Bufe A, Ziegler-Kirbach E, Stoeckmann E, Heidemann P, Gehlhar K, Holland-Letz T, Braun W
Experimental Pneumology, Ruhr-University Bochum, Bürkle-de-la-Camp-Platz 1, Bochum, Germany.
Allergy. 2004 May;59(5):498-504. doi: 10.1111/j.1398-9995.2004.00457.x.
Local application of allergen extracts in specific immunotherapy is accompanied by increased compliance and significantly reduced side effects. However, efficacy of local immunotherapy in children has yet not been sufficiently demonstrated. This study was performed to determine clinical efficacy of high dose sublingual swallow immunotherapy (SLIT) by a double-blind placebo-controlled study in children with grass pollen allergy using high dose allergen extracts.
A total of 161 children with seasonal rhinoconjunctivitis of which, 68 had also asthma symptoms were enrolled in a multicenter double-blind placebo-controlled study for 1 year and treated on a daily basis with sublingually applied allergen drops. After 1 year all children were given treatment for another 2 years in an open-controlled setting. Symptom scores and medication were assessed during the pollen seasons with structured interviews. Applied allergen dosage, compliance, and side effects were documented by daily diary cards. Primary endpoint was a clinical index (CI) combining symptom scores with medication index. Titrated skin prick tests (SPT) and specific antibody measurements were performed each year.
Combining symptom with medication scores to CI was highly reliable (reliability coefficient = 0.89, standard error = 9.6%). Allergen-specific IgE- and IgG-subclass antibodies increased significantly in patients treated with SLIT indicating an activation of the immune response induced by the locally applied grass pollen extract. SPT reactivity did not change during therapy. After 1 year of SLIT in the original design we observed no significant difference in the CI between treatment and placebo analyzing all patients included in the study per intention to treat and per protocol. However, subgroup analysis in a repeated measures model revealed that patients with SLIT and severe symptoms before the beginning of treatment (CI > mean/ > 1.51) showed a significant improvement of clinical symptoms after 3 years.
In this study SLIT was accompanied by a significant placebo effect. Efficacy of treatment could only be seen in children with severe clinical symptoms and this became clinically marked after 3 years of therapy.
在特异性免疫治疗中局部应用变应原提取物可提高依从性并显著减少副作用。然而,局部免疫治疗在儿童中的疗效尚未得到充分证实。本研究旨在通过一项双盲安慰剂对照研究,使用高剂量变应原提取物来确定高剂量舌下含服免疫治疗(SLIT)对草花粉过敏儿童的临床疗效。
共有161例季节性鼻结膜炎儿童(其中68例也有哮喘症状)参加了一项多中心双盲安慰剂对照研究,为期1年,每天接受舌下含服变应原滴剂治疗。1年后,所有儿童在开放对照环境中再接受2年治疗。在花粉季节通过结构化访谈评估症状评分和用药情况。应用的变应原剂量、依从性和副作用通过每日日记卡记录。主要终点是将症状评分与用药指数相结合的临床指数(CI)。每年进行滴定皮肤点刺试验(SPT)和特异性抗体检测。
将症状评分与用药评分结合为CI具有高度可靠性(可靠性系数=0.89,标准误差=9.6%)。接受SLIT治疗的患者中,变应原特异性IgE和IgG亚类抗体显著增加,表明局部应用草花粉提取物诱导的免疫反应被激活。治疗期间SPT反应性未改变。在最初设计的SLIT治疗1年后,按照意向性分析和符合方案分析纳入研究的所有患者,治疗组与安慰剂组的CI无显著差异。然而,重复测量模型的亚组分析显示,治疗开始前有严重症状(CI>平均值/>1.51)的SLIT患者在3年后临床症状有显著改善。
在本研究中,SLIT伴有显著的安慰剂效应。治疗效果仅在有严重临床症状的儿童中可见,且在治疗3年后临床效果明显。