Qu Yinfei, Yamada Takaya, Aoi Noriaki, Morikura Ichiro, Fuchiwaki Takafumi, Hotta Yukie, Prokopakis Emmanuel, Kawauchi Hideyuki
1 Department of Otolaryngology, Faculty of Medicine, Shimane University, Izumo city, Japan.
2 Department of Experimental Animals, Center for Integrated Research in Science, Shimane University, Izumo city, Japan.
Ann Otol Rhinol Laryngol. 2019 Jun;128(6_suppl):26S-35S. doi: 10.1177/0003489419835848.
Sublingual immunotherapy has been considered to be a painless and effective therapeutic treatment of patients with allergic rhinitis. Its mechanism of action has been elucidated, but there are still controversies among many reports between clinical efficacy and laboratory data. Therefore, its mechanism of action needs to be investigated further by using promising animal models such as rodents and monkeys.
Bearing this in mind, in our present study, we successfully constructed an effective murine model for sublingual immunotherapy (SLIT) in allergic rhinitis in which mice were sublingually administered ovalbumin (OVA), followed by intraperitoneal (ip) sensitization and intranasal (i.n.) challenge of OVA.
To summarize our experimental data, nasal symptoms such as sneezing and nasal rubbing of sublingually treated mice were significantly attenuated in accordance with lower specific IgE antibodies in sera. Histological analysis of eosinophil recruitment in nasal mucosae reveals less allergic inflammation in sublingually treated mice. Interleukin-10 (IL-10) production and IL-10-specific mRNA gene expression of cultured submandibular lymph node (SMLN) cells with OVA, obtained from sublingually treated mice, were significantly higher than those of mice without sublingual treatment.
These results demonstrate that sublingually introduced antigens can actually attenuate nasal symptoms in a murine allergic rhinitis model upon allergen exposures. Furthermore, our immunological data might indicate an important role of IL-10 producing T cells in SMLN to control nasal allergic reaction.
舌下免疫疗法被认为是治疗过敏性鼻炎患者的一种无痛且有效的治疗方法。其作用机制已得到阐明,但许多报告在临床疗效和实验室数据之间仍存在争议。因此,需要通过使用啮齿动物和猴子等有前景的动物模型进一步研究其作用机制。
考虑到这一点,在我们目前的研究中,我们成功构建了一种有效的过敏性鼻炎舌下免疫疗法(SLIT)小鼠模型,其中小鼠舌下给予卵清蛋白(OVA),随后腹腔内(ip)致敏和鼻内(i.n.)给予OVA激发。
总结我们的实验数据,舌下治疗小鼠的打喷嚏和鼻摩擦等鼻部症状随着血清中特异性IgE抗体降低而显著减轻。鼻黏膜中嗜酸性粒细胞募集的组织学分析显示,舌下治疗小鼠的过敏性炎症较少。从舌下治疗小鼠获得的用OVA培养的下颌下淋巴结(SMLN)细胞的白细胞介素-10(IL-10)产生和IL-10特异性mRNA基因表达显著高于未进行舌下治疗的小鼠。
这些结果表明,在过敏原暴露时,舌下引入的抗原实际上可以减轻小鼠过敏性鼻炎模型中的鼻部症状。此外,我们的免疫学数据可能表明SMLN中产生IL-10的T细胞在控制鼻过敏反应中起重要作用。