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A new approach to CAR T cell gene engineering using piggyBac transposon and cultivation in the presence of IL-4, IL-7 and IL-21

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F18%3A00011906" target="_blank" >RIV/00023736:_____/18:00011906 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1016/j.jcyt.2017.10.001" target="_blank" >https://doi.org/10.1016/j.jcyt.2017.10.001</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jcyt.2017.10.001" target="_blank" >10.1016/j.jcyt.2017.10.001</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A new approach to CAR T cell gene engineering using piggyBac transposon and cultivation in the presence of IL-4, IL-7 and IL-21

  • Original language description

    Clinical-grade CAR19 T cells are routinely manufactured by lentiviral/retroviral (LV/RV) transduction of an anti-CD3/CD28 activated T cells which are then propagated in a culture medium supplemented with IL-2. The use of LV/RVs for T cell modification represents a manufacturing challenge due to the complexity of the transduction approach and the necessity of a thorough quality control.
We present here a significantly improved protocol for CAR19 T cell manufacture which is based on the electroporation of PBMCs with plasmid DNA encoding the piggyBac transposon/transposase vectors and their cultivation in the presence of cytokines IL-4, IL-7 and IL-21. We found that activation of CAR receptor either by its cognate ligand (i.e. CD19 expressed on the surface of B cells) or by anti-CAR antibody followed by cultivation in the presence of cytokines IL-4 and IL-7 enables strong and highly selective expansion of functional CAR19 T cells resulting in more than 90% CAR+T cells.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30205 - Hematology

Result continuities

  • Project

    <a href="/en/project/NV15-34498A" target="_blank" >NV15-34498A: Development of methods for cellular and gene therapy of hematological malignancies.</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Cytotherapy: the journal of cell therapy

  • ISSN

    1465-3249

  • e-ISSN

  • Volume of the periodical

    20

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    14

  • Pages from-to

    507-520

  • UT code for WoS article

    000430446900003

  • EID of the result in the Scopus database

    2-s2.0-85042195710