Pre-existing intratumoral stem-like CD8+ T cells drive radiotherapy-induced tumor immunity

CD8<sup>+</sup> T cells are crucial for both spontaneous and therapy-induced restriction of tumor progression. Although many patients with cancer undergo radiotherapy, the precise effect of this genotoxic treatment on tumor-associated CD8<sup>+</sup> T cells is insufficiently understood. Here, we investigated the influence of radiotherapy on intratumoral CD8<sup>+</sup> T cells. We found that, although these CD8<sup>+</sup> T cells initially decline following radiotherapy, they subsequently expand and are both essential and sufficient for early tumor control. In response to radiotherapy, stem-like CD8<sup>+</sup> T cells proliferate and differentiate into effector CD8<sup>+</sup> T cells, making them key drivers of tumor immunity. Our findings underscore the pivotal role of intratumoral stem-like CD8<sup>+</sup> T cells in mediating radiotherapy-induced anti-tumor immunity and provide deeper insights into the dynamic behavior of CD8<sup>+</sup> T cells during tumor control after radiotherapy.

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Publication Details

Journal
Cell Reports
Published
2025-04-01
DOI
https://doi.org/10.1016/j.celrep.2025.115566
Citations
2
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
2.09
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article

Pre-existing intratumoral stem-like CD8+ T cells drive radiotherapy-induced tumor immunity

Virginia Cecconi, Maries van den Broek, Marc Nater, Cheïma Boudjeniba et al.
2 citations
Cell Reports
Cancer Immunotherapy and Biomarkers
2.09
article

Pre-existing intratumoral stem-like CD8+ T cells drive radiotherapy-induced tumor immunity

Virginia Cecconi, Maries van den Broek, Marc Nater, Cheïma Boudjeniba, Hakan Köksal, Paulo Perreira, M. Herbst, Nicola Regli, Nese Erdem Borgoni
article en
2 citations

Abstract

CD8<sup>+</sup> T cells are crucial for both spontaneous and therapy-induced restriction of tumor progression. Although many patients with cancer undergo radiotherapy, the precise effect of this genotoxic treatment on tumor-associated CD8<sup>+</sup> T cells is insufficiently understood. Here, we investigated the influence of radiotherapy on intratumoral CD8<sup>+</sup> T cells. We found that, although these CD8<sup>+</sup> T cells initially decline following radiotherapy, they subsequently expand and are both essential and sufficient for early tumor control. In response to radiotherapy, stem-like CD8<sup>+</sup> T cells proliferate and differentiate into effector CD8<sup>+</sup> T cells, making them key drivers of tumor immunity. Our findings underscore the pivotal role of intratumoral stem-like CD8<sup>+</sup> T cells in mediating radiotherapy-induced anti-tumor immunity and provide deeper insights into the dynamic behavior of CD8<sup>+</sup> T cells during tumor control after radiotherapy.

Cell ReportsVol. 44(4)
Institut Pasteur (FR), University of Zurich (CH), Université Paris Cité (FR)
Good health and well-being
Openalex Percentile: Top 13%
Cancer Immunotherapy and Biomarkers
2.09
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