Tellez Ronald Sergio Limón, Reynolds Lucia, Piris Miguel A
Department of Oncology, University Social Security USS, Nº58 Colon Street, 10260 Santa Cruz, Bolivia.
Associate Medical Oncology and Research, OncoBolivia Specialized Center for Cancer Treatment, Nº236 Azucenas Street, Equipetrol, Santa Cruz, Bolivia.
Ecancermedicalscience. 2023 Jun 5;17:1556. doi: 10.3332/ecancer.2023.1556. eCollection 2023.
Recent advances in cancer treatment such as PD-1/PD-L1 checkpoint inhibitors have prompted multiple research studies to determine all of the factors that influence response or failure to these new treatments. One of those identified factors is myeloid-derived suppressor cells (MDSCs). These cells were identified and described for the first time in 2007 in laboratory mice and cancer patients. Previous studies showed that a greater number of MDSCs was directly related to a greater tumour volume. There are two clearly identified subpopulations: Mononuclear-type myeloid-derived suppressor cells (M-MDSCs) and polymorphonuclear (PMN-MDSCs). These cell population subtypes play a very important role, depending on the type of cancer, since they have the particularity of expressing PD-L1, which interacts with PD-1, inhibiting the expansion of cytotoxic T lymphocytes, promoting resistance to these treatments.
癌症治疗的最新进展,如PD-1/PD-L1检查点抑制剂,促使多项研究去确定所有影响这些新疗法疗效或失效的因素。其中一个已确定的因素是髓源性抑制细胞(MDSCs)。这些细胞于2007年在实验室小鼠和癌症患者中首次被识别和描述。先前的研究表明,MDSCs数量越多,肿瘤体积越大。有两种明确识别出的亚群:单核型髓源性抑制细胞(M-MDSCs)和多形核(PMN-MDSCs)。这些细胞群体亚型发挥着非常重要的作用,这取决于癌症的类型,因为它们具有表达PD-L1的特殊性,PD-L1与PD-1相互作用,抑制细胞毒性T淋巴细胞的扩增,从而促进对这些治疗的抗性。