Department of Pathology, New York University School of Medicine, New York, NY, USA.
Institute of Molecular Cancer Research, University of Zurich, Zurich, Switzerland.
Mucosal Immunol. 2022 May;15(5):1000-1011. doi: 10.1038/s41385-022-00544-5. Epub 2022 Jul 16.
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.
抗生素是儿童最常使用的药物之一,会影响肠道微生物组群落和代谢功能。这些微生物群落结构的变化可能会影响宿主的免疫功能。我们假设,生命早期的微生物群落改变会导致过敏和哮喘的易感性增加。为了验证这一点,我们在出生后 5-9 天的小鼠幼崽中经口给予水(对照)或治疗剂量的阿奇霉素或阿莫西林。在生命后期,这些小鼠被致敏并接受屋尘螨(HDM)或生理盐水的挑战。与未暴露的小鼠相比,早期接受阿奇霉素暴露的小鼠在接受 HDM 挑战后,CD4 T 细胞产生的 IgE 和 IL-13 增加;早期接受阿莫西林暴露的小鼠则没有出现这些异常。为了验证微生物群包含改变 HDM 挑战后 IgE 和细胞因子产生的免疫线索,我们用抗生素扰乱的微生物群的粪便样本灌胃无菌小鼠。给成年无菌小鼠灌胃不会导致 HDM 反应改变,但是它们的后代在出生时就获得了抗生素扰乱的微生物群,这些后代对 HDM 表现出更高的 IgE 水平和 CD4 细胞因子水平,以及改变的气道反应性。这些研究表明,生命早期的微生物群落组成可以以年龄依赖的方式增强过敏原驱动的 Th2/Th17 免疫途径和气道反应。