Abstract | BACKGROUND: OBJECTIVE: We sought to determine the in vivo effect of nasal exposure to SE on the development of AR using mouse model. METHODS: BALB/c mice were intranasally sensitized with Schistosoma mansoni egg antigen (SmEA) in the presence or absence of staphylococcal enterotoxin B (SEB). Control mice were intranasally sensitized with either SEB or SmEA alone. The production of antigen-specific antibodies including IgE, nasal eosinoplilia and cytokines by nasal mononuclear cells was compared among mice that had or had not received SEB treatment. RESULTS: Nasal exposure to SEB enhanced the development of AR in SmEA-sensitized mice, as manifested by SmEA-specific IgE production, nasal eosinophilia, and IL-4 and IL-5 production by nasal mononuclear cells after Ag challenge. This treatment also elicited IFN-gamma production by SmEA-primed cells. In addition, these mice produced SEB-specific IgE whereas mice treated with SEB without SmEA sensitization did not produce SEB-specific IgE or demonstrate nasal eosinophilia. CONCLUSION: These results suggest that the nasal exposure to SEB enhances susceptibility to AR although the exposure to SE solely does not induce AR.
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Authors | M Okano, H Hattori, T Yoshino, Y Sugata, M Yamamoto, T Fujiwara, A A Satoskar, A R Satoskar, K Nishizaki |
Journal | Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
(Clin Exp Allergy)
Vol. 35
Issue 4
Pg. 506-14
(Apr 2005)
ISSN: 0954-7894 [Print] England |
PMID | 15836761
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Allergens
- Enterotoxins
- Interleukin-5
- Interleukin-4
- Immunoglobulin E
- Interferon-gamma
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Topics |
- Allergens
(immunology)
- Animals
- Antibody Specificity
(immunology)
- Cells, Cultured
- Dose-Response Relationship, Immunologic
- Enterotoxins
(immunology)
- Eosinophilia
(immunology)
- Female
- Immunization
- Immunoglobulin E
(immunology)
- Interferon-gamma
(immunology)
- Interleukin-4
(immunology)
- Interleukin-5
(immunology)
- Mice
- Mice, Inbred BALB C
- Nose
- Respiratory Hypersensitivity
(immunology)
- Rhinitis
(immunology)
- Staphylococcus aureus
(immunology)
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