Department of Pediatrics, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Department of Pathology, Montefiore Medical Center, Bronx, NY, USA.
Leuk Lymphoma. 2021 Mar;62(3):606-613. doi: 10.1080/10428194.2020.1839651. Epub 2020 Oct 28.
LAG-3, through interaction with a variety of ligands, regulates T cell function inhibition of T cell proliferation and activation. It has been demonstrated to be overexpressed on tumor infiltrating lymphocytes (TILs) of a variety of cancers with associated poor outcomes. The purpose of this study is to characterize the expression pattern and clinical significance of LAG-3 in pediatric Hodgkin lymphoma (HL). Patient tumor samples from Children's Oncology Group clinical trial AHOD0031 with matched patient outcome data were analyzed for the expression of LAG-3 and PD-L1 using immunohistochemistry. 73/115 patients (63%) demonstrated positive LAG-3 staining. No demographic or survival outcome data were significantly associated with LAG-3 expression. Interestingly, patients with the lowest density of expression were found to have the worst EFS, and those with highest density of expression demonstrated the best EFS. There was a positive statistically significant relationship between presence of LAG-3 and PD-L1 expression. This project is innovative in its characterization of LAG-3 as an immune checkpoint target in pediatric HL.
LAG-3 通过与多种配体相互作用,调节 T 细胞功能,抑制 T 细胞增殖和激活。研究表明,LAG-3 在多种癌症的肿瘤浸润淋巴细胞(TILs)中过度表达,与不良预后相关。本研究旨在分析 LAG-3 在儿童霍奇金淋巴瘤(HL)中的表达模式及其临床意义。对儿童肿瘤组临床试验 AHOD0031 的患者肿瘤样本进行分析,采用免疫组织化学法检测 LAG-3 和 PD-L1 的表达。115 例患者中有 73 例(63%)呈 LAG-3 阳性染色。LAG-3 表达与患者的人口统计学或生存结局数据无显著相关性。有趣的是,表达密度最低的患者无事件生存率最差,表达密度最高的患者无事件生存率最好。LAG-3 与 PD-L1 表达之间存在正相关关系。本项目创新性地将 LAG-3 作为儿童 HL 的免疫检查点靶点进行了描述。