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Host-microbial interactions at the nasal mucosa in young children and adults: A retrospective, cross-sectional study

  • Jesús Reiné
  • , Lisa A. King
  • , Youvika Singh
  • , Wouter A.A. de Steenhuijsen Piters
  • , Beatriz F. Carniel
  • , Carla Solórzano
  • , Elena Mitsi
  • , Sherin Pojar
  • , Elissavet Nikolaou
  • , Esther L. German
  • , Annie Blizard
  • , Fernando Marcon
  • , Alexandre H.C. Marques
  • , Astrid L. Voskamp
  • , Mei Ling Chu
  • , Raiza Hasrat
  • , Helen Hill
  • , Caz Hales
  • , Lynsey Brown
  • , Victoria Horsley
  • Lisa P. Hughes, Seher R. Zaidi, Victoria Connor, Ben Morton, Andrea M. Collins, Jamie Rylance, Hugh Adler, Hermelijn H. Smits, Ahmed Mahfouz, Paul S. McNamara, Helder I. Nakaya, Debby Bogaert, Daniela M. Ferreira, Simon P. Jochems
  • University of Oxford
  • Leiden University
  • Utrecht University
  • National Institute of Public Health and the Environment
  • Liverpool School of Tropical Medicine
  • Murdoch Children's Research Institute
  • University of Melbourne
  • London School of Hygiene and Tropical Medicine
  • Liverpool University Hospitals NHS Foundation Trust
  • Alder Hey Children's NHS Foundation Trust
  • Malawi-Liverpool-Wellcome Trust Clinical Research Programme
  • Delft University of Technology
  • Universidade de São Paulo
  • Hospital Israelita Albert Einstein
  • University of Edinburgh

Research output: Contribution to journalArticlepeer-review

Abstract

Young children are at increased risk for respiratory tract infections and are frequently colonized by respiratory pathogens. However, how the mucosal immune system differs between children and adults is relatively unknown. We collected nasal samples from 50 young children (aged 1–5 years) and 318 young adults (aged 18–34 years) to study how the mucosal immune system and host-microbe interactions differ with age. We used multi-omics data integration to combine host (immunophenotyping, transcriptomic, and cytokines) and microbial (16S-rRNA amplicon sequencing, viral PCRs, and pneumococcal culture) datasets. Young children had a paucity of mucosal granulocytes, while B and T cell subsets were increased. Children also had increased immune activation and inflammation, which associated with the presence of Haemophilus spp. and pneumococcus, but not viruses. In adults, Haemophilus spp. associated with T cell and monocyte recruitment, while Dolosigranulum negatively associated with neutrophil degranulation. Thus, nasal immune composition and host-pathogen interactions were clearly age dependent.

Original languageEnglish
Article number117346
JournalCell Reports
Volume45
Issue number5
DOIs
Publication statusPublished - 22 May 2026

Keywords

  • aging
  • host-pathogen interactions
  • microbiome
  • mucosal immune system
  • nasal samples
  • upper respiratory tract immunity
  • young adults
  • young children

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