<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(34)</volume><submitter>Lu H</submitter><pubmed_abstract>Radiation therapy (RT) is essential for treating thoracic malignancies but often causes significant lung damage. FLASH-RT, an ultra-high dose rate irradiation technique, shows potential in reducing radiation-induced lung injury (RILI) while maintaining tumor control. However, the underlying immune mechanisms remain poorly understood. This study investigates the immune and cellular responses to FLASH-RT versus conventional dose rate (CONV) RT during the early phase of RILI. Using single-cell RNA sequencing (scRNA-seq), a dynamic landscape of the lung microenvironment is pictured during RILI within one-week post-irradiation. The analysis reveals that FLASH-RT induces a more immediate but transient cellular response, while CONV-RT causes sustained inflammation. FLASH irradiation significantly</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pagination>e01797</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12442706</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>FLASH Irradiation Modulates Immune Responses and Accelerates Lung Recovery: A Single-Cell Perspective.</pubmed_title><pmcid>PMC12442706</pmcid><pubmed_authors>Dong G</pubmed_authors><pubmed_authors>Quan C</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Lu H</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Xu J</pubmed_authors></additional><is_claimable>false</is_claimable><name>FLASH Irradiation Modulates Immune Responses and Accelerates Lung Recovery: A Single-Cell Perspective.</name><description>Radiation therapy (RT) is essential for treating thoracic malignancies but often causes significant lung damage. FLASH-RT, an ultra-high dose rate irradiation technique, shows potential in reducing radiation-induced lung injury (RILI) while maintaining tumor control. However, the underlying immune mechanisms remain poorly understood. This study investigates the immune and cellular responses to FLASH-RT versus conventional dose rate (CONV) RT during the early phase of RILI. Using single-cell RNA sequencing (scRNA-seq), a dynamic landscape of the lung microenvironment is pictured during RILI within one-week post-irradiation. The analysis reveals that FLASH-RT induces a more immediate but transient cellular response, while CONV-RT causes sustained inflammation. FLASH irradiation significantly</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T11:31:34.333Z</modification><creation>2026-04-27T03:10:25.042Z</creation></dates><accession>S-EPMC12442706</accession><cross_references><pubmed>40536317</pubmed><doi>10.1002/advs.202501797</doi></cross_references></HashMap>