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 language | English |
|---|---|
| Article number | 3168 |
| Journal | Cancers |
| Volume | 14 |
| Issue number | 13 |
| DOIs | |
| Publication status | Published - 1 Jul 2022 |
| Externally published | Yes |
Keywords
- CAR-T cells
- CD123
- Umbilical Cord Blood
- adoptive cell therapy
- allogeneic immunotherapy
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