Early-Life Antibiotic-Driven Dysbiosis Leads to Dysregulated Vaccine Immune Responses in Mice

Cell Host Microbe. 2018 May 9;23(5):653-660.e5. doi: 10.1016/j.chom.2018.04.009.

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.

Keywords: CD4(+) T cells; antibiotics; antibody response; early-life; microbiota; vaccines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / adverse effects*
  • Anti-Bacterial Agents / immunology*
  • Anti-Bacterial Agents / therapeutic use
  • Antibody Formation / immunology*
  • CD4-Positive T-Lymphocytes / immunology
  • Cytokines / metabolism
  • DNA, Bacterial
  • Dysbiosis / immunology*
  • Feces / microbiology
  • Female
  • Gastrointestinal Microbiome / drug effects
  • Gastrointestinal Microbiome / genetics
  • Gastrointestinal Microbiome / immunology
  • Mice
  • Mice, Inbred C57BL
  • Models, Animal
  • Pregnancy
  • RNA, Ribosomal, 16S / genetics
  • Vaccination
  • Vaccines / immunology*

Substances

  • Anti-Bacterial Agents
  • Cytokines
  • DNA, Bacterial
  • RNA, Ribosomal, 16S
  • Vaccines