Abramson Cancer Center; Department of Medicine; Division of Hematology-Oncology; University of Pennsylvania Perelman School of Medicine; Philadelphia, PA USA.
Oncoimmunology. 2013 Dec 1;2(12):e26860. doi: 10.4161/onci.26860. Epub 2013 Nov 4.
Macrophages constitute a dominant fraction of the population of immune cells that infiltrate developing tumors. Recruited by tumor-derived signals, tumor-infiltrating macrophages are key orchestrators of a microenvironment that supports tumor progression. However, the phenotype of macrophages is pliable and, if instructed properly, macrophages can mediate robust antitumor functions through their ability to eliminate malignant cells, inhibit angiogenesis, and deplete fibrosis. While much effort has focused on strategies to block the tumor-supporting activity of macrophages, emerging approaches designed to instruct macrophages with antitumor properties are demonstrating promise and may offer a novel strategy for cancer immunotherapy.
巨噬细胞构成了浸润在发育中的肿瘤中的免疫细胞群体的主要部分。肿瘤衍生的信号招募肿瘤浸润巨噬细胞,它们是支持肿瘤进展的微环境的关键协调者。然而,巨噬细胞的表型是可塑的,如果得到适当的指导,巨噬细胞可以通过消除恶性细胞、抑制血管生成和消耗纤维化来发挥强大的抗肿瘤功能。虽然已经有很多努力集中在阻止巨噬细胞的肿瘤支持活性的策略上,但旨在用抗肿瘤特性指导巨噬细胞的新兴方法正在显示出希望,并可能为癌症免疫治疗提供一种新策略。