Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comment
. 2008 Apr 29;5(4):e98.
doi: 10.1371/journal.pmed.0050098.

A blood test for lung fibrosis

Affiliations
Comment

A blood test for lung fibrosis

Peter J Barnes. PLoS Med. .

Abstract

Peter Barnes discusses a new study on the role of two matrix metalloproteinases, MMP1 (collagenase) and MMP7 (matrilysin), as possible biomarkers of idiopathic pulmonary fibrosis.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: The author has declared that no competing interests exist.

Figures

Figure 1
Figure 1. Mechanisms of IPF
Injury of alveolar epithelial cells releases fibrogenic mediators, such as TGF-β, which stimulate myofibroblasts to produce extracellular matrix proteins. Matrix metalloproteinases MMP1 and MMP7 are also produced and may reflect tissue remodelling or contribute to fibrosis through recruitment of neutrophils, which release reactive oxygen species and TGF-β. Increased plasma concentrations of MMPs may therefore reflect increased extracellular matrix turnover and disease activity.

Comment on

References

    1. Strieter RM. Pathogenesis and natural history of usual interstitial pneumonia: The whole story or the last chapter of a long novel. Chest. 2005;128:526S–532S. - PubMed
    1. Selman M, King TE, Pardo A. Idiopathic pulmonary fibrosis: Prevailing and evolving hypotheses about its pathogenesis and implications for therapy. Ann Intern Med. 2001;134:136–151. - PubMed
    1. Maher TM, Wells AU, Laurent GJ. Idiopathic pulmonary fibrosis: Multiple causes and multiple mechanisms. Eur Respir J. 2007;30:835–839. - PubMed
    1. Lawson WE, Loyd JE. The genetic approach in pulmonary fibrosis: Can it provide clues to this complex disease. Proc Am Thorac Soc. 2006;3:345–349. - PMC - PubMed
    1. Selman M, Pardo A, Barrera L, Estrada A, Watson SR, et al. Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis. Am J Respir Crit Care Med. 2006;173:188–198. - PMC - PubMed

MeSH terms