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程序性死亡受体1(PD-1)和淋巴细胞活化基因3(LAG-3)在与 Epstein-Barr 病毒(EBV)相关的儿童霍奇金淋巴瘤中的表达对生存有影响。

PD-1 and LAG-3 expression in EBV-associated pediatric Hodgkin lymphoma has influence on survival.

作者信息

Jimenez Oscar, Mangiaterra Tamara, Colli Sandra, García Lombardi Mercedes, Preciado Maria Victoria, De Matteo Elena, Chabay Paola

机构信息

Multidisciplinary Institute for Investigation in Pediatric Pathologies (IMIPP), CONICET-GCBA, Molecular Biology Laboratory, Pathology Division, Ricardo Gutiérrez Children's Hospital, Buenos Aires, Argentina.

Pathology Division, Ricardo Gutiérrez Children's Hospital, Buenos Aires, Argentina.

出版信息

Front Oncol. 2022 Aug 5;12:957208. doi: 10.3389/fonc.2022.957208. eCollection 2022.

Abstract

In pediatric Hodgkin lymphoma (HL), the inability of the cytotoxic microenvironment induced by EBV presence to eliminate tumor cells could reflect the fact that the virus might be able to induce the expression of exhaustion markers to evade an immune response. Therefore, the expression of exhaustion markers in pediatric EBV-associated HL was evaluated. A balance between cytotoxic GrB and Th1 Tbet markers with regulatory Foxp3 was proved in EBV+ cases. In addition, exclusively in EBV-associated cHL, a correlation between PD-1 and LAG-3 expression was observed. Furthermore, those cases also displayed a trend to worse survival when they expressed LAG-3 and inferior event-free survival when both PD-1 and LAG-3 molecules were present. Therefore, even though a cytotoxic and inflammatory environment was supposed to be triggered by EBV presence in pediatric cHL, it seems that the virus may also induce the synergic effect of inhibitory molecules LAG-3 and PD-1 in this series. These observations may reflect the fact that the permissive and exhausted immune microenvironment succeeds to induce lymphomagenesis.

摘要

在儿童霍奇金淋巴瘤(HL)中,EBV的存在所诱导的细胞毒性微环境无法清除肿瘤细胞,这可能反映出该病毒或许能够诱导耗竭标志物的表达以逃避免疫反应。因此,对儿童EBV相关HL中耗竭标志物的表达进行了评估。在EBV阳性病例中,证实了细胞毒性颗粒酶B(GrB)和Th1转录因子T-bet标志物与调节性叉头框蛋白3(Foxp3)之间的平衡。此外,仅在EBV相关的经典型HL中,观察到程序性死亡受体1(PD-1)与淋巴细胞活化基因3(LAG-3)表达之间存在相关性。此外,当这些病例表达LAG-3时,还表现出预后较差的趋势;当同时存在PD-1和LAG-3分子时,无事件生存期较差。因此,尽管在儿童经典型HL中,EBV的存在理应引发细胞毒性和炎性环境,但在该系列研究中,病毒似乎也能诱导抑制性分子LAG-3和PD-1的协同效应。这些观察结果可能反映出以下事实:宽松且耗竭的免疫微环境成功诱导了淋巴瘤的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e5c/9390066/ab4d95fd6c9f/fonc-12-957208-g001.jpg

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