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Drug-regulated CD33-targeted CAR T cells control AML using clinically optimized rapamycin dosing
Jacob Appelbaum, … , Alexander Astrakhan, Michael C. Jensen
Jacob Appelbaum, … , Alexander Astrakhan, Michael C. Jensen
Published March 19, 2024
Citation Information: J Clin Invest. 2024;134(9):e162593. https://doi.org/10.1172/JCI162593.
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Research Article Hematology Article has an altmetric score of 5

Drug-regulated CD33-targeted CAR T cells control AML using clinically optimized rapamycin dosing

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Abstract

Chimeric antigen receptor (CAR) designs that incorporate pharmacologic control are desirable; however, designs suitable for clinical translation are needed. We designed a fully human, rapamycin-regulated drug product for targeting CD33+ tumors called dimerizaing agent–regulated immunoreceptor complex (DARIC33). T cell products demonstrated target-specific and rapamycin-dependent cytokine release, transcriptional responses, cytotoxicity, and in vivo antileukemic activity in the presence of as little as 1 nM rapamycin. Rapamycin withdrawal paused DARIC33-stimulated T cell effector functions, which were restored following reexposure to rapamycin, demonstrating reversible effector function control. While rapamycin-regulated DARIC33 T cells were highly sensitive to target antigen, CD34+ stem cell colony-forming capacity was not impacted. We benchmarked DARIC33 potency relative to CD19 CAR T cells to estimate a T cell dose for clinical testing. In addition, we integrated in vitro and preclinical in vivo drug concentration thresholds for off-on state transitions, as well as murine and human rapamycin pharmacokinetics, to estimate a clinically applicable rapamycin dosing schedule. A phase I DARIC33 trial has been initiated (PLAT-08, NCT05105152), with initial evidence of rapamycin-regulated T cell activation and antitumor impact. Our findings provide evidence that the DARIC platform exhibits sensitive regulation and potency needed for clinical application to other important immunotherapy targets.

Authors

Jacob Appelbaum, April E. Price, Kaori Oda, Joy Zhang, Wai-Hang Leung, Giacomo Tampella, Dong Xia, Pauline P.L. So, Sarah K. Hilton, Claudya Evandy, Semanti Sarkar, Unja Martin, Anne-Rachel Krostag, Marissa Leonardi, Daniel E. Zak, Rachael Logan, Paula Lewis, Secil Franke-Welch, Njabulo Ngwenyama, Michael Fitzgerald, Niklas Tulberg, Stephanie Rawlings-Rhea, Rebecca A. Gardner, Kyle Jones, Angelica Sanabria, William Crago, John Timmer, Andrew Hollands, Brendan Eckelman, Sanela Bilic, Jim Woodworth, Adam Lamble, Philip D. Gregory, Jordan Jarjour, Mark Pogson, Joshua A. Gustafson, Alexander Astrakhan, Michael C. Jensen

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Figure 3

DARIC33 is specific for CD33 antigen and does not inhibit HSPC colony formation.

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DARIC33 is specific for CD33 antigen and does not inhibit HSPC colony fo...
(A and B) Evaluation of CD33-specific VHH-Fc fusion proteins used in DARIC33 designs. (A) Schematic depicting detection strategy of VHH-Fc fusions binding to HEK293 cells expressing one of 5,528 surface-bound or secreted proteins. After reverse transfection, HEK293 cells are spotted onto slides, then stained with VHH-Fc proteins (or PBS control) and Alexa Fluor 647–labeled anti–human Fc secondary antibodies. (B) Secondary screen of selected hit and control transgenic HEK293 samples (n = 2 replicates shown). (C) Stimulation of T cell IFN-γ release by DARIC33 designs in the presence of rapamycin following exposure to HEK293 cells electroporated with mRNA encoding CD33M (left) and CD33m (right). (D) Left: Stimulation of T cell IFN-γ release by DARIC33 designs in the presence of rapamycin following exposure to HEK293 cells electroporated with mRNA encoding Siglec-6. Right: Release of IFN-γ following coculture of DARIC33 with MV4-11 AML cells is shown for comparison. (E) Correlation of CD33 density (expressed as the logarithm of the antigen binding capacity) with release of IFN-γ (left) and IL-2 (right). (F) Colony-forming units following culture of CD34+ cells alone or with T cells in the presence or absence of rapamycin. Colonies were enumerated after 14 days of growth. n = 2 T cell donors. **P < 0.01, ****P < 0.0001, ANOVA with Tukey’s multiple-comparison correction.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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