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Mouse strain differences in eosinophilic airway inflammation caused by intratracheal instillation of mite allergen and diesel exhaust particles.
- Source :
-
Journal of applied toxicology : JAT [J Appl Toxicol] 2004 Jan-Feb; Vol. 24 (1), pp. 69-76. - Publication Year :
- 2004
-
Abstract
- Response differences by different strains of mice towards house dust mites (Dermatophagoides farinae) or diesel exhaust particles (DEP) were investigated. Mouse strains BALB/c, ICR and C3H/He received 1 micro g of D. farinae or 1 microg of D. farinae + 50 microg of DEP intratracheally four times at 2-week intervals. Dermatophagoides farinae treatment caused the recruitment of eosinophils and lymphocytes. The order of magnitude of the eosinophilic airway inflammation was BALB/c < ICR < C3H/He mice. The protein levels of eotaxin and IL-5 in lung tissues correlated with the manifestations of eosinophilic airway inflammation by D. farinae administration. Diesel exhaust particles aggravated the manifestation of the eosinophilic inflammation through goblet cell proliferation in the airway and enhanced the local expression of eotaxin and IL-5 in all three strains of mice. The levels of eotaxin and IL-5 in lung tissues corresponded to the pathological changes caused by D. farinae + DEP. The increasing order of production levels of antigen-specific IgG1 by D. farinae or D. farinae + DEP was BALB/c < ICR < C3H/He mice. The significant adjuvant effect of DEP on IgG1 production was observed in the C3H/He mice (P < 0.05). These results suggest that the murine strain differences in the production of eosinophilic airway inflammation by D. farinae + DEP are related to differences in local expression of IL-5 and eotaxin. The enhancing effects of DEP may be mediated by a cytokine increase in the local expression. Antigen-specific IgG1 may be an important immunoglobulin in the pathogenesis of allergic asthma enhanced by DEP.<br /> (Copyright 2004 John Wiley & Sons, Ltd.)
- Subjects :
- Animals
Antigens, Dermatophagoides administration & dosage
Asthma metabolism
Asthma pathology
Chemokine CCL11
Chemokines, CC metabolism
Chemotactic Factors, Eosinophil metabolism
Disease Models, Animal
Dose-Response Relationship, Immunologic
Drug Therapy, Combination
Dust
Immunoenzyme Techniques
Interleukin-5 metabolism
Intubation, Intratracheal
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Mice, Inbred ICR
Pulmonary Eosinophilia metabolism
Pulmonary Eosinophilia pathology
Species Specificity
Allergens adverse effects
Antigens, Dermatophagoides adverse effects
Asthma chemically induced
Pulmonary Eosinophilia chemically induced
Pyroglyphidae immunology
Vehicle Emissions adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 0260-437X
- Volume :
- 24
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of applied toxicology : JAT
- Publication Type :
- Academic Journal
- Accession number :
- 14745849
- Full Text :
- https://doi.org/10.1002/jat.949