| Literature DB >> 35842561 |
Timothy C Borbet1, Miranda B Pawline1, Xiaozhou Zhang2, Matthew F Wipperman3,4, Sebastian Reuter5, Timothy Maher1, Jackie Li1, Tadasu Iizumi1,6, Zhan Gao6, Megan Daniele1,7, Christian Taube5, Sergei B Koralov1, Anne Müller8, Martin J Blaser9.
Abstract
Antibiotics, among the most used medications in children, affect gut microbiome communities and metabolic functions. These changes in microbiota structure can impact host immunity. We hypothesized that early-life microbiome alterations would lead to increased susceptibility to allergy and asthma. To test this, mouse pups between postnatal days 5-9 were orally exposed to water (control) or to therapeutic doses of azithromycin or amoxicillin. Later in life, these mice were sensitized and challenged with a model allergen, house dust mite (HDM), or saline. Mice with early-life azithromycin exposure that were challenged with HDM had increased IgE and IL-13 production by CD4+ T cells compared to unexposed mice; early-life amoxicillin exposure led to fewer abnormalities. To test that the microbiota contained the immunological cues to alter IgE and cytokine production after HDM challenge, germ-free mice were gavaged with fecal samples of the antibiotic-perturbed microbiota. Gavage of adult germ-free mice did not result in altered HDM responses, however, their offspring, which acquired the antibiotic-perturbed microbiota at birth showed elevated IgE levels and CD4+ cytokines in response to HDM, and altered airway reactivity. These studies indicate that early-life microbiota composition can heighten allergen-driven Th2/Th17 immune pathways and airway responses in an age-dependent manner.Entities:
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Year: 2022 PMID: 35842561 DOI: 10.1038/s41385-022-00544-5
Source DB: PubMed Journal: Mucosal Immunol ISSN: 1933-0219 Impact factor: 8.701