Mamilos Andreas, Lein Alexander, Winter Lina, Ettl Tobias, Künzel Julian, Reichert Torsten E, Spanier Gerrit, Brochhausen Christoph
Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Central Biobank Regensburg, University and University Hospital Regensburg, 93053 Regensburg, Germany.
J Clin Med. 2023 Feb 20;12(4):1704. doi: 10.3390/jcm12041704.
Evaluating the tumor microenvironment and its influence on clinical management and therapy response is becoming increasingly important. However, only a few studies deal with the spatial distribution of immune cells within the tumor. This study aimed to describe the topology of immune cells in the microenvironment of oral squamous cell carcinoma (OSCC) sectioned by tumor invasion front and tumor center and to test their prognostic relevance regarding patient survival.
A total of 55 OSCC patient specimens were collected retrospectively. The cancer tissue was immunohistochemically stained using an automated tissue stainer Ventana Benchmark Ultra (Roche) and analyzed using discrete expression marker profiles on immune cells. We investigated CD4+ lymphocytes, CD8+ lymphocytes, CD68+ macrophages, CD163+ macrophages, and M1 macrophages regarding their spatial distribution.
The statistical analysis revealed that the quantity and distribution of CD4+ ( = 0.007), CD8+ ( < 0.001), CD68+ ( < 0.001), CD163+ cells ( = 0.004), and M1 ( < 0.001) macrophages were significantly higher at the invasion front compared to the tumor center in all observed cases. However, high and low immune cell counts in the tumor center and invasion front were not associated with overall survival.
Our results show two distinct immune microenvironments of the tumor center compared to the invasion front. Future studies are needed to explore how these results can be leveraged to improve patient therapy and outcome.
评估肿瘤微环境及其对临床管理和治疗反应的影响变得越来越重要。然而,只有少数研究涉及肿瘤内免疫细胞的空间分布。本研究旨在描述经肿瘤浸润前沿和肿瘤中心切片的口腔鳞状细胞癌(OSCC)微环境中免疫细胞的拓扑结构,并测试它们与患者生存的预后相关性。
回顾性收集了55例OSCC患者标本。使用自动组织染色仪Ventana Benchmark Ultra(罗氏公司)对癌组织进行免疫组织化学染色,并使用免疫细胞上的离散表达标记谱进行分析。我们研究了CD4+淋巴细胞、CD8+淋巴细胞、CD68+巨噬细胞、CD163+巨噬细胞和M1巨噬细胞的空间分布。
统计分析显示,在所有观察病例中,与肿瘤中心相比,浸润前沿的CD4+(=0.007)、CD8+(<0.001)、CD68+(<0.001)、CD163+细胞(=0.004)和M1(<0.001)巨噬细胞的数量和分布显著更高。然而,肿瘤中心和浸润前沿的免疫细胞高计数和低计数与总生存期无关。
我们的结果显示,与浸润前沿相比,肿瘤中心有两种不同的免疫微环境。未来需要开展研究,以探索如何利用这些结果来改善患者治疗和预后。