Okano M, Hattori H, Yoshino T, Sugata Y, Yamamoto M, Fujiwara T, Satoskar A A, Satoskar A R, Nishizaki K
Otolaryngology-Head & Neck Surgery, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan.
Clin Exp Allergy. 2005 Apr;35(4):506-14. doi: 10.1111/j.1365-2222.2005.02195.x.
Staphylococcal enterotoxins (SEs) appear to play a role in the pathogenesis of allergic disease. However, little is known whether the nasal exposure to SE affects the development of allergic rhinitis (AR).
We sought to determine the in vivo effect of nasal exposure to SE on the development of AR using mouse model.
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.
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.
These results suggest that the nasal exposure to SEB enhances susceptibility to AR although the exposure to SE solely does not induce AR.
葡萄球菌肠毒素(SEs)似乎在变应性疾病的发病机制中起作用。然而,关于经鼻暴露于SEs是否会影响变应性鼻炎(AR)的发生发展,人们了解甚少。
我们试图使用小鼠模型确定经鼻暴露于SEs对AR发生发展的体内影响。
在存在或不存在葡萄球菌肠毒素B(SEB)的情况下,用曼氏血吸虫卵抗原(SmEA)对BALB/c小鼠进行鼻内致敏。对照小鼠分别单独用SEB或SmEA进行鼻内致敏。比较接受或未接受SEB治疗的小鼠中抗原特异性抗体(包括IgE)的产生、鼻内嗜酸性粒细胞增多以及鼻单核细胞产生的细胞因子。
经鼻暴露于SEB可增强SmEA致敏小鼠中AR的发生发展,表现为在抗原激发后SmEA特异性IgE的产生、鼻内嗜酸性粒细胞增多以及鼻单核细胞产生IL-4和IL-5。这种治疗还引发了SmEA致敏细胞产生IFN-γ。此外,这些小鼠产生了SEB特异性IgE,而未用SmEA致敏仅用SEB治疗的小鼠未产生SEB特异性IgE,也未出现鼻内嗜酸性粒细胞增多。
这些结果表明,经鼻暴露于SEB会增加对AR的易感性,尽管单独暴露于SEs不会诱发AR。