Preservation of T-Cell Stemness with a Novel Expansionless CAR-T Manufacturing Process, Which Reduces Manufacturing Time to Less Than Two Days, Drives Enhanced CAR-T Cell Efficacy

Background: Extended T-cell culture periods in vitro deplete the CAR-T final product of naive and stem cell memory T-cell (T scm) subpopulations that are associated with improved antitumor efficacy. YTB323 is an autologous CD19-directed CAR-T cell therapy with dramatically simplified manufacturing,...

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Veröffentlicht in:Blood 2021-11, Vol.138 (Supplement 1), p.2848-2848
Hauptverfasser: Engels, Boris, Zhu, Xu, Yang, Jennifer, Price, Andrew, Sohoni, Akash, Stein, Andrew M, Parent, Lana, Greene, Michael, Niederst, Matthew, Whalen, Jeanne, Orlando, Elena J, Treanor, Louise M, Brogdon, Jennifer L
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Sprache:eng
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Zusammenfassung:Background: Extended T-cell culture periods in vitro deplete the CAR-T final product of naive and stem cell memory T-cell (T scm) subpopulations that are associated with improved antitumor efficacy. YTB323 is an autologous CD19-directed CAR-T cell therapy with dramatically simplified manufacturing, which eliminates complexities such as long culture periods. This improved T-Charge™ process preserves T-cell stemness, an important characteristic closely tied to therapeutic potential, which leads to enhanced expansion ability and greater antitumor activity of CAR-T cells. Methods: The new T-Charge TM manufacturing platform, which reduces ex vivo culture time to about 24 hours and takes
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2021-146246