Suppr超能文献

髓源性抑制细胞(MDSCs):目前我们对它们对抗程序性死亡蛋白1(PD-1)/程序性死亡配体1(PD-L1)疗法的作用了解多少?

Myeloid-derived suppressor cells (MDSCs): what do we currently know about the effect they have against anti-PD-1/PD-L1 therapies?

作者信息

Tellez Ronald Sergio Limón, Reynolds Lucia, Piris Miguel A

机构信息

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.

出版信息

Ecancermedicalscience. 2023 Jun 5;17:1556. doi: 10.3332/ecancer.2023.1556. eCollection 2023.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9f6/10310335/4dc48fa348b5/can-17-1556fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验