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Novel mechanisms and treatment of idiopathic pulmonary fibrosis

Research output: Contribution to journalArticlepeer-review

Abstract

Idiopathic pulmonary fibrosis (IPF) is a devastating progressive disease of unknown etiology that carries a grim prognosis. Over the last few decades there have been significant advances in our understanding of the mechanisms that drive the fibrotic process. In this review, we discuss the natural history of IPF, recent discoveries of the genetic factors and environmental and infectious exposures that influence the development and progression of the disease, and highlight some of the novel discoveries in our understanding of the mechanisms that govern lung fibrosis. Finally, we discuss the new and exciting therapies that are now available to manage this devastating illness.

Original languageEnglish (US)
Pages (from-to)145-153
Number of pages9
JournalDiscovery Medicine
Volume20
Issue number109
StatePublished - 2015

Bibliographical note

Publisher Copyright:
© Discovery Medicine.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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