Department of Surgery and Science, Graduate School of Medical Science, Kyushu University, Fukuoka, Japan.
Centre for Integration of Advanced Medicine, Life Science and Innovative Technology, Kyushu University, Fukuoka, Japan.
Histopathology. 2018 Mar;72(4):697-703. doi: 10.1111/his.13400. Epub 2017 Dec 13.
Programmed cell death-ligand 1 (PD-L1) expression is observed in patients with microsatellite instability-high (MSI-H) colon cancer, which is susceptible to immune checkpoint blockade. The aim of this study was to investigate the interrelationship between PD-L1-positive cells and cytotoxic T cells, lymphatic vessels and vascular endothelium by using histological examination with the three-dimensional (3D) reconstruction of a PD-L1-positive colon cancer.
Serial sections of MSI-H colon cancer tissue were stained with haematoxylin and eosin (H&E) and Masson trichrome stains; immunohistochemical analysis of PD-L1, CD8, D2-40 and CD31 was performed. Several 3D models of MSI-H colon cancer were reconstructed with a 3D data visualisation system. Moreover, 18 serial sections were stained with PD-L1, cytokeratin AE1/AE3, CD45, CD31, CD68 and H&E in the same case to confirm that PD-L1 was expressed on tumour cells, CD31-positive cells and macrophages in the invasive frontal region. Notably, there was a peak in the expression of PD-L1 and CD31 in the invasive frontal region. D2-40-positive cells were abundant in the overall tumour stroma, and CD8-positive cells infiltrated the tumour parenchyma. PD-L1 was expressed on tumour cells in the parenchyma and other cells in the stroma. Additional staining of 18 consecutive sections revealed that the other cells were CD68-positive and CD45-positive macrophages and CD31-positive proliferating vascular endothelial cells.
We confirmed that PD-L1 was highly expressed in the invasive frontal region in 3D models of MSI-H colon cancer tissue. This method can be useful for accurately evaluating the localisation of immune checkpoint molecules.
程序性细胞死亡配体 1(PD-L1)在微卫星高度不稳定(MSI-H)结肠癌患者中表达,这使其易受免疫检查点阻断的影响。本研究旨在通过对 MSI-H 结肠癌的 PD-L1 阳性组织进行组织学检查和三维(3D)重建,研究 PD-L1 阳性细胞与细胞毒性 T 细胞、淋巴管和血管内皮之间的相互关系。
对 MSI-H 结肠癌组织进行苏木精和伊红(H&E)及 Masson 三色染色的连续切片;进行 PD-L1、CD8、D2-40 和 CD31 的免疫组织化学分析。使用 3D 数据可视化系统对 MSI-H 结肠癌的多个 3D 模型进行重建。此外,在同一例中对 18 个连续切片用 PD-L1、细胞角蛋白 AE1/AE3、CD45、CD31、CD68 和 H&E 进行染色,以确认 PD-L1 在肿瘤细胞、CD31 阳性细胞和浸润前缘的巨噬细胞上表达。值得注意的是,在浸润前缘 PD-L1 和 CD31 的表达呈峰值。D2-40 阳性细胞在整个肿瘤基质中丰富,CD8 阳性细胞浸润肿瘤实质。PD-L1 在实质中的肿瘤细胞和基质中的其他细胞上表达。对 18 个连续切片的进一步染色显示,其他细胞是 CD68 阳性和 CD45 阳性的巨噬细胞以及 CD31 阳性的增殖性血管内皮细胞。
我们在 MSI-H 结肠癌组织的 3D 模型中证实,PD-L1 在浸润前缘高度表达。这种方法可用于准确评估免疫检查点分子的定位。