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Metalworking fluid with mycobacteria and endotoxin induces hypersensitivity pneumonitis in mice.

Authors: Thorne, PS  Adamcakova-Dodd, A  Kelly, KM  O'neill, ME  Duchaine, C 
Citation: Thorne PS, etal., Am J Respir Crit Care Med. 2006 Apr 1;173(7):759-68. Epub 2005 Dec 30.
Pubmed: (View Article at PubMed) PMID:16387809
DOI: Full-text: DOI:10.1164/rccm.200405-627OC

BACKGROUND: Human cases of hypersensitivity pneumonitis (HP) have been reported among machinists for over 10 yr. Although mycobacteria have been implicated as causal agents, this has not been established in experimental studies and the mechanisms remain unclear. Other constituents of in-use metalworking fluids (MWFs) may also contribute to the development of lung disease. We investigated the potential for Mycobacterium immunogenum (MI) in MWFs to induce HP. METHODS: Mice were exposed intranasally for 3 wk to MI (isolated from MWFs), Saccharopolyspora rectivirgula (positive control), saline, endotoxin, MWFs spiked with endotoxin and/or MI, used MWFs, and particulate-fortified used MWFs. Responses were assessed 96 h after the last exposure. RESULTS: Mice exposed to MI in MWFs developed lung pathology consistent with HP along with significantly more monocytes and neutrophils in lung lavage, increased CD4+/CD8+ T-lymphocyte ratio, and marked pulmonary lymphocytosis on histologic examination when compared with saline-treated control mice. Mice with Grade 2 or higher pathology (0-4 point scale) exhibited significantly elevated macrophage inflammatory protein-1alpha and IL-10 and a trend toward higher RANTES 96 h after the final dose. Endotoxin coexposure augmented lung pathology. CONCLUSION: MWFs containing mycobacteria induced granulomatous lung lesions, peribronchiolar lymphocytosis, increased cell concentrations in lavage, and up-regulation of several cytokines. These findings are consistent with HP.


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CRRD Object Information
CRRD ID: 4891434
Created: 2011-01-13
Species: All species
Last Modified: 2011-01-13
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.