促炎细胞因子
趋化因子
免疫学
先天免疫系统
癌症研究
肿瘤微环境
巨噬细胞极化
癌症
细胞毒性T细胞
免疫系统
肿瘤进展
巨噬细胞
生物
医学
炎症
体外
遗传学
生物化学
作者
Paulina Pathria,Tiani L. Louis,Judith A. Varner
标识
DOI:10.1016/j.it.2019.02.003
摘要
Macrophages are phagocytes that serve as a first line of defense against pathogenic insults to tissues. These innate immune cells mount proinflammatory responses to pathogens and repair damaged tissues. However, tumor-associated macrophages (TAMs) express cytokines and chemokines that can suppress antitumor immunity and promote tumor progression. Preclinical studies have identified crucial pathways regulating the recruitment, polarization, and metabolism of TAMs during tumor progression. Moreover, novel therapeutics targeting these pathways can indirectly stimulate cytotoxic T cell activation and recruitment, and synergize with checkpoint inhibitors, chemotherapy and/or radiation therapy in preclinical studies. Thus, clinical trials with therapeutic agents that promote phagocytosis or suppress survival, proliferation, trafficking, or polarization of TAMs are currently underway. These early results offer the promise of improved cancer outcomes.
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