骨髓系衍生抑制细胞的积累诱导Treg扩张并调节肺恶性瘤进展
Yinghua Wan1, Xiangdong Mu1, Jingquan Zhao1
1Department of Respiratory and Critical Care Medicine, Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, Beijing 102218, P.R. China.
Biomedical reports
|March 27, 2024
概括
骨髓原抑制细胞 (MDSCs) 在肺癌中累积,具有影响T细胞反应的特定子集. 这些表达PD-L1/PD-L2的细胞促进调节性T细胞扩张,可能阻碍抗瘤免疫力.
科学领域:
- 免疫学 免疫学 免疫学
- 在瘤学瘤学.
- 细胞生物学 细胞生物学
背景情况:
- 骨髓原抑制细胞 (MDSCs) 是癌症免疫抑制的关键调节者.
- MDSCs是一组异质的髓状细胞,可以抑制T细胞的反应.
- 了解MDSC子集及其在肺癌中的作用对于开发免疫疗法至关重要.
研究的目的:
- 为了研究T细胞和MDSC子集在肺癌中的作用.
- 分析肺癌患者T细胞和MDSC的表型特征.
- 探索MDSC子集和调控性T细胞 (Tregs) 在肺恶性瘤中的关系.
主要方法:
- 分析了102例肺癌病例和34例健康对照.
- 流细胞测量用于对外围血液中T细胞和MDSC亚组的鉴定和表型表征.
- 试验室共培养试验评估MDSCs对T细胞亡和Treg分化的影响.
主要成果:
- 与健康对照组相比,肺癌患者表现出表达PD-L2和PD-L1的粒细胞样MDSC (G-MDSC) 的频率较低.
- 在肺癌患者中观察到表达PD-L1的单细胞样MDSC (M-MDSC) 的更高频率.
- G-MDSCs和M-MDSCs的频率与PD-1+和CTLA-4+调节性T细胞 (Tregs) 有正相关.
- 在体外,来自肺癌患者的M-MDSC增强了天真T细胞亡并促进了Treg分化.
结论:
- MDSC子集在肺恶性瘤中积累,并有助于免疫抑制.
- 表达PD-L1和PD-L2的MDSC诱导Treg扩张,可能通过PD-1相互作用.
- 这些发现突出了MDSC作为肺癌免疫治疗中的潜在治疗点.
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