TIM 3和凝集素9在儿童尤文氏肉瘤诊断时肿瘤标本免疫组化染色中的高表达。

Stephanie J Si, Gerald B Wertheim, David M Barrett
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引用次数: 1

摘要

近年来,免疫系统调节在癌症治疗方面取得了重大进展。特别是,免疫检查点抑制剂和嵌合抗原受体(CAR) t细胞治疗在复发/难治性癌症中显示出显着的临床益处。然而,我们对儿童实体瘤免疫肿瘤学领域的理解仍然有限,这是继续进步的障碍。我们检测了检查点受体PD-1、TIM-3、LAG-3及其相应配体在各种儿科癌症诊断中的免疫组织化学表达,发现TIM-3/Galectin-9在Ewing肉瘤浸润细胞中高表达。检查点受体/配体表达的位置很重要,因为一些染色模式仅在肿瘤边缘可见。最后,外周T细胞功能在不同肿瘤之间存在显著差异,支持肿瘤微环境与整体免疫系统之间的复杂关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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High Expression of TIM 3 and Galectin 9 on Immunohistochemistry Staining of Tumor Specimen at Diagnosis in Pediatric Patients with Ewing Sarcoma.

Significant progress has been made in the advancement of immune system modulation for cancer treatment in recent years. In particular, immune checkpoint inhibitors and chimeric antigen receptor (CAR) T-cell therapy have demonstrated remarkable clinical benefit in relapsed/refractory cancers. However, our understanding of the immuno-oncologic landscape in pediatric solid tumors remains limited and is a barrier to continued progress. We examined the immunohistochemical expression of checkpoint receptors PD-1, TIM-3, LAG-3 and their respective ligands in various pediatric cancers at diagnosis and found high expression of TIM-3/Galectin-9 in the infiltrating cells of Ewing sarcoma. Location of checkpoint receptor/ligand expressions is important, as some staining patterns were only seen along tumor borders. Finally, peripheral T cell function varied significantly among different tumors supporting a complex relationship between the tumor microenvironment and the global immune system.

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