Martin Štach

ORCID: 0000-0003-0655-2706
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About
Contact & Profiles
Research Areas
  • CAR-T cell therapy research
  • Virus-based gene therapy research
  • Viral Infectious Diseases and Gene Expression in Insects
  • Immune Cell Function and Interaction
  • Polyomavirus and related diseases

Institute of Haematology and Blood Transfusion
2018-2024

Charles University
2020-2024

The piggyBac transposon system provides a non-viral alternative for cost-efficient and simple chimeric antigen receptor (CAR) T cell production. generation of clinical-grade CAR cells requires strict adherence to current good manufacturing practice (cGMP) standards. Unfortunately, the high costs commonly used lentiviral or retroviral vectors limit in many non-commercial academic institutions. Here, we present platform highly efficient CD19-specific (CAR19 cells) based on co-electroporation...

10.1016/j.omtm.2021.08.006 article EN cc-by-nc-nd Molecular Therapy — Methods & Clinical Development 2021-08-26

Tisagenlecleucel (tisa-cel) is a CD19 - specific CAR-T cell product approved for the treatment of relapsed/refractory (r/r) DLBCL or B-ALL. We have followed group patients diagnosed with childhood B-ALL ( n = 5), adult 2), and 25) who were treated tisa-cel under non-clinical trial conditions. The goal was to determine how intensive pretreatment affects produced cells, their in vivo expansion, outcome therapy. Multiparametric flow cytometry used analyze material manufacturing cells...

10.3389/pore.2023.1610914 article EN cc-by Pathology & Oncology Research 2023-04-20

Background The non-viral production of CAR-T cells through electroporation transposon DNA plasmids is an alternative approach to lentiviral/retroviral methods. This method particularly suitable for early-phase clinical trials involving novel types cells. primary disadvantage methods the lower efficiency compared viral-based methods, which becomes a limiting factor production, especially in chemotherapy-pretreated lymphopenic patients. Methods We describe good manufacturing practice...

10.3389/fimmu.2024.1415328 article EN cc-by Frontiers in Immunology 2024-08-13
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