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Distribution and characterization of tumor-associated macrophages/microglia in rat C6 glioma

机译:大鼠C6胶质瘤中肿瘤相关巨噬细胞/小胶质细胞的分布和特征

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摘要

Immunity responses and immunotherapy are novel areas of research for the pathological development and treatment of glioma, the most common brain cancer. Characterization of the subpopulations of infiltrated immune cells may aid in our understanding of the tumor immune response and contribute to the identification of cellular targets for selective immunotherapy. Using a rat C6 glioma model, the present study observed a significant heterogeneity of active macrophages and microglia, including cluster of differentiation 8 (CD8)+, endothelial monocyte?activating polypeptide II (EMAPII)+ and ED1+ cells, mostly in the areas of compact tumor growth and inside or around the pannecrosis. Moreover, the CD8+ cells were similar to reactive ED1+ and EMAPII+ microglia/macrophages in morphology and distribution, but different from the W3/13+ T cells. These observations suggest that different subtypes of macrophages and microglia are involved in glioma development and thus, may be potential targets for immunotherapeutic antitumor strategies.
机译:免疫应答和免疫疗法是神经胶质瘤(最常见的脑癌)的病理发展和治疗研究的新领域。浸润免疫细胞亚群的特征可能有助于我们了解肿瘤的免疫反应,并有助于确定选择性免疫疗法的细胞靶标。使用大鼠C6胶质瘤模型,本研究观察到了活性巨噬细胞和小胶质细胞的显着异质性,包括分化簇8(CD8)+,内皮单核细胞活化多肽II(EMAPII)+和ED1 +细胞,主要存在于致密区域肿瘤的生长和坏死的内部或周围。此外,CD8 +细胞在形态和分布上与反应性ED1 +和EMAPII +小胶质细胞/巨噬细胞相似,但与W3 / 13 + T细胞不同。这些观察结果表明,不同的亚型巨噬细胞和小胶质细胞参与神经胶质瘤的发展,因此可能是免疫治疗抗肿瘤策略的潜在目标。

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