Jintao Wu, Xiaocheng Mao, Xiaohua Liu, Junying Mao, Xianxin Yang, Xiangwu zhou, Lu Tianzhu, Yulong Ji, Zhao Li, Huijuan Xu
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We followed a standardized analytical approach for quality assurance, batch effect adjustments, and preliminary data processing. We discerned distinct T cell subsets and conducted differential gene expression analysis. Potential key genes and pathways were inferred from GO and Pathway enrichment analyses. Additionally, we implemented Mendelian randomization to probe the potential links between pivotal genes and lung adenocarcinoma susceptibility. Our findings underscored a notable reduction in mature CD8 + central memory T cells in both lung adenocarcinoma and COVID-19 cohorts relative to the control group. Notably, the downregulation of specific genes, such as TRGV9, could impede the immunological efficacy of CD8 + T cells. Comprehensive multi-omics assessment highlighted genetic aberrations in genes, including TRGV9, correlating with heightened lung adenocarcinoma risk. 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引用次数: 0
摘要
肺腺癌的发病率和死亡率都很高,是一个重大的健康问题。与此同时,COVID-19 大流行已成为全球公共卫生面临的严峻挑战。现有文献表明,T 细胞是细胞免疫的关键组成部分,在抗病毒和抗肿瘤反应中都不可或缺。然而,T 细胞在不同疾病状态下的细微变化及其功能尚未得到全面阐明。我们收集了肺腺癌患者、COVID-19 患者和健康对照者外周血单核细胞的转录组数据。我们采用标准化分析方法进行质量保证、批次效应调整和初步数据处理。我们发现了不同的 T 细胞亚群,并进行了差异基因表达分析。通过 GO 和通路富集分析推断出潜在的关键基因和通路。此外,我们还采用了孟德尔随机化方法来探究关键基因与肺腺癌易感性之间的潜在联系。我们的研究结果表明,与对照组相比,肺腺癌组和 COVID-19 组中成熟的 CD8 + 中心记忆 T 细胞明显减少。值得注意的是,特定基因(如 TRGV9)的下调可能会阻碍 CD8 + T 细胞的免疫功效。全面的多组学评估突显了与肺腺癌风险增加相关的基因畸变,包括TRGV9。通过严格的单细胞转录组分析,这项研究细致地描述了不同病理状态下T细胞亚群的变化,并通过综合多组学方法推断出关键的调控基因,为未来的功能研究奠定了坚实的基础。这项研究为研究多种疾病的病因提供了宝贵的视角,并推动了精准医学的发展。
Integrative single-cell analysis: dissecting CD8 + memory cell roles in LUAD and COVID-19 via eQTLs and Mendelian Randomization
Lung adenocarcinoma exhibits high incidence and mortality rates, presenting a significant health concern. Concurrently, the COVID-19 pandemic has emerged as a grave global public health challenge. Existing literature suggests that T cells, pivotal components of cellular immunity, are integral to both antiviral and antitumor responses. Yet, the nuanced alterations and consequent functions of T cells across diverse disease states have not been comprehensively elucidated. We gathered transcriptomic data of peripheral blood mononuclear cells from lung adenocarcinoma patients, COVID-19 patients, and healthy controls. We followed a standardized analytical approach for quality assurance, batch effect adjustments, and preliminary data processing. We discerned distinct T cell subsets and conducted differential gene expression analysis. Potential key genes and pathways were inferred from GO and Pathway enrichment analyses. Additionally, we implemented Mendelian randomization to probe the potential links between pivotal genes and lung adenocarcinoma susceptibility. Our findings underscored a notable reduction in mature CD8 + central memory T cells in both lung adenocarcinoma and COVID-19 cohorts relative to the control group. Notably, the downregulation of specific genes, such as TRGV9, could impede the immunological efficacy of CD8 + T cells. Comprehensive multi-omics assessment highlighted genetic aberrations in genes, including TRGV9, correlating with heightened lung adenocarcinoma risk. Through rigorous single-cell transcriptomic analyses, this investigation meticulously delineated variations in T cell subsets across different pathological states and extrapolated key regulatory genes via an integrated multi-omics approach, establishing a robust groundwork for future functional inquiries. This study furnishes valuable perspectives into the etiology of multifaceted diseases and augments the progression of precision medicine.
HereditasBiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.80
自引率
3.70%
发文量
0
期刊介绍:
For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.