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扁桃体内免疫疗法:变应性鼻炎皮下免疫疗法的一种便捷有效替代方法

Intratonsillar Immunotherapy: A Convenient and Effective Alternative to Subcutaneous Immunotherapy for Allergic Rhinitis.

作者信息

Gu Tian, Zhang Wei, Tan Lu, Xiang Rong, Liu Peiqiang, Huang Jingyu, Deng Qin, Deng Yuqin, Tao Zezhang, Chen Shiming, Xu Yu

机构信息

Department of Rhinology and Allergy, Otolaryngology-Head and Neck Surgery Center, Renmin Hospital of Wuhan University, Wuhan 430060, China.

Research Institute of Otolaryngology-Head and Neck Surgery, Renmin Hospital of Wuhan University, Wuhan, China.

出版信息

Research (Wash D C). 2025 Jan 16;8:0573. doi: 10.34133/research.0573. eCollection 2025.

DOI:10.34133/research.0573
PMID:39822282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11735709/
Abstract

Allergen-specific immunotherapy (AIT) is the only treatment that addresses the root cause of immunoglobulin E (IgE)-mediated allergies, but conventional methods face challenges with treatment duration, patient compliance, and adverse effects. In this study, we propose intratonsillar immunotherapy (ITIT) as a new effective and safer route for AIT. Prior to clinical trials, we analyzed tonsil samples from human subjects to assess immune responses, measuring interleukin-4 (IL-4), IL-21, total IgE (tIgE), and allergen-specific IgE concentrations using ELISA and BioIC. Our results indicated that tonsils contained higher levels of allergen-specific IgE compared to peripheral blood. In the clinical phase, 120 allergic rhinitis (AR) patients were treated with either 3 intratonsillar allergen injections over 2 months or conventional subcutaneous immunotherapy (SCIT) over 1 year. ITIT demonstrated superior and faster symptom relief, especially in younger patients, while requiring markedly fewer doses and injections than SCIT. Immunological analysis revealed reduced eosinophil counts, increased regulatory T (T) and follicular regulatory T (T) cell levels, and a favorable shift in cytokine profiles. Adverse events were minimal, and the treatment showed high patient compliance. These findings suggest that ITIT could provide an effective, safer, and more convenient alternative to AIT.

摘要

变应原特异性免疫疗法(AIT)是唯一能解决免疫球蛋白E(IgE)介导的过敏症根本原因的治疗方法,但传统方法在治疗持续时间、患者依从性和不良反应方面面临挑战。在本研究中,我们提出扁桃体内免疫疗法(ITIT)作为AIT一种新的有效且更安全的途径。在进行临床试验之前,我们分析了人类受试者的扁桃体样本以评估免疫反应,使用酶联免疫吸附测定(ELISA)和生物免疫芯片(BioIC)测量白细胞介素-4(IL-4)、IL-21、总IgE(tIgE)和变应原特异性IgE浓度。我们的结果表明,与外周血相比,扁桃体中变应原特异性IgE水平更高。在临床阶段,120名变应性鼻炎(AR)患者接受了为期2个月的3次扁桃体内变应原注射治疗或为期1年的传统皮下免疫疗法(SCIT)。ITIT显示出更优且更快的症状缓解效果,尤其是在年轻患者中,同时所需的剂量和注射次数明显少于SCIT。免疫学分析显示嗜酸性粒细胞计数减少、调节性T(T)细胞和滤泡调节性T(T)细胞水平增加,并且细胞因子谱发生有利变化。不良事件极少,且该治疗显示出较高的患者依从性。这些发现表明,ITIT可为AIT提供一种有效、更安全且更便捷的替代方法。

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