Levels of cathepsins S and H in pleural fluids of inflammatory and neoplastic origin
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Biomarkers blood metabolism MeSH
- Cysteine Endopeptidases blood metabolism MeSH
- Cathepsin H MeSH
- Cathepsins blood metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- Pleural Effusion, Malignant enzymology MeSH
- Biomarkers, Tumor blood metabolism MeSH
- Lung Neoplasms enzymology MeSH
- Paraneoplastic Syndromes enzymology MeSH
- Pleural Effusion enzymology MeSH
- Pleurisy enzymology MeSH
- Aged MeSH
- Inflammation enzymology MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- cathepsin S MeSH Browser
- CTSH protein, human MeSH Browser
- Cysteine Endopeptidases MeSH
- Cathepsin H MeSH
- Cathepsins MeSH
- Biomarkers, Tumor MeSH
Cathepsins S and H are present in immune cells and tissues and may play a role in the activation of an adoptive immune response. Our goal was to assess their protein levels in pleural fluids from 82 patients who underwent thoracentesis or thoracoscopy for therapeutic or diagnostic reasons and to relate them to an inflammatory, neoplastic or hemodynamic origin. Pleural effusions were also analyzed for a panel of 13 inflammatory or proliferative markers to test possible links to a nonspecific host reaction. Increased levels of cathepsin S were found in parainflammatory and cancer-related effusions compared to transudates. Cathepsin H levels were elevated only in parainflammatory effusions, whereas the levels in cancer-related effusions were comparable to transudates. Cathepsin S values significantly correlated with LDH, alpha-1-AT, VEGF, sICAM, sVCAM, MPO, uPA, MMP-9/TIMP-1, IL-8 and MCP-1, but not with CRP, IL-10 or cathepsin H. In contrast to cathepsin S, cathepsin H values did not correlate with markers of inflammation, indicating a specific role for cathepsin H in the pleural host response. In conclusion, the estimation of cathepsin S and cathepsin H may help to distinguish between effusions of different etiology.
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