Christina Grosserichter-Wagener, Kirsten I M Looman, Sanne A Beth, Djawad Radjabzadeh, Paul A Gill, Kyra N Smit, Liesbeth Duijts, Jessica C Kiefte-de Jong, Robert Kraaij, Henriëtte A Moll, Menno C van Zelm
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引用次数: 0
Abstract
Objective: Studies in mouse models and human adults have shown that the intestinal microbiota composition can affect peripheral immune cells. We here examined whether the gut microbiota compositions affect B and T-cell subsets in children.
Methods: The intestinal microbiota was characterized from stool samples of 344 10-year-old children from the Generation R Study by performing 16S rRNA sequencing. Bray-Curtis dissimilarity was used to cluster distinct microbiome compositions (enterotypes). B-cell and T-cell phenotypes were defined by 11-color-flow cytometry. Linear regression models with adjustment for lifestyle and child characteristics were performed to determine associations between enterotypes and immune cell numbers.
Results: Three enterotypes with distinct microbiota composition were found, characterized by high abundance of Prevotella, Bacteroides and Blautia. Children with the Blautia enterotype had decreased numbers of plasmablasts, CD4+ central memory (Tcm) T cells and follicular T-helper cells (Tfh), while Th22 cells and CD4+ effector memory (Tem) T cells, CD27-IgA+ memory B cells and CD27-IgE+ memory B cells, were increased in these children. In addition, in children with the Blautia enterotype CD4+ Tcm cell numbers expressing the β7 integrin, which can pair with α4 to mediate intestinal homing were also lower, while CD4+β7+ Tem cell numbers were higher than in the other enterotypes.
Conclusion: The Blautia enterotype showed features beneficial for human health. Enterotypes were associated with differences in memory B- and T-cell compartments. This study is unique in the detailed analysis of the B and T-cell compartment and the intestinal microbiome in a large generic pediatric cohort, enabling correction for child and maternal covariates. These outcomes could guide further studies about the impact of intestinal microbiome intervention, for instance through diet and microbiota metabolites such as short chain fatty acid production.
目的:对小鼠模型和人类成年人的研究表明,肠道微生物群的组成可影响外周免疫细胞。我们在此研究了肠道微生物群的组成是否会影响儿童的 B 细胞和 T 细胞亚群:方法:通过 16S rRNA 测序,对 344 名来自 R 世代研究(Generation R Study)的 10 岁儿童的粪便样本进行了肠道微生物群特征描述。利用布雷-柯蒂斯相似度对不同的微生物群组成(肠型)进行聚类。B 细胞和 T 细胞表型由 11 色流式细胞术确定。通过调整生活方式和儿童特征的线性回归模型来确定肠型与免疫细胞数量之间的关系:结果:发现了三种具有不同微生物群组成的肠型,其特点是普雷沃特氏菌(Prevotella)、巴氏杆菌(Bacteroides)和布劳特氏菌(Blautia)含量较高。布劳氏菌肠型儿童的浆细胞、CD4+中央记忆(Tcm)T细胞和滤泡T辅助细胞(Tfh)数量减少,而Th22细胞、CD4+效应记忆(Tem)T细胞、CD27-IgA+记忆B细胞和CD27-IgE+记忆B细胞数量增加。此外,在布劳提亚肠型儿童中,表达β7整合素(可与α4配对介导肠道)的CD4+Tcm细胞数量也较低,而CD4+β7+Tem细胞数量则高于其他肠型:结论:布劳蒂亚肠型显示出有益于人类健康的特征。肠型与记忆 B 细胞和 T 细胞区系的差异有关。这项研究的独特之处在于,它详细分析了大型通用儿科队列中的 B 细胞和 T 细胞群以及肠道微生物群,并对儿童和母亲的协变量进行了校正。这些结果可指导有关肠道微生物群干预影响的进一步研究,例如通过饮食和微生物群代谢物(如短链脂肪酸的产生)进行干预。
期刊介绍:
Clinical Immunology publishes original research delving into the molecular and cellular foundations of immunological diseases. Additionally, the journal includes reviews covering timely subjects in basic immunology, along with case reports and letters to the editor.