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Cross sectional study on cytokine production (TNF- , IL-8) in German coalminers with progressive massive fibrosis and in control miners using a rapid wholeblood assay

Whole-blood release of tumour necrosis factor (TNF- ) and interleukin 8 (IL-8) was studied in 26 German ex-coalminers with progressive massive fibrosis (≥A, ILO 1980; cases) and 26 ex-miners free of pneumoconiosis (≤ 0/1; controls) using a simple wholeblood assay. Cases and controls were matched ind...

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Bibliographic Details
Published in:Biomarkers 2001, Vol.6 (6), p.428-439
Main Author: Morfeld, P. J. A. Borm, R. P. F. Schins, H. Lenaerts, B. Witte, R. Derwall, C. Piekarski, P.
Format: Article
Language:English
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Summary:Whole-blood release of tumour necrosis factor (TNF- ) and interleukin 8 (IL-8) was studied in 26 German ex-coalminers with progressive massive fibrosis (≥A, ILO 1980; cases) and 26 ex-miners free of pneumoconiosis (≤ 0/1; controls) using a simple wholeblood assay. Cases and controls were matched individually by age and duration of coalmine dust exposure (5-year window). Whole-blood cytokine release was determined (blinded to case control status) in incubations without additions (spontaneous) and with endotoxin (LPS, 3 ng ml-1) or with coalmine dust (CMD; 5 mg ml-1). CMD-stimulated TNF- release was significantly increased and LPS-induced IL-8 release was significantly decreased in cases (matched t-tests: p < 0.01). No effect of duration of exposure was detectable in an unmatched analysis. No clear relationship with lung function parameters independent from case/control-status was observed, although a possible positive association with central airway resistance was indicated by multiple regression for both CMD stimulated TNF- and LPS-stimulated IL-8. This study on individually matched coalminers validates previous findings on monocyte TNF release as a marker for pneumoconiosis using a method (whole-blood assay) that is more feasible for epidemiological studies. The different response of TNF- and IL-8 may be useful in studying the occurrence of different endpoints like pneumoconiosis and lung function decrease.
ISSN:1354-750X
1366-5804
DOI:10.1080/13547500110066623