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Exposure and immunological determinants in a murine model for toluene diisocyanate (TDI) asthma.

Authors
Matheson-JM; Johnson-VJ; Vallyathan-V; Luster-MI
Source
Toxicol Sci 2005 Mar; 84(1):88-98
NIOSHTIC No.
20026187
Abstract
Isocyanate-induced asthma, the most commonly reported cause of occupational asthma, has been difficult to diagnose and control, in part, because the biological mechanisms responsible for the disease and the determinants of exposure have been difficult to define. Appropriate animals models of isocyanate asthma will be instrumental to further our understanding of this disease. Previous studies have demonstrated that dermal exposure to isocyanates in mice results in systemic sensitization that leads to eosinophilic airways inflammation upon subsequent airway challenge. We hypothesized that inhalation of vapor phase toluene diisocyante (TDI) will lead to immunologic sensitization in mice and that subsequent challenge will induce pathology and immune system alterations indicative of asthma found in humans. To determine the impact of exposure dose as well as the involvement of immune (allergic) or nonimmune mechanisms, a murine model of TDI asthma was established and characterized following either low-level subchronic or high-dose acute inhalation TDI exposure. C57BL/6 J mice were exposed to TDI by inhalation either subchronically for 6 weeks (20 ppb, 4 h/day, 5 days/week) or by a 2-h acute exposure at 500 ppb. Both groups were challenged 14 days later via inhalation with 20 ppb TDI for 1 h. Mice that underwent the subchronic exposure regimen demonstrated a marked allergic response evidenced by increases in airway inflammation, eosinophilia, goblet cell metaplasia, epithelial cell alterations, airway hyperreponsiveness (AHR), T(H)1/T(H)2 cytokine expression in the lung, elevated levels of serum IgE, and TDI-specific IgG antibodies, as well as the ability to transfer these pathologies to naive mice with lymphocytes or sera from TDI exposed mice. In contrast, mice that received acute TDI exposure demonstrated increased AHR, specific IgG antibodies, and pathology in the lung consistent with asthma, but without the presence of elevated serum IgE, lung eosionophilia, or increased expression of T(H) cytokines. These results describe mouse models for TDI asthma consistent with that found in workers with occupational asthma and indicate that the pulmonary pathology associated with TDI can vary depending upon the exposure paradigm.
Keywords
Models; Bronchial-asthma; Isocyanates; Occupational-diseases; Laboratory-animals; Animals; Animal-studies; Exposure-levels; Exposure-assessment; Sensitization; Airway-obstruction; Airway-resistance; Inhalation-studies; Immunologic-disorders; Immune-system-disorders; Immunology; Respiratory-system-disorders; Pulmonary-system-disorders
Contact
Toxicology and Molecular Biology Branch and Pathology and Physiology Research Branch, 1095 Willowdale Road, Morgantown, WV 26505
CODEN
TOSCF2
CAS No.
108-88-3
Publication Date
20050301
Document Type
Journal Article
Email Address
mluster@cdc.gov
Fiscal Year
2005
NTIS Accession No.
NTIS Price
Issue of Publication
1
ISSN
1096-6080
NIOSH Division
HELD
Priority Area
Disease and Injury: Asthma and Chronic Obstructive Pulmonary Disease
Source Name
Toxicological Sciences
State
WV
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