z-logo
open-access-imgOpen Access
Antibiotics-Driven Gut Microbiome Perturbation Alters Immunity to Vaccines in Humans
Author(s) -
Thomas Hagan,
Mario Cortese,
Nadine Rouphael,
Carolyn M. Boudreau,
Caitlin Linde,
Mohan S. Maddur,
Jishnu Das,
Hong Wang,
Jenna J. Guthmiller,
NaiYing 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
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.08.010
Subject(s) - biology , immunity , microbiome , antibiotics , inflammasome , immunology , antibody , vaccination , immune system , microbiology and biotechnology , inflammation , bioinformatics
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom