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表观遗传漂变与乙肝疫苗接种效果有关。

Epigenetic Drift Is Involved in the Efficacy of HBV Vaccination.

作者信息

Ferraresi Francesca, Anticoli Simona, Salvioli Stefano, Pirazzini Chiara, Calzari Luciano, Gentilini Davide, Albano Christian, Di Prinzio Reparata Rosa, Zaffina Salvatore, Carsetti Rita, Garagnani Paolo, Ruggieri Anna, Kwiatkowska Katarzyna Malgorzata

机构信息

Department of Chemistry "Giacomo Ciamician", University of Bologna, 40126 Bologna, Italy.

Istituto Superiore di Sanità, Center for Gender Specific Medicine, 00161 Rome, Italy.

出版信息

Vaccines (Basel). 2024 Nov 27;12(12):1330. doi: 10.3390/vaccines12121330.

Abstract

: HBV infections can lead to serious liver complications that can have fatal consequences. In 2022, around 1.1 million individuals died from HBV-related cirrhosis and hepatocellular carcinoma. Vaccines allow us to save more than 2.5 million lives each year; however, up to 10% of vaccinated individuals may not develop sufficient protective antibody levels. The aim of this study was to investigate the epigenetic drift in the response to HBV vaccine in isolated B cells. : Epigenetic drift was measured by counting rare DNA methylation variants. These epivariants were detected in epigenome-wide data collected from isolated B cell samples from 41 responders and 30 non-responders (age range 22-62 years) to vaccination against HBV. : We found an accumulation of epivariants in the NR group, with a significant increase in hyper-methylated aberrations. We identified the chromosomes (1, 3, 11, 12, and 14) and genes (e.g., or ) particularly enriched in epivariants in NRs. The literature search and pathway analysis indicate that such genes are involved in the correct functioning of the immune system. Moreover, we observed a correlation between epigenetic drift and DNA methylation entropy in the male population of the cohort. Finally, we confirmed the correlation between epivariant loads and age-related epigenetic clocks. : Our findings support the idea that an age-related derangement of the epigenetic architecture is involved in unresponsiveness to the HBV vaccine. Furthermore, the overall results highlight the interconnection between various epigenetic dynamics (such as drift, clocks, and entropy), although these interconnections seem not to be involved in the altered immunological activity.

摘要

乙肝病毒(HBV)感染可导致严重的肝脏并发症,甚至可能产生致命后果。2022年,约110万人死于与HBV相关的肝硬化和肝细胞癌。疫苗每年能挽救超过250万人的生命;然而,高达10%的接种疫苗个体可能无法产生足够的保护性抗体水平。本研究的目的是调查分离的B细胞对HBV疫苗反应中的表观遗传漂移。

通过计数罕见的DNA甲基化变异来测量表观遗传漂移。这些表观遗传变异在从41名接种HBV疫苗的应答者和30名无应答者(年龄范围22 - 62岁)的分离B细胞样本中收集的全基因组表观遗传数据中被检测到。

我们发现无应答组中表观遗传变异的积累,高甲基化畸变显著增加。我们确定了在无应答者中表观遗传变异特别富集的染色体(1、3、11、12和14)和基因(例如 或 )。文献检索和通路分析表明,这些基因参与免疫系统的正常功能。此外,我们在队列的男性人群中观察到表观遗传漂移与DNA甲基化熵之间的相关性。最后,我们证实了表观遗传变异负荷与年龄相关的表观遗传时钟之间的相关性。

我们的研究结果支持这样一种观点,即与年龄相关的表观遗传结构紊乱与对HBV疫苗无应答有关。此外,总体结果突出了各种表观遗传动力学(如漂移、时钟和熵)之间的相互联系,尽管这些相互联系似乎与免疫活性改变无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39a2/11680278/491781bf13e9/vaccines-12-01330-g001.jpg

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