免疫学
微生物群
免疫系统
免疫球蛋白E
肠道菌群
过敏
生物
过敏原
抗生素
免疫
屋尘螨
后代
医学
作者
Timothy C. Borbet,Miranda B. Pawline,Xiaozhou Zhang,Matthew F. Wipperman,Sebastian Reuter,Timothy Maher,Jackie Li,Tadasu Iizumi,Zhan Gao,Megan Daniele,Christian Taube,Sergei B. Koralov,Anne Müller,Martin J. Blaser
标识
DOI:10.1038/s41385-022-00544-5
摘要
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.
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