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抗生素驱动的肠道微生物组扰动改变了人类对疫苗的免疫反应。

Antibiotics-Driven Gut Microbiome Perturbation Alters Immunity to Vaccines in Humans.

机构信息

Institute for Immunity, Transplantation and Infection, School of Medicine, Stanford University, Stanford, CA 94305, USA.

Hope Clinic of the Emory Vaccine Center, Decatur, GA 30030, USA.

出版信息

Cell. 2019 Sep 5;178(6):1313-1328.e13. doi: 10.1016/j.cell.2019.08.010.

Abstract

Emerging evidence indicates a central role for the microbiome in immunity. However, causal evidence in humans is sparse. Here, we administered broad-spectrum antibiotics to healthy adults prior and subsequent to seasonal influenza vaccination. Despite a 10,000-fold reduction in gut bacterial load and long-lasting diminution in bacterial diversity, antibody responses were not significantly affected. However, in a second trial of subjects with low pre-existing antibody titers, there was significant impairment in H1N1-specific neutralization and binding IgG1 and IgA responses. In addition, in both studies antibiotics treatment resulted in (1) enhanced inflammatory signatures (including AP-1/NR4A expression), observed previously in the elderly, and increased dendritic cell activation; (2) divergent metabolic trajectories, with a 1,000-fold reduction in serum secondary bile acids, which was highly correlated with AP-1/NR4A signaling and inflammasome activation. Multi-omics integration revealed significant associations between bacterial species and metabolic phenotypes, highlighting a key role for the microbiome in modulating human immunity.

摘要

新出现的证据表明,微生物组在免疫中起着核心作用。然而,人类中因果关系的证据很少。在这里,我们在季节性流感疫苗接种前后给健康成年人服用广谱抗生素。尽管肠道细菌负荷减少了 10,000 倍,细菌多样性也长期减少,但抗体反应并没有受到显著影响。然而,在第二项针对低预先存在抗体滴度的受试者的试验中,H1N1 特异性中和以及结合 IgG1 和 IgA 反应显著受损。此外,在这两项研究中,抗生素治疗导致了(1)炎症特征的增强(包括 AP-1/NR4A 表达),这在老年人中观察到,以及树突状细胞的激活增加;(2)代谢轨迹的不同,血清次级胆汁酸减少了 1000 倍,这与 AP-1/NR4A 信号和炎症小体激活高度相关。多组学整合揭示了细菌种类和代谢表型之间的显著关联,突出了微生物组在调节人类免疫中的关键作用。

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