流行性腮腺炎疫苗细胞免疫反应的多基因预测。

IF 5 3区 医学 Q1 GENETICS & HEREDITY
Brandon J Coombes, Inna G Ovsyannikova, Daniel J Schaid, Nathaniel D Warner, Gregory A Poland, Richard B Kennedy
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引用次数: 0

摘要

在本报告中,我们对先前发表的一项全基因组关联研究(GWAS)进行了随访分析,该研究评估了遗传多态性对细胞介导的腮腺炎疫苗免疫反应的个体间差异的影响。在这里,我们报告了多基因评分(PGS)分析的结果,显示了常见变异如何预测腮腺炎疫苗反应。我们发现较高的IFNγ、IL-2和TNFα的PGS分别预示着较高的疫苗后IFNγ (p值= 2e-6)、IL-2 (p = 2e-7)和TNFα (p = 0.004)水平。疫苗接种后免疫反应的控制是复杂和多基因的。我们的研究结果表明,基于pgs的方法能够更好地捕获有助于腮腺炎疫苗诱导免疫的综合遗传效应,可能比传统的单变体GWAS提供更全面的理解。这种方法可能在研究对其他疫苗和传染病的免疫反应的遗传控制方面具有广泛的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polygenic prediction of cellular immune responses to mumps vaccine.

In this report, we provide a follow-up analysis of a previously published genome-wide association study (GWAS) evaluating the effect of genetic polymorphisms on inter-individual variations in cell-mediated immune responses to mumps vaccine. Here we report the results of a polygenic score (PGS) analysis showing how common variants can predict mumps vaccine response. We found higher PGS for IFNγ, IL-2, and TNFα were predictive of higher post-vaccine IFNγ (p value = 2e-6), IL-2 (p = 2e-7), and TNFα (p = 0.004) levels, respectively. Control of immune responses after vaccination is complex and polygenic in nature. Our results suggest that the PGS-based approach enables better capture of the combined genetic effects that contribute to mumps vaccine-induced immunity, potentially offering a more comprehensive understanding than traditional single-variant GWAS. This approach will likely have broad utility in studying genetic control of immune responses to other vaccines and to infectious diseases.

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来源期刊
Genes and immunity
Genes and immunity 医学-免疫学
CiteScore
8.90
自引率
4.00%
发文量
28
审稿时长
6-12 weeks
期刊介绍: Genes & Immunity emphasizes studies investigating how genetic, genomic and functional variations affect immune cells and the immune system, and associated processes in the regulation of health and disease. It further highlights articles on the transcriptional and posttranslational control of gene products involved in signaling pathways regulating immune cells, and protective and destructive immune responses.
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