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早期生活中的抗生素驱动的菌群失调会破坏色氨酸-3-丙酸的产生,并加重成年期的过敏性气道炎症。

Antibiotic-driven dysbiosis in early life disrupts indole-3-propionic acid production and exacerbates allergic airway inflammation in adulthood.

机构信息

Department of Immunology, Mucosal Immunology Research Group, School of Translational Medicine, Monash University, Melbourne, VIC, Australia.

Department of Immunology, Mucosal Immunology Research Group, School of Translational Medicine, Monash University, Melbourne, VIC, Australia.

出版信息

Immunity. 2024 Aug 13;57(8):1939-1954.e7. doi: 10.1016/j.immuni.2024.06.010. Epub 2024 Jul 15.

DOI:10.1016/j.immuni.2024.06.010
PMID:39013465
Abstract

Antibiotic use in early life disrupts microbial colonization and increases the risk of developing allergies and asthma. We report that mice given antibiotics in early life (EL-Abx), but not in adulthood, were more susceptible to house dust mite (HDM)-induced allergic airway inflammation. This susceptibility was maintained even after normalization of the gut microbiome. EL-Abx decreased systemic levels of indole-3-propionic acid (IPA), which induced long-term changes to cellular stress, metabolism, and mitochondrial respiration in the lung epithelium. IPA reduced mitochondrial respiration and superoxide production and altered chemokine and cytokine production. Consequently, early-life IPA supplementation protected EL-Abx mice against exacerbated HDM-induced allergic airway inflammation in adulthood. These results reveal a mechanism through which EL-Abx can predispose the lung to allergic airway inflammation and highlight a possible preventative approach to mitigate the detrimental consequences of EL-Abx.

摘要

早期生活中使用抗生素会破坏微生物定植,并增加患过敏和哮喘的风险。我们报告称,早期(EL-Abx)而非成年期使用抗生素的小鼠更容易发生屋尘螨(HDM)诱导的过敏性气道炎症。即使肠道微生物组恢复正常,这种易感性仍得以维持。EL-Abx 降低了系统性吲哚-3-丙酸(IPA)水平,IPA 会导致肺上皮细胞的长期细胞应激、代谢和线粒体呼吸改变。IPA 降低了线粒体呼吸和超氧化物的产生,并改变了趋化因子和细胞因子的产生。因此,早期生活 IPA 补充剂可保护 EL-Abx 小鼠免受成年后 HDM 诱导的过敏性气道炎症的加重。这些结果揭示了 EL-Abx 使肺部易患过敏性气道炎症的一种机制,并强调了一种可能的预防措施来减轻 EL-Abx 的有害后果。

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