作者
Thomas Hagan,Mario Cortese,Nadine Rouphael,Carolyn M. Boudreau,Caitlin Linde,Mohan S. Maddur,Jishnu Das,Hong Wang,Jenna J. Guthmiller,Nai‐Ying Zheng,Min Huang,Amit A. Uphadhyay,Luiz Gustavo Gardinassi,Caroline Petitdemange,Michele Paine McCullough,Sara J. Johnson,Kiran Gill,Barbara Cervasi,Jun Zou,Alexis Bretin,Megan Hahn,Andrew T. Gewirtz,Steve Bosinger,Patrick C. Wilson,Shuzhao Li,Galit Alter,Surender Khurana,Hana Golding,Bali Pulendran
摘要
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.