American Association for Cancer Research
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Supplemental Figure 4 from Infusion Product TNFα, Th2, and STAT3 Activities Are Associated with Clinical Responses to Transgenic T-cell Receptor Cell Therapy

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posted on 2023-12-07, 17:00 authored by Theodore S. Nowicki, Cole W. Peters, Crystal Quiros, Conner K. Kidd, Moe Kawakami, Alexandra M. Klomhaus, Ignacio Baselga-Carretero, Paula Kaplan-Lefko, Mignonette H. Macabali, Ivan Perez Garcilazo, Beata Berent-Maoz, Begoña Comin-Anduix, Antoni Ribas

Contribution of all assayed secreted cytokines to CD8 cytokine polyfunctionality strength indices (PSI). Groups are divided by clinical response and tonic vs stimulated culture conditions. Error bars represent +/- standard error of the mean (SEM).


National Cancer Institute (NCI)

United States Department of Health and Human Services

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California Institute for Regenerative Medicine (CIRM)

Hyundai Hope On Wheels (Hope On Wheels)

Ruby Family Foundation

Parker Institute for Cancer Immunotherapy (Parker Institute)

Ressler Family Fund

Ken and Donna Schultz

Todd and Donna Jones

Thomas Stutz



Transgenic T-cell receptor (TCR) T cell–based adoptive cell therapies for solid tumors are associated with dramatic initial response rates, but there remain many instances of treatment failure and disease relapse. The association of infusion product cytokine profiles with clinical response has not been explored in the context of TCR T-cell therapy products. Single-cell antigen-dependent secretomic and proteomic analysis of preinfusion clinical TCR T-cell therapy products revealed that TNFα cytokine functionality of CD8+ T cells and phospho-STAT3 signaling in these cells were both associated with superior clinical responsiveness to therapy. By contrast, CD4+ T-helper 2 cell cytokine profiles were associated with inferior clinical responses. In parallel, preinfusion levels of IL15, Flt3-L, and CX3CL1 were all found to be associated with clinical response to therapy. These results have implications for the development of therapeutic biomarkers and identify potential targets for enrichment in the design of transgenic TCR T-cell therapies for solid tumors.

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