非常规 T 细胞在泌尿系统肿瘤中:能抓住就抓住
Unconventional T cells in urological cancers: catch them if you can.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The prognostic and clinicopathological significance of Tim-3 and PD-1 expression in the prognosis of upper urinary tract urothelial carcinoma.
The prognostic and clinicopathological significance of Tim-3 and PD-1 expression in the prognosis of upper urinary tract urothelial carcinoma.
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我们证实,Tim-3 蛋白高表达可作为 UTUC 患者较早发生 IVR 和较短 OS 的指标,而 PD-1 高表达仅与较早发生 IVR 相关。我们发现,Tim-3 在肿瘤复发和进展中的作用比 PD-1 更重要。总体而言,我们的研究结果支持将 Tim-3 和 PD-1 作为提示患者生存不良的临床预后因素。Tim-3 单独或与 PD-1 联合,可能成为未来 UTUC 治疗的靶点,但仍需进一步的前瞻性研究。
上尿路尿路上皮癌(UTUC)是一种相对少见的疾病,报道的分子标志物很少。本研究评估了原发性UTUC中Tim-3和PD-1的表达及其对患者临床结局的影响。
采用免疫组化法检测101例UTUC患者石蜡包埋切片中Tim-3和PD-1蛋白的表达。H-score与临床病理结局及长期复发率和生存率进行相关性分析。
T细胞免疫球蛋白黏蛋白-3(Tim-3)蛋白在UTUC细胞中过表达,尤其是在TIL(肿瘤浸润淋巴细胞)(TILs)和内皮细胞中。我们发现95%(95/101)的UTUC组织存在Tim-3表达失调,其中44%(44/101)显示高表达。Tim-3高表达(H-score≥100)与晚期病理分级、晚期T分期和肿瘤复发显著相关(P=0.016、0.001和<0.001),并与较差的膀胱内无复发生存期(IRFS)和总生存期(OS)相关(P<0.001和0.003)。此外,本研究还评估了另一种免疫检查点分子——程序性死亡受体-1(PD-1)。在Tim-3低表达亚组患者中,PD-1高表达者比PD-1低表达者更常发生膀胱内复发(IVR)(P<0.001)。然而,在Tim-3高表达亚组中,PD-1表达水平对预后无影响。
Upper urinary tract urothelial carcinoma (UTUC) is a relatively uncommon disease with few reported molecular markers. This study evaluated Tim-3 and PD-1 expression in primary UTUC and its impact on patients' clinical outcomes.
Tim-3 and PD-1 protein expression was detected by immunohistochemistry in paraffin-embedded sections from 101 UTUC patients. The H-score was correlated with clinicopathologic outcomes and the long-term recurrence and survival rates.
T cell immunoglobulin mucin-3 (Tim-3) protein was overexpressed in UTUC cells, especially tumour-infiltrating lymphocytes (TILs) and endothelial cells. We found that 95% (95/101) of UTUC tissues had dysregulated Tim-3 expression, of which 44% (44/101) showed high expression. High Tim-3 expression (H-score≥100) was significantly correlated with advanced pathological grade, advanced T stage and tumour recurrence (P=0.016, 0.001 and < 0.001, respectively) and with poor intravesical recurrence-free survival (IRFS) and overall survival (OS) (P< 0.001 and 0.003). Moreover, another immune checkpoint molecule, programmed death receptor-1 (PD-1), was also assessed in our study. Among patients in the low Tim-3 expression subgroup, those with high PD-1 expression experienced intravesical recurrence (IVR) more often than those with low PD-1 expression (P< 0.001). However, the PD-1 expression level had no effect on prognosis in the high Tim-3 expression subgroup.
We confirmed that high Tim-3 protein expression can be used as an indicator of earlier IVR and shorter OS in patients with UTUC, while high expression of PD-1 is only related to earlier IVR. We showed that Tim-3 plays a more important role in tumour recurrence and progression than PD-1. Collectively, our findings support the use of Tim-3 and PD-1 as clinical prognostic factors indicating poor patient survival. Tim-3, alone or in combination with PD-1, could become a target for future UTUC therapies, but further prospective studies are needed.
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