Article

Modeling cell-cell interactions to advance drug discovery in Idiopathic Pulmonary Fibrosis

2026-02-02

Abstract excerpt

<h4>Background</h4> Idiopathic Pulmonary Fibrosis (IPF) is characterized by scarring and remodeling of lung tissue, leading to progressive pulmonary dysfunction. Currently, very little is known about the steps involved in disease initiation and progression because models of IPF poorly replicate these processes. However, understanding the pathogenesis of IPF is essential for developing effective therapies. To addr...

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Literature Corpus work: 65199aab-fc1f-53fb-a96c-02f8bf9939ee
DOI: 10.64898/2026.01.29.702646

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