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爱泼斯坦-巴尔病毒而非巨细胞病毒的潜伏会加速儿童麻疹和风疹疫苗反应的衰退——一项瑞典出生队列的10年随访研究

Epstein-Barr Virus, but Not Cytomegalovirus, Latency Accelerates the Decay of Childhood Measles and Rubella Vaccine Responses-A 10-Year Follow-up of a Swedish Birth Cohort.

作者信息

Lasaviciute Gintare, Björkander Sophia, Carvalho-Queiroz Claudia, Hed Myrberg Ida, Nussbaum Bianca, Nilsson Caroline, Bemark Mats, Nilsson Anna, Sverremark-Ekström Eva, Saghafian-Hedengren Shanie

机构信息

Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden.

Department of Women's and Children's Health, Childhood Cancer Research Unit, Astrid Lindgren Children's Hospital, Karolinska Institutet, Stockholm, Sweden.

出版信息

Front Immunol. 2017 Dec 21;8:1865. doi: 10.3389/fimmu.2017.01865. eCollection 2017.

DOI:10.3389/fimmu.2017.01865
PMID:29312344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5742589/
Abstract

BACKGROUND

Epstein-Barr virus (EBV) and cytomegalovirus (CMV) are ubiquitous and persistent herpesviruses commonly acquired during childhood. Both viruses have a significant impact on the immune system, especially through mediating the establishment of cellular immunity, which keeps these viruses under control for life. Far less is known about how these viruses influence B-cell responses.

OBJECTIVES

To evaluate the impact of latent EBV and CMV infection on rubella- and measles-specific antibody responses as well as on the B-cell compartment in a prospective birth cohort followed during the first 10 years of life.

METHODS

IgG titers against rubella and measles vaccines were measured in plasma obtained from the same donors at 2, 5, and 10 years of age. Peripheral B-cell subsets were evaluated at 2 and 5 years of age. Factors related to optimal B-cell responses including IL-21 and CXCL13 levels in plasma were measured at all-time points.

RESULTS

EBV carriage in the absence of CMV associated with an accelerated decline of rubella and measles-specific IgG levels ( = 0.003 and  = 0.019, respectively, linear mixed model analysis), while CMV carriage in the absence of EBV associated with delayed IgG decay over time for rubella ( = 0.034). At 5 years of age, EBV but not CMV latency associated with a lower percentage of plasmablasts, but higher IL-21 levels in the circulation.

CONCLUSION

Our findings suggest that EBV carriage in the absence of CMV influences the B-cell compartment and the dynamics of antibody responses over time during steady state in the otherwise healthy host.

摘要

背景

爱泼斯坦-巴尔病毒(EBV)和巨细胞病毒(CMV)是普遍存在且持续感染的疱疹病毒,通常在儿童期感染。这两种病毒对免疫系统有重大影响,特别是通过介导细胞免疫的建立,从而使这些病毒在一生中都处于受控状态。关于这些病毒如何影响B细胞反应,人们了解得要少得多。

目的

在一个前瞻性出生队列中,评估潜伏性EBV和CMV感染对风疹和麻疹特异性抗体反应以及B细胞区室的影响,该队列在出生后的前10年进行随访。

方法

在2岁、5岁和10岁时,测量来自同一供体的血浆中针对风疹和麻疹疫苗的IgG滴度。在2岁和5岁时评估外周B细胞亚群。在所有时间点测量与最佳B细胞反应相关的因素,包括血浆中的IL-21和CXCL13水平。

结果

在没有CMV的情况下携带EBV与风疹和麻疹特异性IgG水平的加速下降相关(分别为=0.003和=0.019,线性混合模型分析),而在没有EBV的情况下携带CMV与风疹IgG随时间的衰减延迟相关(=0.034)。在5岁时,EBV而非CMV潜伏与浆母细胞百分比降低但循环中IL-21水平升高相关。

结论

我们的研究结果表明,在没有CMV的情况下携带EBV会影响健康宿主稳态期间B细胞区室以及抗体反应随时间的动态变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/b8ac1cf55688/fimmu-08-01865-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/0245b98ad2ee/fimmu-08-01865-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/d362478ab12e/fimmu-08-01865-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/e85db4f91f19/fimmu-08-01865-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/8570a23843b3/fimmu-08-01865-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/c750edc9e6f8/fimmu-08-01865-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/b8ac1cf55688/fimmu-08-01865-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/0245b98ad2ee/fimmu-08-01865-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/d362478ab12e/fimmu-08-01865-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/e85db4f91f19/fimmu-08-01865-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/8570a23843b3/fimmu-08-01865-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/c750edc9e6f8/fimmu-08-01865-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1dd/5742589/b8ac1cf55688/fimmu-08-01865-g006.jpg

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