RESUMO
BACKGROUND: We reported that level of lipopolysaccharide (LPS) exposure determined the type of airway inflammation in a murine model of asthma. OBJECTIVE: The purpose of this study is to evaluated the role of IL-13 in low dose LPS induced murine model of asthma using IL-13 and signal transducer and activator of transcription 6 (STAT6) deficient mice. METHODS: Mice were sensitized with an intranasal application of LPS-depleted ovalbumin (OA) and different doses of LPS (0.1 and 10 µg), and then challenged intranasally with OA alone. The phenotype changes between wild type (WT) and IL-13(-/-) mice and between WT and STAT6(-/-) mice were evaluated. RESULTS: We confirmed again that low and high dose LPS resulted in different phenotypes of murine asthma. In the present study, we observed that phenotypes of murine asthma induced by low dose LPS were abolished in the homozygous null mutation of the IL-13 and STAT6 gene. However, those changes were not shown in mice sensitized OA plus high dose LPS. CONCLUSION: IL-13 plays an important role in low dose LPS induced murine model of asthma. Our results provided a new insight in understanding of the potential role of IL-13 in innate immunity in human allergic asthma.
RESUMO
The two-spotted mite (TSM) is commonly found on fruit trees, herbaceous plants, and greenhouse flowers. However, a recent investigation indicated that the sensitization rate to TSM was as high as that of house-dust mites (HDMs) in nonfarmers as well as in farmers working in orchards in this country. The aim of this study was to identify immunoglobulin E (IgE)-binding components within TSM and to evaluate the allergenic relationship with the citrus red mite (CRM) and HDM. Sera were collected from eight patients who were not farmers and who had asthma with high serum-specific IgE to the TSM and from unexposed controls showing negative responses to the TSM on skin-prick test. Twelve percent sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblot analysis were applied. To evaluate allergenic relationships with HDMs and CRMs, two kinds of sera pools were used: one (A) showing positive responses to both TSMs and HDMs and the other (B) showing an isolated positive response to TSMs. ELISA inhibition tests using A and B pooled sera were conducted. The TSM-ELISA inhibition test using sera A showed significant inhibition with addition of TSMs and CRMs, partial inhibition with HDMs, and minimal inhibition with other inhalant allergens. The ELISA inhibition test using sera B showed significant inhibition with TSMs and CRMs and minimal inhibition was noted with HDMs as well as other inhalant allergens. Immunoblot analysis using individual sera showed seven IgE-binding components (75, 56, 47, 41, 37, 28, and 14 kDa) and two (75 and 14 kDa) of them were bound to IgE in > 50% of the sera tested. Seven IgE-binding components were identified within the TSM extract and two (75 and 14 kDa) could be considered major allergens. It is suggested that the TSM contains species-specific allergen in addition to shared allergens with CRMs and HDMs.
