T-cell expression of CXCL13 is associated with immunotherapy response in a sex-dependent manner in patients with lung cancer

IF 8.1 1区 医学 Q1 IMMUNOLOGY
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
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引用次数: 0

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 to male patients. Furthermore, increased expression of CXCL13 was associated with response to PD-1–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–PD-1 therapy in lung cancer that may need to be considered during patient treatment decisions.
肺癌患者 T 细胞中 CXCL13 的表达与免疫疗法反应的性别依赖性有关
临床前模型的新证据表明,男性和女性的抗肿瘤免疫力并不相同。然而,要充分了解性别作为肿瘤免疫反应中的一个变量,还需要对患者和更广泛的癌症类型进行更多的调查。我们通过对单细胞转录组数据集进行基于性别的分析,研究了肺癌男女患者之间 T 细胞反应的差异。我们发现,与男性患者相比,编码 CXC motif 趋化因子配体 13(CXCL13)的转录本在女性患者分离出的 T 细胞中的表达水平更高。此外,CXCL13表达的增加与女性患者而非男性患者对PD-1靶向免疫疗法的反应有关。这些研究结果表明,肺癌患者对抗PD-1疗法产生反应所需的T细胞功能存在性别差异,患者在做出治疗决定时可能需要考虑到这一点。
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来源期刊
Cancer immunology research
Cancer immunology research ONCOLOGY-IMMUNOLOGY
CiteScore
15.60
自引率
1.00%
发文量
260
期刊介绍: Cancer Immunology Research publishes exceptional original articles showcasing significant breakthroughs across the spectrum of cancer immunology. From fundamental inquiries into host-tumor interactions to developmental therapeutics, early translational studies, and comprehensive analyses of late-stage clinical trials, the journal provides a comprehensive view of the discipline. In addition to original research, the journal features reviews and opinion pieces of broad significance, fostering cross-disciplinary collaboration within the cancer research community. Serving as a premier resource for immunology knowledge in cancer research, the journal drives deeper insights into the host-tumor relationship, potent cancer treatments, and enhanced clinical outcomes. Key areas of interest include endogenous antitumor immunity, tumor-promoting inflammation, cancer antigens, vaccines, antibodies, cellular therapy, cytokines, immune regulation, immune suppression, immunomodulatory effects of cancer treatment, emerging technologies, and insightful clinical investigations with immunological implications.
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