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  2. Early-life antibiotic dysbiosis impairs microbial tryptophan- nicotinic acid metabolism exacerbating food allergy in adulthood

Early-life antibiotic dysbiosis impairs microbial tryptophan- nicotinic acid metabolism exacerbating food allergy in adulthood

  • Int Immunopharmacol. 2025 Jun 26:159:114888. doi: 10.1016/j.intimp.2025.114888.
Lei Wang 1 Chuqiao Lai 1 Jiahui Yu 1 Xinyi Xu 1 Minghui Jia 2 Zheng Wang 1 Yeqing Chen 1 Qianjin Lou 1 Qihong Tao 3 Hao Hu 3 Zhanqing Fu 3 Xiaoxiao Jia 1 Weixi Zhang 4
Affiliations

Affiliations

  • 1 Department of Pediatric Allergy and Immunology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou City 325000, China.
  • 2 Zhejiang Chinese Medical University, Hangzhou City 310053, China.
  • 3 Wenzhou Medical University, Wenzhou City 325000, China.
  • 4 Department of Pediatric Allergy and Immunology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou City 325000, China. Electronic address: zhangweixi112@163.com.
Abstract

Food allergy (FA) pathogenesis links to intestinal dysbiosis, with Antibiotic exposure a suspected risk factor, yet mechanisms are unclear. Our study shows early life (EL) Antibiotic exposure in mice heightens susceptibility to OVA - induced allergic intestinal inflammation. EL - Antibiotics cause intestinal dysbiosis, like Clostridia and Muribaculaceae depletion and Sutterellaceae enrichment, disrupting tryptophan metabolism and reducing nicotinic acid (NA). NA deficiency impairs gut barrier and Th2/Treg balance. However, NA supplementation restores these via GPR109A. In human pediatric cohorts, food - allergic children with EL - Antibiotic exposure have lower gut NA levels. We integrated mouse and human data with multi - omics, revealing EL - Abx regulates FA through the "microbiota - metabolism - immunity" axis, and suggest targeting NA pathway to counter Antibiotic - related FA risk.

Keywords

Early life antibiotic exposure; Food allergy; Gut microbiome; Nicotinic acid; Prospective pediatric cohorts; Tryptophan metabolism.

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