Department of Immunology and Inflammation, Humanitas Clinical and Research Center-IRCCS, Rozzano, Italy.
Department of Biomedical Science, Humanitas University, Rozzano, Italy.
Cell Mol Immunol. 2021 Mar;18(3):566-578. doi: 10.1038/s41423-020-00613-4. Epub 2021 Jan 20.
Myeloid cells in tumor tissues constitute a dynamic immune population characterized by a non-uniform phenotype and diverse functional activities. Both tumor-associated macrophages (TAMs), which are more abundantly represented, and tumor-associated neutrophils (TANs) are known to sustain tumor cell growth and invasion, support neoangiogenesis and suppress anticancer adaptive immune responses. In recent decades, several therapeutic approaches have been implemented in preclinical cancer models to neutralize the tumor-promoting roles of both TAMs and TANs. Some of the most successful strategies have now reached the clinic and are being investigated in clinical trials. In this review, we provide an overview of the recent literature on the ever-growing complexity of the biology of TAMs and TANs and the development of the most promising approaches to target these populations therapeutically in cancer patients.
肿瘤组织中的髓系细胞构成了一个动态的免疫群体,其特征为非均一的表型和多样化的功能活性。肿瘤相关巨噬细胞(TAMs)和肿瘤相关中性粒细胞(TANs)都与肿瘤细胞的生长和侵袭、支持新生血管生成以及抑制抗肿瘤适应性免疫反应有关,其中 TAMs 更为丰富。在过去的几十年中,已经在临床前癌症模型中实施了几种治疗方法来中和 TAMs 和 TANs 的促肿瘤作用。其中一些最成功的策略现已进入临床,并在临床试验中进行研究。在这篇综述中,我们概述了关于 TAMs 和 TANs 生物学的日益复杂的最新文献,并介绍了针对这些细胞群体进行治疗的最有前途的方法。