New therapeutics based on emerging concepts in pulmonary fibrosis

• Published in: Expert opinion on therapeutic targets Vol. 23; no. 1; p. 69
• Main Authors: Sontake, Vishwaraj, Gajjala, Prathibha R, Kasam, Rajesh K, Madala, Satish K
• Format: Journal Article
• Language: English
• Published: England 02-01-2019
• Subjects: Animals; Cell Proliferation - physiology; Disease Progression; Extracellular Matrix - metabolism; Fibroblasts - cytology; Humans; Idiopathic Pulmonary Fibrosis - mortality; Idiopathic Pulmonary Fibrosis - physiopathology; Idiopathic Pulmonary Fibrosis - therapy; Lung - physiopathology; Molecular Targeted Therapy; Myofibroblasts - cytology; Survival; Wilms’ tumor1; lung; idiopathic pulmonary fibrosis; myofibroblasts; Heat shock protein 90
• ISSN: 1744-7631
• DOI: 10.1080/14728222.2019.1552262

Fibrosis is an irreversible pathological endpoint in many chronic diseases, including pulmonary fibrosis. Idiopathic pulmonary fibrosis (IPF) is a progressive and often fatal condition characterized by (myo)fibroblast proliferation and transformation in the lung, expansion of the extracellular matrix, and extensive remodeling of the lung parenchyma. Recent evidence indicates that IPF prevalence and mortality rates are growing in the United States and elsewhere. Despite decades of research on the pathogenic mechanisms of pulmonary fibrosis, few therapeutics have succeeded in the clinic, and they have failed to improve IPF patient survival. Areas covered: Based on a literature search and our own results, we discuss the key cellular and molecular responses that contribute to (myo)fibroblast actions and pulmonary fibrosis pathogenesis; this includes signaling pathways in various cells that aberrantly and persistently activate (myo)fibroblasts in fibrotic lesions and promote scar tissue formation in the lung. Expert opinion: Lessons learned from recent failures and successes with new therapeutics point toward approaches that can target multiple pro-fibrotic processes in IPF. Advances in preclinical modeling and single-cell genomics will also accelerate novel discoveries for effective treatment of IPF.