致编辑的信关于“舌下免疫疗法通过诱导下颌下淋巴结产生IL-10的T细胞减轻小鼠变应性鼻炎模型中过敏原暴露后的鼻症状”

Guanyang Kang
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引用次数: 0

摘要

尊敬的编辑,我立即非常关注和感兴趣地阅读了最近在该杂志上发表的Qu及其同事的一篇重要而美观的文章,题为“通过诱导下颌淋巴结产生IL-10的T细胞,舌下免疫治疗减轻小鼠变应性鼻炎模型中过敏原暴露后的鼻症状”。证明舌下引入的抗原实际上可以减轻小鼠变应性鼻炎模型在过敏原暴露后的鼻症状。此外,他们的免疫学数据可能表明下颌下淋巴结中产生白细胞介素-10的T细胞在控制鼻过敏反应中起重要作用。我们完全同意他们具有里程碑意义的结论。其研究可为鼻炎的治疗提供宝贵的经验。有令人信服的证据表明鼻炎和哮喘之间有密切的关系。流行病学研究表明,大多数哮喘患者伴有鼻炎,鼻炎的存在是哮喘发展的一个增加的危险因素。哮喘和鼻炎患者具有共同的生理病理机制,包括气道高反应性增强和对大量刺激的反应性增强。治疗研究表明,治疗鼻炎可以改善哮喘,反之亦然。最近,在Boonpiyathad的研究中,高海拔哮喘治疗同时改善了哮喘控制,1秒用力呼气量(FEV1)和呼出一氧化氮(FeNO),同时改变了已知有助于嗜酸性粒细胞和过敏性炎症的效应细胞的免疫学特性。因此,我们假设高原治疗是治疗鼻炎的有效方法。高原治疗是一种公认的治疗选择,可改善哮喘患者的临床症状。研究表明,高原治疗可以减少哮喘患者气道局部炎症和T细胞和单核细胞的全身活化。此外,研究表明,避免过敏原并不是高原治疗的唯一因素,似乎除过敏原特异性T细胞外的其他细胞也有助于有益的治疗效果。高海拔治疗哮喘患者的疗效可以用以下几种机制来解释:室内尘螨过敏原水平随着海拔的升高而降低(避免过敏原),远离压力和工作或家庭相关冲突(减少精神压力),颗粒暴露较少,皮质醇和儿茶酚胺水平升高,干燥的空气和高紫外线照射。所有这些机制都被认为对鼻炎的治疗有益。高原治疗鼻炎的安全性和有效性还需要进一步的研究。这些知识不仅可以加强高海拔对鼻炎的临床相关性,还可以提供治疗建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Letter to the Editor Regarding “Sublingual Immunotherapy Attenuates Nasal Symptoms upon Allergen Exposure in Murine Allergic Rhinitis Model via an Induction of IL-10 producing T cells in Submandibular Lymph Node”
Dear Editor, I immediately read with great attention and interest the significant and well-presented article recently published in an issue of this journal by Qu and colleagues entitled “Sublingual Immunotherapy Attenuates Nasal Symptoms upon Allergen Exposure in Murine Allergic Rhinitis Model via an Induction of IL-10 producing T cells in Submandibular Lymph Node”, demonstrating that sublingually introduced antigens can actually attenuate nasal symptoms in a murine allergic rhinitis model upon allergen exposures. Furthermore, their immunological data might indicate an important role of Interleukin-10 producing T cells in submandibular lymph node to control nasal allergic reaction. We completely agree with their landmark conclusions. Their study can provide valuable lessons for the therapy of rhinitis. There is compelling evidence of a close relationship between rhinitis and asthma. Epidemiological studies have shown that most of patients with asthma have concomitant rhinitis and the presence of rhinitis is an increased risk factor for development of asthma. Patients with asthma and rhinitis share common physiopathologic mechanism including heightened airway hyperresponsiveness and heightened reactivity to lots of stimuli. Therapeutic studies have demonstrated that the treatment of rhinitis can improve asthma and vice versa. Recently, in Boonpiyathad’s study, asthma treatment in high altitude simultaneously improved asthma control, forced expiratory volume in 1 second (FEV1) and exhaled nitric oxide (FeNO), while modifying the immunological characteristics of effector cells known to contribute to eosinophilic and allergic inflammation. Accordingly, we hypothesize that high altitude therapy is an effective treatment for rhinitis. High altitude therapy is a well-established therapeutic option, which improves clinical symptoms in the patients with asthma. Research studies have indicated that high altitude therapy can reduce the local airway inflammation and systemic activation of T cells and monocytes in asthma patients. Furthermore, it is shown that allergen avoidance is not the only factor in high altitude therapy, it appears possible that cells other than allergen-specific T cells also contribute to the beneficial treatment effect. The efficacy of high altitude therapy in treating asthma patients can be explained by several mechanisms: house dust mites allergen level decreases as altitude increases (allergen avoidance), moving away from stress and work or family-related conflicts (less mental stress), less particle exposure, increased cortisol and catecholamine level, the dry air and high ultraviolet light exposure. All these mechanisms are thought to be beneficial to the therapy of rhinitis. Additional studies are indeed needed to investigate the safety and effectiveness of high altitude therapy for rhinitis. Such knowledge would not only reinforce the clinical relevance of high altitude effects on rhinitis but also enable therapeutic recommendations.
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