| Literature DB >> 30092197 |
Vanessa C Harris1, Bastiaan W Haak2, Scott A Handley3, Baoming Jiang4, Daniel E Velasquez4, Barry L Hykes3, Lindsay Droit3, Guy A M Berbers5, Elles Marleen Kemper6, Ester M M van Leeuwen7, Michael Boele van Hensbroek8, Willem Joost Wiersinga2.
Abstract
Rotavirus vaccines (RVV) protect against childhood gastroenteritis caused by rotavirus (RV) but have decreased effectiveness in low- and middle-income settings. This proof-of-concept, randomized-controlled, open-label trial tested if microbiome modulation can improve RVV immunogenicity. Healthy adults were randomized and administered broad-spectrum (oral vancomycin, ciprofloxacin, metronidazole), narrow-spectrum (vancomycin), or no antibiotics and then vaccinated with RVV, 21 per group per protocol. Baseline anti-RV IgA was high in all subjects. Although antibiotics did not alter absolute anti-RV IgA titers, RVV immunogenicity was boosted at 7 days in the narrow-spectrum group. Further, antibiotics increased fecal shedding of RV while also rapidly altering gut bacterial beta diversity. Beta diversity associated with RVV immunogenicity boosting at day 7 and specific bacterial taxa that distinguish RVV boosters and RV shedders were identified. Despite the negative primary endpoint, this study demonstrates that microbiota modification alters the immune response to RVV and supports further exploration of microbiome manipulation to improve RVV immunogenicity.Entities:
Keywords: Bacteroidetes; Firmicutes; Proteobacteria; anti-IgA; ciprofloxacin; gastroenteritis; gastrointestinal microbiome; immunoglobulin A; metronidazole; microbiota; oral vaccines; rotavirus; rotavirus infections; rotavirus vaccines; vaccines; vancomycin
Mesh:
Substances:
Year: 2018 PMID: 30092197 DOI: 10.1016/j.chom.2018.07.005
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023