| Literature DB >> 29746836 |
Miriam Anne Lynn1, Damon John Tumes2, Jocelyn Mei Choo3, Anastasia Sribnaia1, Stephen James Blake1, Lex Ee Xiang Leong3, Graeme Paul Young4, Helen Siobhan Marshall5, Steve Lodewijk Wesselingh3, Geraint Berian Rogers3, David John Lynn6.
Abstract
Antibody-mediated responses play a critical role in vaccine-mediated immunity. However, for reasons that are poorly understood, these responses are highly variable between individuals. Using a mouse model, we report that antibiotic-driven intestinal dysbiosis, specifically in early life, leads to significantly impaired antibody responses to five different adjuvanted and live vaccines. Restoration of the commensal microbiota following antibiotic exposure rescues these impaired responses. In contrast, antibiotic-treated adult mice do not exhibit impaired antibody responses to vaccination. Interestingly, in contrast to impaired antibody responses, immunized mice exposed to early-life antibiotics display significantly enhanced T cell cytokine recall responses upon ex vivo restimulation with the vaccine antigen. Our results demonstrate that, in mice, antibiotic-driven dysregulation of the gut microbiota in early life can modulate immune responses to vaccines that are routinely administered to infants worldwide.Entities:
Keywords: CD4(+) T cells; antibiotics; antibody response; early-life; microbiota; vaccines
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Year: 2018 PMID: 29746836 DOI: 10.1016/j.chom.2018.04.009
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023