首页> 外文期刊>The Journal of Allergy and Clinical Immunology >High-dose sublingual immunotherapy with single-dose aqueous grass pollen extract in children is effective and safe: A double-blind, placebo-controlled study
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High-dose sublingual immunotherapy with single-dose aqueous grass pollen extract in children is effective and safe: A double-blind, placebo-controlled study

机译:单剂量水草花粉提取物对儿童的大剂量舌下免疫疗法是安全有效的:一项双盲,安慰剂对照研究

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Background: Sublingual allergen-specific immunotherapy is a viable alternative to subcutaneous immunotherapy particularly attractive for use in children. Objective: This study investigated efficacy and safety of high-dose sublingual immunotherapy (SLIT) in children allergic to grass pollen in a randomized, double-blind, placebo-controlled trial. Methods: After a baseline seasonal observation, 207 children aged 4 to 12 years with grass pollen-allergic rhinitis/ rhinoconjunctivitis with/without bronchial asthma (Global Initiative for Asthma I/II) received either high-dose grass pollen SLIT or placebo daily for 1 pre-/co-seasonal period. The primary end point was the change of the area under the curve of the symptom-medication score (SMS) from the baseline season to the first season after start of treatment. Secondary outcomes were well days, responders, immunologic changes, and safety. Results: Mean changes in the area under the curve of the SMS from the baseline to the first grass pollen season after the start of treatment were -212.5 for the active group and -97.8 for the placebo group (P =.0040). Rhinoconjunctivitis SMS (P =.0020) and separated symptom and medication scores were also statistically different between the 2 groups (P = .0121 and P = .0226, respectively). The number of well days and the percentage of responders were greater in the active group. Changes in allergen-specific IgE and IgG levels indicated a significant immunologic effect. The treatment was well tolerated, and no serious treatment-related events were reported. Conclusions: This study confirmed that this SLIT preparation significantly reduced symptoms and medication use in children with grass pollen-allergic rhinoconjunctivitis. The preparation showed significant effects on allergen-specific antibodies, was well tolerated, and appeared to be a valid therapeutic option in children allergic to grass pollen. This trial was registered at www.clinicaltrials.gov as NCT00841256. (J Allergy Clin Immunol 2012;130:886-93.)
机译:背景:舌下变应原特异性免疫疗法是皮下免疫疗法的可行替代方案,特别适合儿童使用。目的:本研究在一项随机,双盲,安慰剂对照试验中研究了大剂量舌下免疫疗法(SLIT)对草花粉过敏儿童的疗效和安全性。方法:在基线季节观察之后,207名4到12岁的患有花粉过敏性鼻炎/鼻结膜炎伴/不伴支气管哮喘的儿童(哮喘I / II全球倡议)每天接受大剂量草粉SLIT或安慰剂治疗1季前/季前。主要终点是治疗开始后从基线季节到第一个季节的症状药物评分(SMS)曲线下面积的变化。次要结果是好日子,反应者,免疫学改变和安全性。结果:治疗开始后,从基线到第一个草花粉季节,SMS曲线下面积的平均变化为活动组为-212.5,安慰剂组为-97.8(P = .0040)。两组之间的鼻结膜炎SMS(P = .0020)和单独的症状和用药得分也有统计学差异(分别为P = .0121和P = .0226)。在活动组中,天数和响应者的百分比更高。变应原特异性IgE和IgG水平的变化表明具有明显的免疫学作用。该治疗耐受性良好,没有报道严重的治疗相关事件。结论:这项研究证实,这种SLIT制剂可显着减少草花粉过敏性鼻结膜炎患儿的症状和药物使用。该制剂对过敏原特异性抗体显示出显着效果,具有良好的耐受性,并且似乎是对花粉过敏的儿童的有效治疗选择。该试验已在www.clinicaltrials.gov上注册为NCT00841256。 (《过敏临床免疫杂志》 2012; 130:886-93。)

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