Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
J Korean Med Sci. 2021 Jan 18;36(3):e18. doi: 10.3346/jkms.2021.36.e18.
Generally, allergen immunotherapy must be administered for three to five years. Meanwhile, rush immunotherapy (RIT) shortens the required duration for the build-up phase, thereby improving the therapy's convenience compared with conventional immunotherapy (CIT). However, RIT is often performed with modified allergens. Therefore, this study aimed to investigate the safety and utility of RIT with aqueous allergens.
Medical records of 98 patients sensitized with at least one inhalant allergen who had received subcutaneous immunotherapy for allergic rhinitis with or without asthma were retrospectively reviewed. All patients were classified into three groups: depot-RIT (n = 25), receiving RIT with depot allergen; aqueous-RIT (n = 48), receiving RIT with aqueous allergen; and aqueous-CIT (n = 25), receiving CIT with aqueous allergen. Patients who had received immunotherapy targeting only house dust mites were excluded.
The proportions of patients presenting with a systemic reaction to depot-RIT, aqueous-RIT, or aqueous-CIT were 80.0%, 85.4%, and 48.0%, respectively ( = 0.002). The proportions of patients experiencing severe systemic reaction were 4.0%, 16.7%, and 8.0% in depot-RIT, aqueous-RIT and aqueous-CIT, respectively ( = 0.223). The proportions of depot-RIT and aqueous-RIT patients presenting with systemic reaction or severe systemic reaction did not differ significantly ( = 0.553 and = 0.118, respectively). Significantly fewer depot-RIT (1.0 ± 0.2) and aqueous-RIT patients (2.0 ± 1.3) required outpatient clinical visits during the build-up phase, compared to those administered aqueous-CIT (13.6 ± 1.9; < 0.001). Moreover, the build-up phase decreased to 17.4 ± 1.8 days in depot-RIT and 23.7 ± 10.9 days in aqueous-RIT, compared to 92.0 ± 12.5 days in aqueous-CIT ( < 0.001).
RIT with aqueous allergen reduced the build-up phase duration and frequency of hospital visits, with acceptable safety levels. RIT with aqueous allergen may, therefore, be suitable for broad application to patients with respiratory allergies.
通常情况下,变应原免疫治疗需要持续三到五年。同时,速发型免疫疗法(RIT)缩短了累积阶段所需的时间,与传统免疫疗法(CIT)相比,提高了治疗的便利性。然而,RIT 通常使用修饰变应原进行。因此,本研究旨在探讨用水溶液变应原进行 RIT 的安全性和实用性。
回顾性分析了 98 例至少对一种吸入性变应原过敏并接受皮下免疫治疗的变应性鼻炎合并或不合并哮喘患者的病历。所有患者分为三组:储库-RIT(n=25),接受储库变应原的 RIT;水溶液-RIT(n=48),接受水溶液变应原的 RIT;水溶液-CIT(n=25),接受水溶液变应原的 CIT。排除仅接受针对屋尘螨的免疫治疗的患者。
接受储库-RIT、水溶液-RIT 或水溶液-CIT 的患者中出现全身性反应的比例分别为 80.0%、85.4%和 48.0%(=0.002)。在储库-RIT、水溶液-RIT 和水溶液-CIT 中,出现严重全身性反应的患者比例分别为 4.0%、16.7%和 8.0%(=0.223)。储库-RIT 和水溶液-RIT 患者出现全身性反应或严重全身性反应的比例无显著差异(=0.553 和=0.118,分别)。在累积阶段,接受储库-RIT(1.0±0.2)和水溶液-RIT(2.0±1.3)的患者需要门诊临床就诊的次数明显少于接受水溶液-CIT(13.6±1.9;<0.001)。此外,储库-RIT 和水溶液-RIT 的累积阶段分别缩短至 17.4±1.8 天和 23.7±10.9 天,而水溶液-CIT 的累积阶段为 92.0±12.5 天(<0.001)。
用水溶液变应原进行 RIT 可减少累积阶段的持续时间和就诊次数,安全性水平可接受。因此,用水溶液变应原进行 RIT 可能适用于广泛的呼吸道过敏患者。