Aurélie Nihoul

Catholic University of Louvain, Walloon Region, Belgium

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Publications (1)3.09 Total impact

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    ABSTRACT: It has been generally well accepted that chronic inflammation is a necessary component of lung fibrosis but this concept has recently been challenged. Using biochemical, histological, immunohistochemistry, and cellular analyses, we compared the lung responses (inflammation and fibrosis) to fibrogenic silica particles (2.5 and 25 mg/g lung) in Sprague-Dawley rats and NMRI mice. Rats treated with silica particles developed chronic and progressive inflammation accompanied by an overproduction of TNF-alpha as well as an intense lung fibrosis. Dexamethasone or pioglitazone limited the amplitude of the lung fibrotic reaction to silica in rats, supporting the paradigm that inflammation drives lung fibrosis. In striking contrast, in mice, silica induced only a limited and transient inflammation without TNF-alpha overproduction. However, mice developed lung fibrosis of a similar intensity than rats. The fibrotic response in mice was accompanied by a high expression of the anti-inflammatory and fibrotic cytokine IL-10 by silica-activated lung macrophages. In mice, IL-10 was induced only by fibrotic particles and significantly expressed in the lung of silica-sensitive but not silica-resistant strains of mice. Anti-inflammatory treatments did not control lung fibrosis in mice. These results indicate that, beside chronic lung inflammation, a pronounced anti-inflammatory reaction may also contribute to the extension of silica-induced lung fibrosis and represents an alternative pathway leading to lung fibrosis.
    Full-text · Article · Feb 2005 · Respiratory research

Publication Stats

42 Citations
3.09 Total Impact Points

Top Journals


  • 2005
    • Catholic University of Louvain
      • Department of Industrial Toxicology and Occupational Medecine
      Walloon Region, Belgium