Comparative analyses of immune cells and alpha-smooth muscle actin-positive cells under the immunological microenvironment between with and without dense fibrosis in primary central nervous system lymphoma.

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY Brain Tumor Pathology Pub Date : 2024-10-01 Epub Date: 2024-08-26 DOI:10.1007/s10014-024-00488-7
Jun Takei, Miku Maeda, Nei Fukasawa, Masaharu Kawashima, Misayo Miyake, Kyoichi Tomoto, Shohei Nawate, Akihiko Teshigawara, Tomoya Suzuki, Yohei Yamamoto, Hiroyasu Nagashima, Ryosuke Mori, Ryoko Fukushima, Satoshi Matsushima, Hiroyoshi Kino, Ai Muroi, Takao Tsurubuchi, Noriaki Sakamoto, Kaichi Nishiwaki, Shingo Yano, Yuzuru Hasegawa, Yuichi Murayama, Yasuharu Akasaki, Masayuki Shimoda, Eiichi Ishikawa, Toshihide Tanaka
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Abstract

Histopathologic examinations of primary central nervous system lymphoma (PCNSL) reveal concentric accumulation of lymphocytes in the perivascular area with fibrosis. However, the nature of this fibrosis in "stiff" PCNSL remains unclear. We have encountered some PCNSLs with hard masses as surgical findings. This study investigated the dense fibrous status and tumor microenvironment of PCNSLs with or without stiffness. We evaluated by silver-impregnation nine PCNSLs with stiffness and 26 PCNSLs without stiffness. Six of the nine stiff PCNSLs showed pathological features of prominent fibrosis characterized by aggregation of reticulin fibers, and collagen accumulations. Alpha-smooth muscle actin (αSMA)-positive spindle cells as a cancer-associated fibroblast, the populations of T lymphocytes, and macrophages were compared between fibrous and control PCNSLs. Fibrous PCNSLs included abundant αSMA-positive cells in both intra- and extra-tumor environments (5/6, 87% and 3/6, 50%, respectively). Conversely, only one out of the seven control PCNSL contained αSMA-positive cells in the intra-tumoral area. Furthermore, the presence of extra-tumoral αSMA-positive cells was associated with infiltration of T lymphocytes and macrophages. In conclusion, recognizing the presence of dense fibrosis in PCNSL can provide insights into the tumor microenvironment. These results may help stratify patients with PCNSL and improve immunotherapies for these patients.

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原发性中枢神经系统淋巴瘤有致密纤维化和无致密纤维化免疫微环境下免疫细胞和α-平滑肌肌动蛋白阳性细胞的比较分析。
原发性中枢神经系统淋巴瘤(PCNSL)的组织病理学检查显示,淋巴细胞在血管周围同心聚集,并伴有纤维化。然而,"僵硬 "PCNSL 中纤维化的性质仍不清楚。我们曾遇到过一些手术发现有硬块的 PCNSL。本研究调查了有无硬块的 PCNSL 的致密纤维状态和肿瘤微环境。我们通过银浸渍法评估了 9 例有硬块的 PCNSL 和 26 例无硬块的 PCNSL。在 9 个僵硬的 PCNSL 中,有 6 个表现出突出的纤维化病理特征,其特点是网状纤维聚集和胶原堆积。对纤维性 PCNSL 和对照组 PCNSL 的α-平滑肌肌动蛋白(αSMA)阳性纺锤体细胞(癌症相关成纤维细胞)、T 淋巴细胞和巨噬细胞的数量进行了比较。纤维状 PCNSL 在瘤内和瘤外环境中都有大量的 αSMA 阳性细胞(分别为 5/6, 87% 和 3/6, 50% )。相反,7 个对照 PCNSL 中只有 1 个在瘤内区域含有 αSMA 阳性细胞。此外,瘤外 αSMA 阳性细胞的存在与 T 淋巴细胞和巨噬细胞的浸润有关。总之,识别 PCNSL 中致密纤维化的存在有助于深入了解肿瘤微环境。这些结果可能有助于对 PCNSL 患者进行分层,并改善这些患者的免疫疗法。
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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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