An orthogonal IL-2 and IL-2Rβ system drives persistence and activation of CAR T cells and clearance of bulky lymphoma

Paul‐Joseph Aspuria(Synthego (United States)), Sandro Vivona(Synthego (United States)), Michele Bauer(Synthego (United States)), Marie Semana(Synthego (United States)), Navneet Ratti(Synthego (United States)), Scott McCauley(Synthego (United States)), Romina Riener(Synthego (United States)), René de Waal Malefyt(Synthego (United States)), Deepti Rokkam(Synthego (United States)), Jan Emmerich(Synthego (United States)), Rob Kastelein(Synthego (United States)), Patrick J. Lupardus(Synthego (United States)), Martin Oft(Synthego (United States))
Science Translational Medicine
December 22, 2021
Cited by 82

Abstract

) and effector T cells. In preclinical models of human CAR-refractory lymphoma, STK-009 treatment resulted in systemic and intratumoral expansion and activation of hoRb-expressing anti–CD19-CD28ζ CAR T cells (SYNCAR). The orthogonal IL-2 receptor/ligand system delivers complete responses in large subcutaneous lymphomas, even with substantially reduced CAR T cell doses, by selectively expanding and activating CAR T cells in vivo. STK-009 withdrawal allowed normal CAR T cell contraction, thereby limiting CRS induced by tumor antigen–specific T cell activation. These data suggest that the orthogonal IL-2 receptor/ligand system provides the in vivo control necessary to maximize efficacy of CAR T therapies.


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