Ho Nguyen Huong Jenny Giang, Talvard-Balland Nana, Köhler Natalie, Zeiser Robert
Department of Hematology, Oncology and Stem Cell Transplantation, Faculty of Medicine, Freiburg University Medical Center, Freiburg, Germany.
CIBSS - Centre for Integrative Biological Signaling Studies, Freiburg, Germany.
Blood Cancer Discov. 2025 May 5;6(3):168-181. doi: 10.1158/2643-3230.BCD-24-0063.
We discuss the mechanisms of AML immune evasion including loss or downregulation of MHC class I and II, reduced TRAIL receptor expression, inhibitory metabolite production, inhibitory ligand expression, impaired proinflammatory cytokine production, and AML niche alterations.
我们讨论了急性髓系白血病(AML)免疫逃逸的机制,包括主要组织相容性复合体(MHC)I类和II类的缺失或下调、肿瘤坏死因子相关凋亡诱导配体(TRAIL)受体表达降低、抑制性代谢产物产生、抑制性配体表达、促炎细胞因子产生受损以及AML微环境改变。