免疫疗法
肺癌
医学
癌症免疫疗法
T细胞
免疫学
转录组
CXCL13型
癌症
生物
癌症研究
肿瘤科
内科学
免疫系统
基因表达
基因
趋化因子
遗传学
趋化因子受体
作者
Michelle Brennan,David DeBruin,Chinye Nwokolo,Katey S. Hunt,Alexander Piening,Maureen J. Donlin,Stephen T. Ferris,Ryan M. Teague,Richard J. DiPaolo,Elise Alspach
出处
期刊:Cancer immunology research
[American Association for Cancer Research]
日期:2024-05-02
卷期号:12 (8): 956-963
被引量:2
标识
DOI:10.1158/2326-6066.cir-23-0826
摘要
Abstract Emerging evidence in preclinical models demonstrates that antitumor immunity is not equivalent between males and females. However, more investigation in patients and across a wider range of cancer types is needed to fully understand sex as a variable in tumor immune responses. We investigated differences in T-cell responses between male and female patients with lung cancer by performing sex-based analysis of single cell transcriptomic datasets. We found that the transcript encoding CXC motif chemokine ligand 13 (CXCL13), which has recently been shown to correlate with T-cell tumor specificity, is expressed at greater levels in T cells isolated from female compared with male patients. Furthermore, increased CXCL13 expression was associated with response to PD1–targeting immunotherapy in female but not male patients. These findings suggest that there are sex-based differences in T-cell function required for response to anti–PD1 therapy in lung cancer that may need to be considered during patient treatment decisions. See related Spotlight by Cruz-Hinojoza and Stromnes, p. 952
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