Max Von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Feodor-Lynen-Str. 23, 81377, Munich, Germany.
Department of Medicine III, University Hospital, LMU, Munich, Germany.
Clin Exp Med. 2024 Jul 13;24(1):155. doi: 10.1007/s10238-024-01425-w.
Knowledge of the molecular pathogenesis of acute myeloid leukemia has advanced in recent years. Despite novel treatment options, acute myeloid leukemia remains a survival challenge for elderly patients. We have recently shown that the triphosphohydrolase SAMHD1 is one of the factors determining resistance to Ara-C treatment. Here, we designed and tested novel and simpler virus-like particles incorporating the lentiviral protein Vpx to efficiently and transiently degrade SAMHD1 and increase the efficacy of Ara-C treatment. The addition of minute amounts of lentiviral Rev protein during production enhanced the generation of virus-like particles. In addition, we found that our 2nd generation of virus-like particles efficiently targeted and degraded SAMHD1 in AML cell lines with high levels of SAMHD1, thereby increasing Ara-CTP levels and response to Ara-C treatment. Primary AML blasts were generally less responsive to VLP treatment. In summary, we have been able to generate novel and simpler virus-like particles that can efficiently deliver Vpx to target cells.
近年来,人们对急性髓细胞白血病的分子发病机制有了更多的了解。尽管有新的治疗选择,老年患者的急性髓细胞白血病仍然是一个生存挑战。我们最近表明,三磷酸水解酶 SAMHD1 是决定对阿糖胞苷治疗耐药的因素之一。在这里,我们设计并测试了新型且更简单的病毒样颗粒,其中包含慢病毒蛋白 Vpx,可有效且短暂地降解 SAMHD1 并提高阿糖胞苷治疗的效果。在生产过程中添加少量慢病毒 Rev 蛋白可增强病毒样颗粒的生成。此外,我们发现我们的第二代病毒样颗粒能够有效地靶向和降解高水平 SAMHD1 的 AML 细胞系中的 SAMHD1,从而增加 Ara-CTP 水平并提高对阿糖胞苷治疗的反应。原代 AML blasts 对 VLP 治疗的反应通常较低。总之,我们已经能够生成新型且更简单的病毒样颗粒,能够有效地将 Vpx 递送到靶细胞。