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Umbilical Cord Blood as a Source of Less Differentiated T cells to Produce CD123 CAR-T Cells

  • Blandine Caël
  • , Jeanne Galaine
  • , Isabelle Bardey
  • , Chrystel Marton
  • , Maxime Fredon
  • , Sabeha Biichle
  • , Margaux Poussard
  • , Yann Godet
  • , Fanny Angelot-Delettre
  • , Christophe Barisien
  • , Christophe Bésiers
  • , Olivier Adotevi
  • , Fabienne Pouthier
  • , Francine Garnache-Ottou
  • , Elodie Bôle-Richard*
  • *Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

29 Citations (Scopus)

Abstract

Chimeric Antigen Receptor (CAR) therapy has led to great successes in patients with leukemia and lymphoma. Umbilical Cord Blood (UCB), stored in UCB banks, is an attractive source of T cells for CAR-T production. We used a third generation CD123 CAR-T (CD28/4-1BB), which was previously developed using an adult’s Peripheral Blood (PB), to test the ability of obtaining CD123 CAR-T from fresh or cryopreserved UCB. We obtained a cell product with a high and stable trans-duction efficacy, and a poorly differentiated phenotype of CAR-T cells, while retaining high cyto-toxic functions in vitro and in vivo. Moreover, CAR-T produced from cryopreserved UCB are as functional as CAR-T produced from fresh UCB. Overall, these data pave the way for the clinical development of UCB-derived CAR-T. UCB CAR-T could be transferred in an autologous manner (after an UCB transplant) to reduce post-transplant relapses, or in an allogeneic setting, thanks to fewer HLA restrictions which ease the requirements for a match between the donor and recipient.

Original languageEnglish
Article number3168
JournalCancers
Volume14
Issue number13
DOIs
Publication statusPublished - 1 Jul 2022
Externally publishedYes

Keywords

  • CAR-T cells
  • CD123
  • Umbilical Cord Blood
  • adoptive cell therapy
  • allogeneic immunotherapy

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