In the recent years, extracellular vesicles (EVs) drew a growing interest in scientific
community, especially for their intrinsic role of cell-cell communication entities between local …

In the longtime challenge of identifying specific, easily detectable and reliable biomarkers of
IPF, BALF proteomics is providing interesting new insights into its pathogenesis. To the best …

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, irreversible, and highly fatal
disease. It is characterized by the increased activation of both fibroblast and myofibroblast …

Background Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial pneumonia of
unknown etiology often leading to respiratory failure. Over half of IPF patients present with …

High‐resolution computed tomography (HRCT) imaging is critical for diagnostic evaluation
of Idiopathic Pulmonary Fibrosis (IPF). However, several other interstitial lung diseases …

Background Inflammatory respiratory diseases, such as interstitial lung disease (ILD),
bronchial asthma (BA), chronic obstructive pulmonary disease (COPD), and respiratory …

Idiopathic pulmonary fibrosis (IPF) is a lethal and chronic lung disease characterized by
aberrant intercellular communication, increased extracellular matrix (ECM) deposition, and …

Diagnosis of interstitial lung diseases (ILD) is difficult to perform. Extracellular vesicles (EVs)
facilitate cell-to-cell communication, and they are released by a variety of cells. Our goal …

Introduction: Interstitial lung diseases (ILDs) are a heterogeneous group of diffuse
parenchymal lung disorders characterized by the pathogenetic involvement of interstitium …

Diagnosis of interstitial lung diseases (ILD) is difficult to perform. Extracellular vesicles (EVs)
facilitate cell-to-cell communication. Our goal aimed to investigate EVs markers in …