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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 1

Rapamycin licenses permits antigen-dependent DARIC33 T cell responses and stabilizes surface expression of DARIC33 components.

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Rapamycin licenses permits antigen-dependent DARIC33 T cell responses an...
(A) Schematic depicting rapamycin-dependent activation of DARIC33. In the absence of rapamycin, the two DARIC components are split and do not respond to antigen. Following rapamycin addition, heterodimerization of DARIC components enables antigen-dependent T cell responses. (B) Schematic depicting generation of DARIC33 candidates and T cell production. DNA sequences encoding modified VHH sequences are incorporated into DARIC33 lentiviral expression vectors. (C) IFN-γ release by DARIC33 cell products following coculture with CD33+ MV4-11 AML cells. One of n = 3 donors is shown. ***P < 0.001, ANOVA with Tukey’s multiple-comparison correction. (D–F) Rapamycin stabilizes surface expression of DARIC33 components. DARIC33 cell products were cultured in medium alone or medium containing 1 nM rapamycin overnight before staining and evaluation by flow cytometry. Representative flow cytometry plots from 1 of 3 donors (above) with quantitation of percentage positive and median fluorescence intensity (MFI) from all 3 donors (below). *P < 0.05, **P < 0.01, ***P < 0.001, 2-way ANOVA with Šidák’s multiple-comparison correction, n = 3 donors. (D) Rapamycin increases antigen binding capacity of DARIC33 cells. (E) Rapamycin increases surface expression of the antigen signaling arm of DARIC. (F) Rapamycin increases surface expression of the antigen recognition arm of DARIC.

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

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