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  4. Novel Vpx virus-like particles to improve cytarabine treatment response against acute myeloid leukemia
 
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2024
Journal Article
Title

Novel Vpx virus-like particles to improve cytarabine treatment response against acute myeloid leukemia

Abstract
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.
Author(s)
Nair, Ramya
Ludwig-Maximilians-Universität München
Salinas-Illarena, Alejandro
Ludwig-Maximilians-Universität München
Sponheimer, Monika
Klinikum der Universität München
Wullkopf, Inès
Ludwig-Maximilians-Universität München
Schreiber, Yannick
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Côrte-Real, João Vasco
Ludwig-Maximilians-Universität München
del Pozo Ben, Augusto
Ludwig-Maximilians-Universität München
Marterer, Helena
Ludwig-Maximilians-Universität München
Thomas, Dominique
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Geißlinger, Gerd  
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Cinatl, Jindrich
Universitätsklinikum Frankfurt
Subklewe, Marion S.
Klinikum der Universität München
Baldauf, Hanna ‑m
Ludwig-Maximilians-Universität München
Journal
Clinical and Experimental Medicine  
Funder
Universitätsklinikum Heidelberg
Open Access
DOI
10.1007/s10238-024-01425-w
Additional link
Full text
Language
English
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Keyword(s)
  • AML

  • Cytarabine

  • Resistance

  • SAMHD1

  • VLP

  • Vpx

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