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通过共表达网络分析确定老年人对四价灭活流感疫苗免疫反应中的潜在候选枢纽基因和功能富集通路

Identifying Potential Candidate Hub Genes and Functionally Enriched Pathways in the Immune Responses to Quadrivalent Inactivated Influenza Vaccines in the Elderly Through Co-Expression Network Analysis.

作者信息

Yang Jing, Zhang Jiayou, Fan Renfeng, Zhao Wei, Han Tian, Duan Kai, Li Xinguo, Zeng Peiyu, Deng Jinglong, Zhang Jikai, Yang Xiaoming

机构信息

National Institute of Engineering Technology Research in Combination Vaccine, Wuhan, China.

Wuhan Institute of Biological Products Co., Ltd., Wuhan, China.

出版信息

Front Immunol. 2020 Dec 4;11:603337. doi: 10.3389/fimmu.2020.603337. eCollection 2020.

DOI:10.3389/fimmu.2020.603337
PMID:33343577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7746648/
Abstract

Insights into the potential candidate hub genes may facilitate the generation of safe and effective immunity against seasonal influenza as well as the development of personalized influenza vaccines for the elderly at high risk of influenza virus infection. This study aimed to identify the potential hub genes related to the immune induction process of the 2018/19 seasonal quadrivalent inactivated influenza vaccines (QIVs) in the elderly ≥60 years by using weighted gene co-expression network analysis (WGCNA). From 63 whole blood samples from16 elderly individuals, a total of 13,345 genes were obtained and divided into eight co-expression modules, with two modules being significantly correlated with vaccine-induced immune responses. After functional enrichment analysis, genes under GO terms of vaccine-associated immunity were used to construct the sub-network for identification and functional validation of hub genes. and were confirmed as the hub genes with an obvious effect on QIVs-induced immunity. The expression was shown to be negatively correlated with the QIVs-associated reactogenicity within 7 days after vaccination, which could be suppressed by the CXCL 8/IL-8 and exacerbated by the Granzyme-B cytotoxic mediator. Meanwhile, the expression was found to increase the immune responses to the QIVs and contribute to the persistence of protective humoral antibody titers. These two genes can be used to predict QIVs-induced adverse reaction, the intensity of immune responses, and the persistence of humoral antibody against influenza. This work has shed light on further research on the development of personalized QIVs with appropriate immune responses and long-lasting immunity against the forthcoming seasonal influenza.

摘要

深入了解潜在的候选枢纽基因,可能有助于产生针对季节性流感的安全有效的免疫力,以及为流感病毒感染高危的老年人开发个性化流感疫苗。本研究旨在通过加权基因共表达网络分析(WGCNA),识别60岁及以上老年人中与2018/19季节性四价灭活流感疫苗(QIVs)免疫诱导过程相关的潜在枢纽基因。从16名老年人的63份全血样本中,共获得13345个基因,并将其分为8个共表达模块,其中两个模块与疫苗诱导的免疫反应显著相关。经过功能富集分析,利用与疫苗相关免疫的GO术语下的基因构建子网,以识别和功能验证枢纽基因。 和 被确认为对QIVs诱导的免疫有明显影响的枢纽基因。 表达显示与接种疫苗后7天内QIVs相关的反应原性呈负相关,可被CXCL 8/IL-8抑制,并被颗粒酶B细胞毒性介质加剧。同时,发现 表达可增强对QIVs的免疫反应,并有助于保护性体液抗体滴度的持续存在。这两个基因可用于预测QIVs诱导的不良反应、免疫反应强度以及针对流感的体液抗体的持续存在。这项工作为进一步研究开发具有适当免疫反应和对即将到来的季节性流感具有持久免疫力的个性化QIVs提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e44/7746648/4cff35b68156/fimmu-11-603337-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e44/7746648/cc9edbd0cd38/fimmu-11-603337-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e44/7746648/4cff35b68156/fimmu-11-603337-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e44/7746648/cc9edbd0cd38/fimmu-11-603337-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e44/7746648/218a2a0b356e/fimmu-11-603337-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e44/7746648/4cff35b68156/fimmu-11-603337-g007.jpg

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