Guo Yawei, Hong Wenming, Zhang Pengying, Han Dafei, Fang Yilong, Tu Jiajie, Wei Wei
Key Laboratory of Anti-Inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Center of Anti-Inflammatory and Immune Medicine, Institute of Clinical Pharmacology, Anhui Medical University, Hefei, Anhui 230032, P.R. China.
Department of Neurosurgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230032, P.R. China.
Oncol Lett. 2020 Jul;20(1):947-954. doi: 10.3892/ol.2020.11602. Epub 2020 May 13.
Glioma is a type of malignant tumor arising from glial cells of the brain or the spine. Circulation-derived macrophage infiltration is a characteristic of the glioma microenvironment. The polarization status of circulation-derived macrophages in patients with glioma remains unclear. Therefore, the present study aimed to evaluate the polarization status of circulation-derived macrophages in patients with glioma. A total of 40 patients with glioma and 38 healthy volunteers were recruited. The polarization status of macrophage-like cells in the peripheral blood of patients with glioma was evaluated. In addition, the associations between the polarization status of macrophage-like cells and glioma stage or the expression levels of the glioma tumor marker chitinase-3-like protein 1 (also termed YKL-40) were evaluated. The number of macrophage-like cells (CD115CD1cCD2CD15CD19CD14CD16CD11b) was higher in the peripheral blood of patients with glioma compared with that of healthy volunteers. There were fewer M1 macrophage-like cells, and more M2 macrophage-like cells were induced in the peripheral blood of patients with glioma compared with healthy controls. Specifically, the number of M2a/M2b macrophage-like cells increased, whereas that of M2c macrophage-like cells decreased in the peripheral blood of patients with glioma compared with healthy controls. The polarization status of macrophage-like cells in patients with glioma was not significantly associated with glioma stage or with the glioma marker YKL-40. Overall, the results of the present study revealed that the polarization status of macrophage-like cells in the peripheral blood of patients with glioma was abnormal, offering potential novel diagnostic and therapeutic targets, such as different macrophage subsets, for glioma.
胶质瘤是一种起源于脑或脊髓神经胶质细胞的恶性肿瘤。循环来源的巨噬细胞浸润是胶质瘤微环境的一个特征。胶质瘤患者循环来源巨噬细胞的极化状态仍不清楚。因此,本研究旨在评估胶质瘤患者循环来源巨噬细胞的极化状态。共招募了40例胶质瘤患者和38名健康志愿者。评估了胶质瘤患者外周血中巨噬细胞样细胞的极化状态。此外,还评估了巨噬细胞样细胞极化状态与胶质瘤分期或胶质瘤肿瘤标志物几丁质酶-3-样蛋白1(也称为YKL-40)表达水平之间的关联。与健康志愿者相比,胶质瘤患者外周血中巨噬细胞样细胞(CD115⁺CD1c⁺CD2⁻CD15⁻CD19⁻CD14⁺CD16⁺CD11b⁺)的数量更高。与健康对照相比,胶质瘤患者外周血中诱导产生的M1巨噬细胞样细胞较少,而M2巨噬细胞样细胞较多。具体而言,与健康对照相比,胶质瘤患者外周血中M2a/M2b巨噬细胞样细胞的数量增加,而M2c巨噬细胞样细胞的数量减少。胶质瘤患者巨噬细胞样细胞的极化状态与胶质瘤分期或胶质瘤标志物YKL-40无显著相关性。总体而言,本研究结果表明,胶质瘤患者外周血中巨噬细胞样细胞的极化状态异常,为胶质瘤提供了潜在的新型诊断和治疗靶点,如不同的巨噬细胞亚群。