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腮腺炎疫苗细胞免疫反应的多基因预测

Polygenic prediction of cellular immune responses to mumps vaccine.

作者信息

Coombes Brandon J, Ovsyannikova Inna G, Schaid Daniel J, Warner Nathaniel D, Poland Gregory A, Kennedy Richard B

机构信息

Division of Computational Biology, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.

Mayo Clinic Vaccine Research Group, Mayo Clinic, Rochester, MN, USA.

出版信息

Genes Immun. 2025 Jun 10. doi: 10.1038/s41435-025-00335-5.

DOI:10.1038/s41435-025-00335-5
PMID:40494895
Abstract

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.

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,该研究评估了基因多态性对腮腺炎疫苗细胞介导免疫反应个体间差异的影响。在此,我们报告一项多基因评分(PGS)分析的结果,展示常见变异如何预测腮腺炎疫苗反应。我们发现,IFNγ、IL-2和TNFα的较高PGS分别预测了疫苗接种后较高的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本质上是复杂且多基因的。我们的结果表明,基于PGS的方法能够更好地捕捉导致腮腺炎疫苗诱导免疫的综合遗传效应,可能比传统的单变异GWAS提供更全面的理解。这种方法在研究对其他疫苗和传染病的免疫反应的遗传控制方面可能具有广泛的用途。

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本文引用的文献

1
Uncovering associations between pre-existing conditions and COVID-19 Severity: A polygenic risk score approach across three large biobanks.揭示既往疾病与 COVID-19 严重程度之间的关联:三个大型生物库的多基因风险评分方法。
PLoS Genet. 2023 Dec 19;19(12):e1010907. doi: 10.1371/journal.pgen.1010907. eCollection 2023 Dec.
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Genome-wide determinants of cellular immune responses to mumps vaccine.腮腺炎疫苗细胞免疫反应的全基因组决定因素
Vaccine. 2023 Oct 20;41(44):6579-6588. doi: 10.1016/j.vaccine.2023.09.001. Epub 2023 Sep 29.
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The potential of polygenic scores to improve cost and efficiency of clinical trials.
多基因风险评分提高临床试验成本和效率的潜力。
Nat Commun. 2022 May 25;13(1):2922. doi: 10.1038/s41467-022-30675-z.
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Mumps virus-specific immune response outcomes and sex-based differences in a cohort of healthy adolescents.健康青少年队列中腮腺炎病毒特异性免疫应答结局和基于性别的差异。
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Personalized vaccinology: A review.个性化疫苗学:综述。
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Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine.CD46和IFI44L基因变异与麻疹疫苗中和抗体反应的全基因组关联研究。
Hum Genet. 2017 Apr;136(4):421-435. doi: 10.1007/s00439-017-1768-9. Epub 2017 Mar 13.
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Next-generation genotype imputation service and methods.下一代基因型填充服务和方法。
Nat Genet. 2016 Oct;48(10):1284-1287. doi: 10.1038/ng.3656. Epub 2016 Aug 29.