# Datasets of 16S rRNA gene amplicon sequences, metabolites, and soluble immune components in bronchoalveolar lavage samples from severe asthmatic and age-matched control children

**Authors:** Mélanie Briard, Blanche Guillon, Eric Venot, Marta Grauso, Aurélia Bruneau, Marie-Noëlle Rossignol, François Fenaille, Florence Castelli, Muriel Thomas, Guillaume Lezmi, Maria Leite-de-Moraes, Karine Adel-Patient, Vinciane Saint-Criq

PMC · DOI: 10.1016/j.dib.2025.112359 · Data in Brief · 2025-12-07

## TL;DR

This paper provides datasets from bronchoalveolar lavage samples of children with severe asthma and controls, including microbiota, metabolites, and immune components for further research.

## Contribution

The study introduces comprehensive multi-omics datasets from children with severe asthma and age-matched controls for investigating disease mechanisms and biomarkers.

## Key findings

- Datasets include microbiota profiles, metabolites, and immune components from BAL samples of children with severe asthma and controls.
- The data are publicly available for reuse in multi-omics analyses and comparisons with other cohorts.
- The resources aim to identify local biomarkers and mechanisms underlying severe asthma endotypes.

## Abstract

Severe asthma (SA) is a heterogeneous condition characterized by multiple phenotypes, each characterized by different endotypes. Understanding the mechanisms occurring in the lungs of children with SA can help in understanding pathogenesis and in providing the most effective therapeutic strategies. This article describes microbiota, metabolites, and soluble immune components assessed in bronchoalveolar lavage (BAL) fluids from children with severe asthma (n = 20) and age-matched disease controls (n = 10). The article includes: (i) the protocol used to process BAL samples for 16S rRNA gene amplicon sequencing, metabolomic profiling and immune components assays; (ii) the bioinformatics steps applied to 16S rRNA and metabolomics dataset; (iii) an overview of the raw 16S rRNA gene amplicon sequencing data, presented as ASV and affiliation tables, raw data from untargeted metabolomics and the abundances of each of the eighty eight metabolites annotated with the highest confidence level, and concentrations of seventy three cytokines and of total IgG, IgA and IgE. Each dataset is available in the INRAE data repository (https://entrepot.recherche.data.gouv.fr/dataverse/inrae) with respective DOI: MICROBIOTA: 10.57745/LL3TFW, METABOLITES: 10.57745/1L8VRI, IMMUNE COMPONENTS: 10.57745/JOOGRQ

These datasets provide valuable resources for further investigating the molecular mechanisms underlying severe asthma in children and its trajectories. They also offer the potential to identify a local signature of severe asthma through complementary multi-omics analyses and to discover local biomarkers associated with asthma endotypes. Datasets can also be reused to compare with other cohorts (children or adults) or to serve as reference datasets for other pulmonary diseases.

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}
- **Diseases:** asthma (MESH:D001249), asthmatic (MESH:D013224), pulmonary diseases (MESH:D008171), SA (MESH:D045169)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12769396/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12769396/full.md

## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12769396/full.md

---
Source: https://tomesphere.com/paper/PMC12769396