Author:
Nair Ramya,Salinas-Illarena Alejandro,Sponheimer Monika,Wullkopf Inès,Schreiber Yannick,Côrte-Real João Vasco,del Pozo Ben Augusto,Marterer Helena,Thomas Dominique,Geisslinger Gerd,Cinatl Jindrich,Subklewe Marion,Baldauf Hanna-Mari
Abstract
AbstractKnowledge 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.
Funder
Wilhelm Sander-Stiftung
Studienstiftung des deutschen Volkes
Joachim Herz Foundation
Bavarian Elite Graduate School “i-target”
Fraunhofer Cluster of Excellence for Immune mediated Diseases
Fundação para a Ciência e Tecnologia
Deutsche Forschungsgemeinschaft
Ludwig-Maximilians-Universität München
Publisher
Springer Science and Business Media LLC