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