldwide. Today, a promising treatment strategy is focused on the enhancement of antitumor immune responses by immune checkpoint modification. However, as only 20% of patients with HCC are responders, identification of predictive factors is urgently required. Therefore, for the first time, the features of the intrahepatic and circulating immune system in patients with advanced-stage HCC, before and during the treatment, were analyzed.
We collected fresh HCC biopsies, along with adjacent tumor-free liver tissues and peripheral blood samples, from 21 patients with advanced HCC. Furthermore, we performed an extensive immunomonitoring of patients with HCC treated with sorafenib or programmed death (PD)-1/PD-L1 pathway blockade using multiparametric flow cytometry.
We observed that regardless of the treatment, low baseline intratumoral CD4/CD8 T-cell ratio was associated with better overall survival (P = 0.0002). The baseline frequency of intratumoral PD-1 CD8 T cells was significantly lower in patients responding to sorafenib treatment than in the nonresponders (P = 0.0117), and the frequency of circulating PD-1 T cells increased with tumor progression (P = 0.0329). By contrast, responders to PD-1/PD-L1 pathway blockade showed a trend of high baseline frequency of intratumoral PD-1 CD8 T cells. Moreover, we observed a trend of LAG3 and TIM3 upregulation on circulating T cells in nonresponding patients to PD-1/PD-L1 pathway blockade.
Immunosuppressive state, characterized by an enhanced intratumoral CD4/CD8 T-cell ratio, was associated with poor prognosis. Additionally, our results suggest that the frequency of intratumoral PD-1 CD8 T cells may serve as a biomarker to identify which individuals will benefit from which treatment and support the use of combination strategies.
肝细胞癌(HCC)是全球癌症相关死亡的主要原因之一。如今,一种有前途的治疗策略侧重于通过免疫检查点修饰增强抗肿瘤免疫反应。然而,由于只有 20%的 HCC 患者是应答者,因此迫切需要确定预测因素。因此,我们首次分析了晚期 HCC 患者在治疗前后的肝内和循环免疫系统的特征。
我们收集了 21 名晚期 HCC 患者的新鲜 HCC 活检组织以及相邻的无肿瘤肝脏组织和外周血样本。此外,我们使用多参数流式细胞术对接受索拉非尼或程序性死亡(PD)-1/PD-L1 通路阻断治疗的 HCC 患者进行了广泛的免疫监测。
我们发现,无论治疗如何,低基线肿瘤内 CD4/CD8 T 细胞比值与总生存期更好相关(P = 0.0002)。对索拉非尼治疗有反应的患者肿瘤内 PD-1 CD8 T 细胞的基线频率明显低于无反应者(P = 0.0117),而循环 PD-1 T 细胞的频率随着肿瘤进展而增加(P = 0.0329)。相比之下,PD-1/PD-L1 通路阻断治疗的应答者显示出肿瘤内 PD-1 CD8 T 细胞基线频率较高的趋势。此外,我们观察到非应答者的循环 T 细胞中 LAG3 和 TIM3 上调的趋势。
以肿瘤内 CD4/CD8 T 细胞比值增强为特征的免疫抑制状态与预后不良相关。此外,我们的结果表明,肿瘤内 PD-1 CD8 T 细胞的频率可能作为识别哪些个体将从哪种治疗中获益的生物标志物,并支持联合策略的使用。