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Chimeric antigen receptor (CAR)-T cell quality and stemness are associated with responsiveness, durability, and memory formation, which benefit clinical responses. Autologous T cell starting material across patients with cancer is variable and CAR-T expansion or potency can fail during manufacture. Thus, strategies to develop allogeneic CAR-T platforms including the identification and expansion of T cell subpopulations that correspond with CAR-T potency are an active area of investigation. Here, we compared CAR-T cells generated from healthy adult peripheral blood T cells versus placental circulating T (P-T) cells.
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Natalia Ruggeri Barbaro
Theodore Drashansky
Kristina Tess
Journal for ImmunoTherapy of Cancer
Celularity (United States)
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Barbaro et al. (Mon,) studied this question.
www.synapsesocial.com/papers/68e71035b6db64358768994d — DOI: https://doi.org/10.1136/jitc-2023-008656