Cellular and Molecular Pathology Laboratory, Faculty of Medicine and Pharmacy, Hassan II University, Casablanca, Morocco.
Department of Neurosurgery, UHC Ibn Rochd, Casablanca, Morocco.
Sci Rep. 2021 Nov 2;11(1):21504. doi: 10.1038/s41598-021-00835-0.
In human gliomas, anti-tumor T cell responses are inhibited through induction of local and systemic immunosuppression. Immune checkpoint blockade is proving to be a success in several types of cancers. However, many studies reported that the treatment of glioblastoma patients with anti-CTLA-4 or anti-PD-1 has no survival benefit compared to standard chemotherapy. This study aimed to investigate the expression and role of VISTA, a newly described immune checkpoint regulator, in human gliomas. mRNA expression was assessed in a total of 87 samples from glioma patients. 57 glioma tissues were taken at different grades. 20 peripheral blood mononuclear cells (PBMC) samples were taken before surgery and ten after surgery, all from the same set of patients. As for the control, ten specimens of PBMC were taken from healthy donors. Protein expression using immunohistochemistry was performed for 30 patients. The Cancer Genome Atlas (TCGA) data set, was also used to investigate VISTA expression through analysis of RNA-seq data of 667 glioma patients. In the Moroccan cohort, VISTA gene expression was significantly upregulated in glioma tissues related to PBMC of healthy donors. This high expression was specific to patient tissues since VISTA expression in PBMC was low when assessed either before or after surgery. Besides, VISTA exhibited higher expression levels in grade III/IV relative to grade I/II glioma patients. Interestingly, VISTA correlated positively with PD-1 expression. PD-1 also showed elevated expressions in higher glioma grades. The TCGA cohort corroborated these observations. Indeed, VISTA was also found to be strongly expressed in high grades. It was positively correlated with other critical immune checkpoints. Finally, increased VISTA transcript levels were associated with weak overall survival of glioma patients. Our study highlighted a correlation between high levels of VISTA expression and poor prognosis in glioma patients. VISTA might be involved in glioma progression and could be considered as a possible new therapeutic target, especially in advanced gliomas.
在人类脑胶质瘤中,通过诱导局部和全身免疫抑制来抑制抗肿瘤 T 细胞反应。免疫检查点阻断在几种类型的癌症中已被证明是成功的。然而,许多研究报告称,与标准化疗相比,用抗 CTLA-4 或抗 PD-1 治疗胶质母细胞瘤患者没有生存获益。本研究旨在研究一种新描述的免疫检查点调节剂 VISTA 在人类脑胶质瘤中的表达和作用。评估了总共 87 名脑胶质瘤患者样本的 mRNA 表达。57 份脑胶质瘤组织取自不同分级。20 份外周血单核细胞 (PBMC) 样本在术前和术后各取 10 份,均取自同一组患者。作为对照,从 10 名健康供者的 PBMC 中取 10 份标本。对 30 名患者进行了免疫组织化学法蛋白表达检测。还通过分析 667 名脑胶质瘤患者的 RNA-seq 数据,使用癌症基因组图谱 (TCGA) 数据集来研究 VISTA 的表达。在摩洛哥队列中,与健康供者 PBMC 相比,VISTA 基因在脑胶质瘤组织中表达显著上调。这种高表达是患者组织特有的,因为术前或术后评估时 PBMC 中的 VISTA 表达较低。此外,VISTA 在 III/IV 级相对于 I/II 级脑胶质瘤患者中表达水平更高。有趣的是,VISTA 与 PD-1 表达呈正相关。PD-1 在较高的脑胶质瘤分级中也表现出较高的表达。TCGA 队列证实了这些观察结果。事实上,VISTA 在高分级中也被发现表达强烈。它与其他关键免疫检查点呈正相关。最后,VISTA 转录水平升高与脑胶质瘤患者总体生存时间较短相关。我们的研究强调了 VISTA 表达水平与脑胶质瘤患者预后不良之间的相关性。VISTA 可能参与脑胶质瘤的进展,可被视为一种可能的新治疗靶点,尤其是在晚期脑胶质瘤中。