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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

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 8

Clinical SC-DARIC33 exhibits activity in patients following accurate targeting of rapamycin levels.

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Clinical SC-DARIC33 exhibits activity in patients following accurate tar...
(A) PLAT-08 clinical treatment schema. After SC-DARIC33 manufacturing, subjects receive lymphodepleting fludarabine and cyclophosphamide (Flu/Cy) and SC-DARIC33 at 1 of 3 assigned dose levels on day 0. Rapamycin is administered on days 3–21. Bone marrow biopsies are conducted for response assessments on days 21 and 28. (B) Simulated serum rapamycin concentrations using population pharmacokinetic modeling. Daily administration of 0.5 mg/m2 rapamycin achieves trough concentrations above the target range for SC-DARIC33 activation and peak concentrations below immunosuppressive doses of rapamycin for most pediatric subjects. (C) Characteristics of thawed clinical SC-DARIC33 cell products administered to trial participants. The proportion of cells expressing surface DARIC components as assessed by flow cytometry is shown. (D) Expression of activation markers by clinical infusion cell products following overnight culture in medium alone or medium supplemented with 1 nM rapamycin. (E) Frequent reevaluation enables successful targeting of serum rapamycin levels in patients. The proportion of time points (both peak and trough levels) within the target range (1.5–4 ng/mL) is shown at right. (F) Elevation of serum cytokines associated with T cell activation is observed following administration of SC-DARIC33. Traces show cytokine levels for samples obtained from each patient. Values reported are the mean of n = 2 replicates.

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