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• W4312018503 abstract "T cells play a determining role in the immunomodulation and prognostic evaluation of cancer treatments relying on immune activation. While specific biomarkers determine the population and distribution of T cells in tumours, the in situ activity of T cells is less studied. Here we designed T-cell-targeting fusogenic liposomes to regulate and quantify the activity of T cells by exploiting their surface redox status as a chemical target. The T-cell-targeting fusogenic liposomes equipped with 2,2,6,6-tetramethylpiperidine (TEMP) groups neutralize reactive oxygen species protecting T cells from oxidation-induced loss of activity. Meanwhile, the production of paramagnetic 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) radicals allows magnetic resonance imaging quantification of the T cell activity. In multiple mouse models, the T-cell-targeting fusogenic liposomes led to efficient tumour inhibition and to early prediction of radiotherapy outcomes. This study uses a chemical targeting strategy to measure the in situ activity of T cells for cancer theranostics and may provide further understanding on engineering T cells for cancer treatment. Measuring the in situ activation status of T cells is important to gauge the efficacy of immunotherapy approaches. In this Article the authors design a chemical probe that binds to the T cell membrane and scavenges reactive oxygen species (ROS), preventing ROS-driven T cell exhaustion while serving as a magnetic resonance imaging probe to quantify T cell activity in tumours and predict radiotherapy outcomes." @default.
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• W4312018503 date "2022-12-19" @default.
• W4312018503 modified "2023-10-16" @default.
• W4312018503 title "Targeting the activity of T cells by membrane surface redox regulation for cancer theranostics" @default.
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• W4312018503 doi "https://doi.org/10.1038/s41565-022-01261-7" @default.
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