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Dose-Dependent Immunological Responses after a 6-Month Course of Sublingual House Dust Mite Immunotherapy in Patients with Allergic Rhinitis

机译:变应性鼻炎患者舌下房尘螨免疫治疗6个月疗程后的剂量依赖性免疫反应

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Background: House dust mite (HDM) immunotherapy has proven efficacy in treating allergic rhinitis (AR) symptoms. This trial evaluated the dose-response relationship of SLITone(ULTRA (R)) HDM mix based on immunological parameters and safety in subjects with moderate-to-severe HDM AR not controlled by symptomatic medication. Materials and Methods: A randomized, parallel-group, open-label, clinical trial compared 50/150/300 standard reactivity unit (SRU) doses of SLITone(ULTRA (R)) HDM mix for 6 months. Subjects had moderate-to-severe HDM AR, positive skin prick and IgE against Dermatophagoides pteronyssinus/Dermatophagoides farinae (DP/DF). The primary end point was change from baseline in the IgE-blocking factor against DP after 6 months. Secondary end points measured changes in the IgE-blocking factor for DP at 3 months and for DF at 3 and 6 months, and in IgG(4) and specific IgE to DP/DF after 3 and 6 months. Tolerability was assessed through the evaluation of all adverse events (AEs). Results: A total of 219 subjects were randomized and 196 completed the trial. Dose effect was significant on DP IgE-BF after 6 months (p = 0.018). The change in the DP IgE-blocking factor at a 300-SRU dose was higher than at other doses after 3 (p = 0.008) and 6 (p = 0005) months of treatment. Similar changes were observed for IgG(4) and allergen-specific IgE. The number of AEs increased with the dose and were mild-to-moderate, with no severe treatment-related AEs reported. The most frequent AEs were oral/tongue pruritus, mouth oedema and abdominal upper pain. Conclusions: Data showed a dose-response for immunological markers and safety with a better immunological response for 300 SRU. The highest dose (300 SRU daily) was considered as the optimal maintenance dose. (C) 2016 The Author(s) Published by S. Karger AG, Basel
机译:背景:屋尘螨(HDM)免疫疗法已被证明可治疗过敏性鼻炎(AR)症状。该试验基于免疫学参数和安全性,对中度至重度HDM AR不受对症药物控制的受试者,评估了SLITone(ULTRA)HDM混合物的剂量反应关系。材料和方法:一项随机,平行分组,开放标签的临床试验比较了SLITone(ULTRA)HDM混合物的50/150/300标准反应单位(SRU)剂量6个月。受试者患有中度至重度的HDM AR,阳性皮肤点刺和抗粉虱Dermatophagossinus / Dermatophagoides farinae(DP / DF)的IgE。主要终点是6个月后针对DP的IgE阻断因子相对于基线的变化。次要终点测量了3个月时DP的IgE阻断因子的变化以及3个月和6个月DF的IgE阻断因子的变化,以及3个月和6个月后IgG(4)和DP / DF的特异性IgE的变化。通过评估所有不良事件(AE)评估耐受性。结果:总共219名受试者被随机分组​​,其中196名完成了试验。 6个月后,剂量对DP IgE-BF显着(p = 0.018)。在治疗3个月(p = 0.008)和6个月(p = 0005)后,在300-SRU剂量下DP IgE阻断因子的变化高于其他剂量。 IgG(4)和过敏原特异性IgE观察到相似的变化。不良事件的数量随剂量增加而增加,为轻度至中度,没有严重的治疗相关不良事件的报道。最常见的不良事件是口腔/舌部瘙痒,口腔水肿和腹部上痛。结论:数据显示免疫标记物的剂量反应和安全性,对300 SRU的免疫反应更好。最高剂量(每天300 SRU)被认为是最佳维持剂量。 (C)2016作者由巴塞尔S. Karger AG发布

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