Interstitial lung diseases

M Wijsenbeek, A Suzuki, TM Maher - The Lancet, 2022 - thelancet.com
Over 200 interstitial lung diseases, from ultra rare to relatively common, are recognised.
Most interstitial lung diseases are characterised by inflammation or fibrosis within the …

[HTML][HTML] The lung microbiome: progress and promise

SA Whiteside, JE McGinniss… - The Journal of Clinical …, 2021 - Am Soc Clin Investig
The healthy lung was long thought of as sterile, but recent advances using molecular
sequencing approaches have detected bacteria at low levels. Healthy lung bacteria largely …

Respiratory microbiome and epithelial interactions shape immunity in the lungs

R Invernizzi, CM Lloyd, PL Molyneaux - Immunology, 2020 - Wiley Online Library
The airway epithelium represents a physical barrier to the external environment acting as
the first line of defence against potentially harmful environmental stimuli including microbes …

The interplay of the genetic architecture, aging, and environmental factors in the pathogenesis of idiopathic pulmonary fibrosis

A Pardo, M Selman - American journal of respiratory cell and …, 2021 - atsjournals.org
Idiopathic pulmonary fibrosis (IPF) is a chronic fibrosing lung disease of indeterminate
etiology and limited therapeutic options. The initiation, development, and progression of IPF …

Lung microbiota predict chronic rejection in healthy lung transplant recipients: a prospective cohort study

MP Combs, DS Wheeler, JE Luth… - The Lancet …, 2021 - thelancet.com
Background Alterations in the respiratory microbiome are common in chronic lung diseases,
correlate with decreased lung function, and have been associated with disease progression …

Therapeutic targeting of the respiratory microbiome

SH Chotirmall, D Bogaert, JD Chalmers… - American journal of …, 2022 - atsjournals.org
Culture-independent microbiology has transformed our understanding of the respiratory
microbiome in health and disease (1). Enabled by advances in next-generation sequencing …

[HTML][HTML] Enhanced IL-1β release following NLRP3 and AIM2 inflammasome stimulation is linked to mtROS in airway macrophages in pulmonary fibrosis

A Trachalaki, E Tsitoura, S Mastrodimou… - Frontiers in …, 2021 - frontiersin.org
Fibrotic Interstitial lung diseases (ILDs) are complex disorders of variable clinical behaviour.
The majority of them cause significant morbidity, whilst Idiopathic Pulmonary Fibrosis (IPF) is …

The respiratory microbiome in chronic hypersensitivity pneumonitis is distinct from that of idiopathic pulmonary fibrosis

R Invernizzi, BG Wu, J Barnett, P Ghai… - American journal of …, 2021 - atsjournals.org
Rationale: Chronic hypersensitivity pneumonitis (CHP) is a condition that arises after
repeated exposure and sensitization to inhaled antigens. The lung microbiome is …

Effect of co-trimoxazole (trimethoprim-sulfamethoxazole) vs placebo on death, lung transplant, or hospital admission in patients with moderate and severe idiopathic …

AM Wilson, AB Clark, T Cahn, ER Chilvers, W Fraser… - Jama, 2020 - jamanetwork.com
Importance Idiopathic pulmonary fibrosis (IPF) has a poor prognosis and limited treatment
options. Patients with IPF have altered lung microbiota, with bacterial burden within the …

Genetic risk factors for idiopathic pulmonary fibrosis: insights into immunopathogenesis

JE Michalski, DA Schwartz - Journal of Inflammation Research, 2021 - Taylor & Francis
Idiopathic pulmonary fibrosis is an etiologically complex interstitial lung disease
characterized by progressive scarring of the lungs with a subsequent decline in lung …