从出生到老年的血液组织中统一的高分辨率免疫细胞分数估计。

IF 10.4 1区 生物学 Q1 GENETICS & HEREDITY
Xiaolong Guo, Mahnoor Sulaiman, Alexander Neumann, Shijie C Zheng, Charlotte A M Cecil, Andrew E Teschendorff, Bastiaan T Heijmans
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引用次数: 0

摘要

免疫细胞组分的变化可能混淆或阻碍血液中基于dna的生物标志物的解释。虽然细胞型反褶积可以解决脐带血和成人血的这一挑战,但目前还没有适用于其他年龄组(包括婴儿和儿童)血液的方法。在这里,我们构建并广泛验证了一个名为UniLIFE的dna参考面板,用于19种免疫细胞类型,适用于任何年龄的血液组织。我们使用UniLIFE来描述从出生到老年的免疫细胞组分的动态,并推断新生儿、婴儿、儿童和成人中与疾病相关的免疫细胞组分的变化。在一项针对婴儿和儿童1型糖尿病的前瞻性纵向研究中,UniLIFE确定了1型糖尿病诊断之前的差异甲基化位点,并映射到糖尿病相关的信号通路。总之,UniLIFE将改进对任何年龄组的血液dna生物标志物的识别和解释,特别是对包括婴儿和儿童在内的纵向研究。我们的EpiDISH Bioconductor R-package提供UniLIFE面板和算法来估计细胞类型分数:https://bioconductor.org/packages/release/bioc/html/EpiDISH.html。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unified high-resolution immune cell fraction estimation in blood tissue from birth to old age.

Variations in immune-cell fractions can confound or hamper interpretation of DNAm-based biomarkers in blood. Although cell-type deconvolution can address this challenge for cord and adult blood, currently there is no method applicable to blood from other age groups, including infants and children. Here we construct and extensively validate a DNAm reference panel, called UniLIFE, for 19 immune cell-types, applicable to blood tissue of any age. We use UniLIFE to delineate the dynamics of immune-cell fractions from birth to old age, and to infer disease associated immune cell fraction variations in newborns, infants, children and adults. In a prospective longitudinal study of type-1 diabetes in infants and children, UniLIFE identifies differentially methylated positions that precede type-1 diabetes diagnosis and that map to diabetes related signaling pathways. In summary, UniLIFE will improve the identification and interpretation of blood-based DNAm biomarkers for any age group, but specially for longitudinal studies that include infants and children. The UniLIFE panel and algorithms to estimate cell-type fractions are available from our EpiDISH Bioconductor R-package: https://bioconductor.org/packages/release/bioc/html/EpiDISH.html.

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来源期刊
Genome Medicine
Genome Medicine GENETICS & HEREDITY-
CiteScore
20.80
自引率
0.80%
发文量
128
审稿时长
6-12 weeks
期刊介绍: Genome Medicine is an open access journal that publishes outstanding research applying genetics, genomics, and multi-omics to understand, diagnose, and treat disease. Bridging basic science and clinical research, it covers areas such as cancer genomics, immuno-oncology, immunogenomics, infectious disease, microbiome, neurogenomics, systems medicine, clinical genomics, gene therapies, precision medicine, and clinical trials. The journal publishes original research, methods, software, and reviews to serve authors and promote broad interest and importance in the field.
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