Abstract
Idiopathic pulmonary fibrosis (IPF) is a persistent and an aggravating interstitial alveolar disease, marked by thickening and scarring of the lung parenchyma with unknown etiology leading to early death among the elderly population worldwide. The vast knowledge on the understanding of the pathogenesis, diagnosis, and therapeutic management has been raised significantly in recent years to delay the progression of IPF. Currently, nintedanib and pirfenidone are two medications used to treat IPF which significantly restores the alveolar epithelial functions; however, it is associated with a few demerits. Thus, new approaches are needed to overcome hurdles raised from IPF pathogenesis. Up-to-date approaches in pulmonary rehabilitation, non-pharmacological strategies, lung transplantation, and comorbidity management are mainly involved in subsiding the symptoms and thereby attempt to improve patient’s health outcomes. Hence clinical trial studies are in search of novel molecular and cellular targets to overcome IPF. This chapter highlights the understanding of up-to-date molecular and cellular targets and potential approaches which will create an avenue to design and develop novel therapeutics to defend against this complex and injurious disease.
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The work was supported in part by TRR fund, SASTRA Deemed-to-be University, Thanjavur, Tamilnadu, India.
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Sivanantham, B., Bose, V. (2021). Targeting Molecular and Cellular Mechanisms in Idiopathic Pulmonary Fibrosis. In: Dua, K., Löbenberg, R., Malheiros Luzo, Â.C., Shukla, S., Satija, S. (eds) Targeting Cellular Signalling Pathways in Lung Diseases. Springer, Singapore. https://doi.org/10.1007/978-981-33-6827-9_12
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