Longitudinal profiling of the intestinal microbiome in children with cystic fibrosis treated with elexacaftor-tezacaftor-ivacaftor.

CFTR modulator antibiotic resistance cystic fibrosis elexacaftor intestinal inflammation ivacaftor metagenomic sequencing microbiome pediatric tezacaftor

Journal

mBio
ISSN: 2150-7511
Titre abrégé: mBio
Pays: United States
ID NLM: 101519231

Informations de publication

Date de publication:
26 Jan 2024
Historique:
medline: 26 1 2024
pubmed: 26 1 2024
entrez: 26 1 2024
Statut: aheadofprint

Résumé

The intestinal microbiome influences growth and disease progression in children with cystic fibrosis (CF). Elexacaftor-tezacaftor-ivacaftor (ELX/TEZ/IVA), the newest pharmaceutical modulator for CF, restores the function of the pathogenic mutated CF transmembrane conductance regulator (CFTR) channel. We performed a single-center longitudinal analysis of the effect of ELX/TEZ/IVA on the intestinal microbiome, intestinal inflammation, and clinical parameters in children with CF. Following ELX/TEZ/IVA, children with CF had significant improvements in body mass index and percent predicted forced expiratory volume in one second, and required fewer antibiotics for respiratory infections. Intestinal microbiome diversity increased following ELX/TEZ/IVA coupled with a decrease in the intestinal carriage of

Identifiants

pubmed: 38275294
doi: 10.1128/mbio.01935-23
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0193523

Auteurs

Seth A Reasoner (SA)

Department of Pathology, Microbiology, and Immunology, Division of Molecular Pathogenesis, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Rachel Bernard (R)

Department of Pediatrics, Division of Gastroenterology, Hepatology, and Nutrition, Monroe Carrell Junior Children's Hospital at Vanderbilt, Nashville, Tennessee, USA.

Adam Waalkes (A)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.

Kelsi Penewit (K)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.

Janessa Lewis (J)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.

Andrew G Sokolow (AG)

Department of Pediatrics, Division of Allergy, Immunology, and Pulmonary Medicine, Monroe Carrell Junior Children's Hospital at Vanderbilt, Nashville, Tennessee, USA.

Rebekah F Brown (RF)

Department of Pediatrics, Division of Allergy, Immunology, and Pulmonary Medicine, Monroe Carrell Junior Children's Hospital at Vanderbilt, Nashville, Tennessee, USA.

Kathryn M Edwards (KM)

Department of Pediatrics, Division of Infectious Diseases, Monroe Carrell Junior Children's Hospital at Vanderbilt, Nashville, Tennessee, USA.

Stephen J Salipante (SJ)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.

Maria Hadjifrangiskou (M)

Department of Pathology, Microbiology, and Immunology, Division of Molecular Pathogenesis, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Center for Personalized Microbiology (CPMi), Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Vanderbilt Institute for Infection, Immunology and Inflammation, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Maribeth R Nicholson (MR)

Department of Pediatrics, Division of Gastroenterology, Hepatology, and Nutrition, Monroe Carrell Junior Children's Hospital at Vanderbilt, Nashville, Tennessee, USA.
Vanderbilt Institute for Infection, Immunology and Inflammation, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Classifications MeSH