Citation

BibTex format

@article{Mac:2024:10.1183/16000617.0038-2024,
author = {Mac, Aogáin M and Dicker, AJ and Mertsch, P and Chotirmall, SH},
doi = {10.1183/16000617.0038-2024},
journal = {Eur Respir Rev},
title = {Infection and the microbiome in bronchiectasis.},
url = {http://dx.doi.org/10.1183/16000617.0038-2024},
volume = {33},
year = {2024}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Bronchiectasis is marked by bronchial dilatation, recurrent infections and significant morbidity, underpinned by a complex interplay between microbial dysbiosis and immune dysregulation. The identification of distinct endophenotypes have refined our understanding of its pathogenesis, including its heterogeneous disease mechanisms that influence treatment and prognosis responses. Next-generation sequencing (NGS) has revolutionised the way we view airway microbiology, allowing insights into the "unculturable". Understanding the bronchiectasis microbiome through targeted amplicon sequencing and/or shotgun metagenomics has provided key information on the interplay of the microbiome and host immunity, a central feature of disease progression. The rapid increase in translational and clinical studies in bronchiectasis now provides scope for the application of precision medicine and a better understanding of the efficacy of interventions aimed at restoring microbial balance and/or modulating immune responses. Holistic integration of these insights is driving an evolving paradigm shift in our understanding of bronchiectasis, which includes the critical role of the microbiome and its unique interplay with clinical, inflammatory, immunological and metabolic factors. Here, we review the current state of infection and the microbiome in bronchiectasis and provide views on the future directions in this field.
AU - Mac,Aogáin M
AU - Dicker,AJ
AU - Mertsch,P
AU - Chotirmall,SH
DO - 10.1183/16000617.0038-2024
PY - 2024///
TI - Infection and the microbiome in bronchiectasis.
T2 - Eur Respir Rev
UR - http://dx.doi.org/10.1183/16000617.0038-2024
UR - https://www.ncbi.nlm.nih.gov/pubmed/38960615
VL - 33
ER -

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