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Description
[25], Cenigaonandia-Campillo et al

Idiopathic Pulmonary Fibrosis (IPF) IPF is a fatal and irreversible interstitial lung disease characterized by the involvement of ROSs in specific fibrotic processes, including macrophage polarization, immunosenescence, alveolar epithelial cell apoptosis, myofibroblast differentiation, and alterations in the acellular extracellular matrix [101]

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