Immunology Research Area, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Department of Pediatric Hematology/Oncology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Front Immunol. 2021 Apr 27;12:657329. doi: 10.3389/fimmu.2021.657329. eCollection 2021.
A recent approach of hematopoietic stem cell (HSC) transplantation from haploidentical donors "mobilized" with G-CSF is based on the selective depletion of T and B lymphocytes from the graft. Through this approach, the patient receives both HSC and mature donor-derived effector cells (including NK cells), which exert both anti-leukemia activity and protection against infections. We previously showed that donor HSC mobilization with G-CSF results in accumulation in the graft of polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs), capable of inhibiting the anti-leukemia activity of allogeneic NK cells. Here, we performed a detailed gene expression analysis on NK cells and PMN-MDSCs both derived from mobilized graft. Cytotoxicity assays and real time PCR arrays were performed in NK cells. Microarray technology followed by bioinformatics analysis was used for gene expression profiling in PMN-MDSCs. Results indicate that NK cells from the graft have a lower cytolytic activity as compared to those from non-mobilized samples. Further, mobilized PMN-MDSCs displayed a peculiar transcriptional profile distinguishing them from non-mobilized ones. Differential expression of pro-proliferative and immune-modulatory genes was detected in mobilized PMN-MDSCs. These data strengthen the concept that G-CSF-mobilized PMN-MDSCs present in the graft display unique molecular characteristics, in line with the strong inhibitory effect on donor NK cells.
最近,一种来自用 G-CSF“动员”的单倍体供体的造血干细胞 (HSC) 移植方法是基于从移植物中选择性耗尽 T 和 B 淋巴细胞。通过这种方法,患者既接受 HSC,也接受成熟的供体衍生效应细胞(包括 NK 细胞),这些细胞既具有抗白血病活性,又能预防感染。我们之前表明,用 G-CSF 动员供体 HSC 会导致移植物中积累多形核髓系来源的抑制细胞 (PMN-MDSCs),这些细胞能够抑制同种异体 NK 细胞的抗白血病活性。在这里,我们对来自动员移植物的 NK 细胞和 PMN-MDSCs 进行了详细的基因表达分析。在 NK 细胞中进行了细胞毒性测定和实时 PCR 阵列分析。使用微阵列技术和生物信息学分析对 PMN-MDSCs 进行基因表达谱分析。结果表明,与非动员样本相比,移植物中的 NK 细胞的细胞毒性活性较低。此外,动员的 PMN-MDSCs 表现出独特的转录谱,将其与非动员的 PMN-MDSCs 区分开来。在动员的 PMN-MDSCs 中检测到促增殖和免疫调节基因的差异表达。这些数据进一步证实了 G-CSF 动员的 PMN-MDSCs 在移植物中显示出独特的分子特征,与对供体 NK 细胞的强烈抑制作用一致。