Congress : ASGCT, Washington, USA, May 2019

T-cells represent valuable tools for treatment of cancers, infectious or inherited diseases but they are mainly short-lived in vivo.  T-cell therapies would strongly benefit from gene transfer into long-lived persisting naive T cells or T-cell progenitors. During the ASGCT 2019 congress (Washington 2019), INSERM partner presented latest published data on the generation of efficient gene-corrected T-cell progenitors from SCID patients.

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