可溶性单体人类编程细胞死亡配体1抑制激活的T细胞的功能
Zhaoduan Liang1,2, Wenfang Chen2, Yunzhuo Guo2,3
1Bioland Laboratory, Guangzhou Regenerative Medicine and Health GuangDong Laboratory, Guangzhou, Guangdong, China.
Frontiers in immunology
|June 2, 2023
概括
在癌症患者中,高水平的可溶性编程细胞死亡配体1 (shPD-L1) 促进T细胞抑制和免疫逃逸. 这解释了与shPD-L1相关的不良预后,并为精确免疫疗法开发提供了信息.
科学领域:
- 免疫学 免疫学 免疫学
- 癌症生物学 癌症生物学
- 分子生物学分子生物学
背景情况:
- 可溶性人类编程细胞死亡配体1 (shPD-L1) 与癌症预后不佳有关.
- 对于shPD-L1促进癌症进展的机制尚不清楚.
研究的目的:
- 研究癌症患者中shPD-L1和T细胞亡之间的相关性.
- 为了确定shPD-L1对T细胞功能和调节性T细胞生产的影响.
主要方法:
- 对癌症患者的shPD-L1水平和T细胞亡的分析.
- 在体外实验中评估shPD-L1对外周血液单核细胞 (PBMC) 增殖,细胞因子分泌和细胞毒性活性的影响.
- 评估shPD-L1在诱导T调节细胞中的作用.
主要成果:
- 在癌症患者中,PD-1+CD4+T细胞的亡升高,与shPD-L1水平呈正相关.
- shPD-L1抑制了PBMC的增殖,细胞因子的产生和杀死癌细胞的活动.
- shPD-L1促进了CD4+ T细胞转化为诱导的表达FoxP3.3的T调节细胞.
结论:
- shPD-L1抑制了激活的T细胞功能,并促进了对瘤细胞的周围耐受性.
- shPD-L1有助于全身瘤免疫逃逸,解释了它与预后的负相关性.
- 了解shPD-L1的外围作用对于开发用于各种癌症的精密免疫疗法至关重要.
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