Immunology Unit, Department of Physiology, University of Extremadura, Caceres, Spain.
Immunol Cell Biol. 2012 Jan;90(1):109-15. doi: 10.1038/icb.2011.15. Epub 2011 Mar 8.
This study tested the hypothesis that the expression of CD112 and CD155 (DNAM-1 ligands) on leukemic blasts induces a decreased expression of the activating receptor DNAM-1 on natural killer (NK) cells from acute myeloid leukemia (AML) patients. DNAM-1 is a co-receptor involved in the activation of NK cell cytotoxicity after its interaction with its ligands CD112 and CD155 on target cells. Here we study the expression of DNAM-1 on NK cells and DNAM-1 ligands on blasts from AML patients stratified by age. The results demonstrate that NK cells from AML patients younger than 65 years have a reduced expression of DNAM-1 compared with age-matched controls. The analysis of DNAM-1 ligands showed a high expression of CD112 and CD155 on leukemic blasts. An inverse correlation between CD112 expression on leukemic blasts and DNAM-1 expression on NK cells was found. Furthermore, downregulation of DNAM-1 was induced on healthy donors' NK cells after in vitro culture with leukemic blasts expressing DNAM-1 ligands. In conclusion, these results support the hypothesis that receptor-ligand crosslinking downregulates DNAM-1 expression on NK cells from patients <65 years of age. Considering the relevance of DNAM-1 in NK recognition and killing of leukemic cells, the reduced expression of this receptor on NK cells from AML patients can represent an additional mechanism of tumor escape.
这项研究检验了这样一个假设,即白血病细胞上 CD112 和 CD155(DNAM-1 配体)的表达诱导急性髓系白血病(AML)患者自然杀伤(NK)细胞上激活受体 DNAM-1 的表达降低。DNAM-1 是一种共受体,在与靶细胞上的配体 CD112 和 CD155 相互作用后,参与 NK 细胞细胞毒性的激活。在这里,我们研究了按年龄分层的 AML 患者 NK 细胞上 DNAM-1 的表达和 NK 细胞上 DNAM-1 配体的表达。结果表明,与年龄匹配的对照组相比,年龄小于 65 岁的 AML 患者 NK 细胞的 DNAM-1 表达降低。DNAM-1 配体的分析显示,白血病细胞上高表达 CD112 和 CD155。在白血病细胞上 CD112 的表达与 NK 细胞上 DNAM-1 的表达之间发现了负相关。此外,在体外培养表达 DNAM-1 配体的白血病细胞后,健康供体 NK 细胞上的 DNAM-1 表达被下调。总之,这些结果支持了这样一个假设,即受体-配体交联会下调年龄<65 岁的患者 NK 细胞上的 DNAM-1 表达。鉴于 DNAM-1 在 NK 识别和杀伤白血病细胞中的相关性,AML 患者 NK 细胞上该受体的表达降低可能代表肿瘤逃逸的另一种机制。