The Wistar Institute, Philadelphia, Pennsylvania.
Cancer Immunol Res. 2017 Jan;5(1):3-8. doi: 10.1158/2326-6066.CIR-16-0297.
Myeloid cells developed evolutionarily as a major mechanism to protect the host. They evolved as a critical barrier against infections and are important contributors to tissue remodeling. However, in cancer, myeloid cells are largely converted to serve a new master-tumor cells. This process is epitomized by myeloid-derived suppressor cells (MDSC). These cells are closely related to neutrophils and monocytes. MDSCs are not present in the steady state of healthy individuals and appear in cancer and in pathologic conditions associated with chronic inflammation or stress. These cells have emerged as an important contributor to tumor progression. Ample evidence supports a key role for MDSCs in immune suppression in cancer, as well as their prominent role in tumor angiogenesis, drug resistance, and promotion of tumor metastases. MDSCs have a fascinating biology and are implicated in limiting the effects of cancer immunotherapy. Therefore, targeting these cells may represent an attractive therapeutic opportunity. Cancer Immunol Res; 5(1); 3-8. ©2016 AACR.
髓系细胞是进化过程中保护宿主的主要机制。它们作为抵御感染的关键屏障,是组织重塑的重要贡献者。然而,在癌症中,髓系细胞在很大程度上被转化为服务于新的主人——肿瘤细胞。这一过程以髓系来源的抑制细胞(MDSC)为代表。这些细胞与中性粒细胞和单核细胞密切相关。在健康个体的稳定状态下,MDSC 不存在,而在癌症和与慢性炎症或应激相关的病理条件下出现。这些细胞已成为肿瘤进展的重要贡献者。大量证据支持 MDSC 在癌症中的免疫抑制中起关键作用,以及它们在肿瘤血管生成、耐药性和促进肿瘤转移中的突出作用。MDSC 具有迷人的生物学特性,并与限制癌症免疫治疗的效果有关。因此,针对这些细胞可能代表一种有吸引力的治疗机会。癌症免疫学研究; 5(1); 3-8. ©2016AACR。