原位
X射线
接种疫苗
黑色素瘤
材料科学
医学
病毒学
光学
癌症研究
物理
气象学
作者
Verdiana Trappetti,Cristian Fernández-Palomo,Prateek Arora,Marine Potez,Paolo Pellicioli,Jennifer Fazzari,Nahoko Shintani,Ismael Sánchez-González,Cheuk Ting Wu,Bettina de Breuyn Dietler,Nadia Mercader,Olga A. Martin,Stephan von Gunten,Vladislav Volarević,Valentin Djonov
标识
DOI:10.1016/j.canlet.2024.217326
摘要
Despite the recent progress, current treatment modalities are not able to eradicate cancer. We show that Microbeam Radiotherapy (MRT), an innovative type of Spatially Fractionated Radiotherapy, can control murine melanoma by activating the host's own immune system. The beneficial effects are very pronounced in comparison to uniform radiotherapy, traditionally employed in the clinic. Our results displayed that MRT increased antigen presentation, activating Cytotoxic T Lymphocytes (CTLs) which are essential to MRT's treatment efficacy in melanoma. Depletion of CTLs abrogated treatment response. Multiplex nucleic acid hybridization technology revealed key features of lymphocyte populations such as proliferation, differentiation, and ligand-receptor interactions. In addition, CTLs were shown to be essential for locoregional metastatic control and systemic abscopal effects confirmed by activation of antigen presenting cells and CTL trafficking in the tumour-draining lymph nodes. MRT induces a robust antitumour immune response, matching the characteristics of in situ vaccination, that could be exploited to treat a variety of treatment-resistant malignancies.
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