Eng P A, Reinhold M, Gnehm H P E
Department of Pediatrics, Kantonsspital Aarau, Switzerland.
Allergy. 2002 Apr;57(4):306-12. doi: 10.1034/j.1398-9995.2002.1o3264.x.
In a previous controlled study we demonstrated that preseasonal grass pollen immunotherapy for three years was effective in children. In the current study we examined the same group of patients to see if there is still a benefit six years after discontinuation of treatment.
Thirteen of 14 patients with previous specific immunotherapy (SIT) and 10 out of 14 patients of the control group were prospectively followed during the grass pollen season. Outcome measures were seasonal symptom scores for eyes, nose and chest, the use of symptomatic medication and visual analog scale. Objective measures included skin prick test reactivity to seasonal and perennial allergens and conjunctival provocation testing.
During the 13 week observation time scores for overall hayfever symptoms (P < 0.004) and individual symptoms for eyes (P < 0.02), nose (P < 0.04) and chest (P < 0.01) as well as combined symptom and medication scores (P < 0.002) remained lower in the group with previous SIT. Only 23% of patients with previous pollen-asthma who had received SIT experienced pollen-associated lower respiratory tract symptoms compared to 70% in the control group (P < 0.05). There was no significant difference in the use of pharmacological treatment during the pollen season except for asthma medication. The average visual analog scale was lower in the post-SIT group (P < 0.05). Six years after cessation of SIT the immediate skin response to grass pollen remained decreased compared to the reaction of the controls (P < 0.01). There was also a tendency for higher allergen concentration to provoke a conjunctival response in the post-SIT group but without reaching statistical significance. Eight years after commencement of SIT, 61% of the initially pollen-monosensitized children had developed new sensitization to perennial allergens compared to 100% in the control group (P < 0.05).
There is still a significant clinical benefit six years after discontinuation of preseasonal grass pollen immunotherapy in childhood. SIT in children with pollen-allergy reduces onset of new sensitization and therefore has the potential to modify the natural course of allergic disease.
在之前的一项对照研究中,我们证明了对儿童进行为期三年的季节性草花粉免疫疗法是有效的。在当前的研究中,我们对同一组患者进行了检查,以观察在停止治疗六年之后是否仍有获益。
在草花粉季节对14名曾接受特异性免疫疗法(SIT)的患者中的13名以及对照组14名患者中的10名进行前瞻性随访。观察指标为眼睛、鼻子和胸部的季节性症状评分、对症药物的使用情况以及视觉模拟量表。客观指标包括对季节性和常年性过敏原的皮肤点刺试验反应性以及结膜激发试验。
在为期13周的观察期内,曾接受SIT治疗的组中,总体花粉症症状评分(P < 0.004)以及眼睛(P < 0.02)、鼻子(P < 0.04)和胸部(P < 0.01)的个体症状评分以及综合症状和药物评分(P < 0.002)均较低。曾接受SIT治疗的既往花粉性哮喘患者中只有23%出现了与花粉相关的下呼吸道症状,而对照组中这一比例为70%(P < 0.05)。除哮喘药物外,花粉季节期间药物治疗的使用情况没有显著差异。SIT治疗后组的平均视觉模拟量表得分较低(P < 0.05)。停止SIT治疗六年之后,与对照组相比,对草花粉的即刻皮肤反应仍然降低(P < 0.01)。在SIT治疗后组中,也存在较高的过敏原浓度引发结膜反应的趋势,但未达到统计学显著性。在开始SIT治疗八年之后,最初对花粉单一致敏的儿童中有61%对常年性过敏原产生了新的致敏,而对照组中这一比例为100%(P < 0.05)。
儿童季节性草花粉免疫疗法停止治疗六年之后仍有显著的临床获益。对花粉过敏的儿童进行SIT可减少新致敏的发生,因此有可能改变过敏性疾病的自然病程。