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Targeting neutrophil elastase in cystic fibrosis.

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Version 2 2021-12-17, 18:03
Version 1 2019-11-22, 16:35
journal contribution
posted on 2021-12-17, 18:03 authored by Emer Kelly, Catherine GreeneCatherine Greene, Noel G McElvaneyNoel G McElvaney

BACKGROUND: Cystic fibrosis (CF) is a lethal hereditary disease characterised by neutrophil-dominated lung inflammation. These abundant neutrophils produce neutrophil elastase (NE), a destructive serine protease that has direct actions on extracellular matrix proteins and has a role in the host response to inflammation and infection.

OBJECTIVE: This review examines the prospect of developing novel therapies for CF by targeting NE. The authors explore the functions of NE and of naturally-occurring and synthetic NE inhibitors.

METHODS: A literature search was conducted exploring the functions of NE and inhibitors of NE; naturally occurring and synthetic.

CONCLUSIONS: Targeting NE in CF offers therapeutic potential, but optimal inhibitors that can be delivered safely and effectively to the lung are still under development.

History

Comments

The Version of Scholarly Record of this Article is published Expert Opinion on Therapeutic Targets 2008, available online at: http://www.tandfonline.com/ DOI: 10.1517/14728222.12.2.145

Published Citation

Kelly E, Greene CM, McElvaney NG. Targeting neutrophil elastase in cystic fibrosis. Expert Opinion on Therapeutic Targets. 2008;12(2):145-57.

Publication Date

2008-02-01

PubMed ID

18208364

Department/Unit

  • Beaumont Hospital
  • Medicine

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