Department of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 252 50 Vestec, Czech Republic.
Department of Cell Biology, Faculty of Science, Charles University, BIOCEV, 252 50 Vestec, Czech Republic.
Int J Mol Sci. 2020 Mar 6;21(5):1806. doi: 10.3390/ijms21051806.
Programmed cell death protein 1 (PD-1)/PD-1 ligand 1 (PD-L1) blockade is a promising therapy for various cancer types, but most patients are still resistant. Therefore, a larger number of predictive biomarkers is necessary. In this study, we assessed whether a loss-of-function mutation of the interferon (IFN)-γ receptor 1 (IFNGR1) in tumor cells can interfere with anti-PD-L1 therapy. For this purpose, we used the mouse oncogenic TC-1 cell line expressing PD-L1 and major histocompatibility complex class I (MHC-I) molecules and its TC-1/A9 clone with reversibly downregulated PD-L1 and MHC-I expression. Using the CRISPR/Cas9 system, we generated cells with deactivated IFNGR1 (TC-1/dIfngr1 and TC-1/A9/dIfngr1). In tumors, IFNGR1 deactivation did not lead to PD-L1 or MHC-I reduction on tumor cells. From potential inducers, mainly IFN-α and IFN-β enhanced PD-L1 and MHC-I expression on TC-1/dIfngr1 and TC-1/A9/dIfngr1 cells in vitro. Neutralization of the IFN-α/IFN-β receptor confirmed the effect of these cytokines in vivo. Combined immunotherapy with PD-L1 blockade and DNA vaccination showed that IFNGR1 deactivation did not reduce tumor sensitivity to anti-PD-L1. Thus, the impairment of IFN-γ signaling may not be sufficient for PD-L1 and MHC-I reduction on tumor cells and resistance to PD-L1 blockade, and thus should not be used as a single predictive marker for anti-PD-1/PD-L1 cancer therapy.
程序性细胞死亡蛋白 1(PD-1)/PD-1 配体 1(PD-L1)阻断是各种癌症类型的一种有前途的治疗方法,但大多数患者仍然有耐药性。因此,需要更多的预测性生物标志物。在这项研究中,我们评估了肿瘤细胞中干扰素(IFN)-γ受体 1(IFNGR1)的功能丧失突变是否会干扰抗 PD-L1 治疗。为此,我们使用表达 PD-L1 和主要组织相容性复合体 I(MHC-I)分子的小鼠致癌 TC-1 细胞系及其 PD-L1 和 MHC-I 表达可逆下调的 TC-1/A9 克隆。使用 CRISPR/Cas9 系统,我们生成了失活 IFNGR1 的细胞(TC-1/dIfngr1 和 TC-1/A9/dIfngr1)。在肿瘤中,IFNGR1 失活不会导致肿瘤细胞上 PD-L1 或 MHC-I 的减少。从潜在的诱导剂来看,主要是 IFN-α 和 IFN-β 增强了 TC-1/dIfngr1 和 TC-1/A9/dIfngr1 细胞体外的 PD-L1 和 MHC-I 表达。IFN-α/IFN-β 受体的中和证实了这些细胞因子在体内的作用。PD-L1 阻断和 DNA 疫苗联合免疫治疗表明,IFNGR1 失活不会降低肿瘤对抗 PD-L1 的敏感性。因此,IFN-γ 信号的损害可能不足以减少肿瘤细胞上的 PD-L1 和 MHC-I 并对 PD-L1 阻断产生耐药性,因此不应将其用作抗 PD-1/PD-L1 癌症治疗的单一预测标志物。