Ostergaard P A, Kaad P H, Kristensen T
Allergy. 1986 Nov;41(8):588-93. doi: 10.1111/j.1398-9995.1986.tb00351.x.
One hundred and six of 503 (21%) consecutive children with asthma, who from 1979 to 1983 commenced hyposensitization therapy, were prospectively studied on the safety of immunotherapy. More than 80% of the patients completed therapy without side effects. Thirteen patients were withdrawn from hyposensitization due to moderate and predictable, but intolerable, side effects such as asthma/rhinitis, urticaria and subcutaneous nodules and hypersensitivity to aluminium. However, more alarming was the outcome in six children, who after an uneventful course of immunotherapy and after several months on maintenance therapy, suddenly, 5 to 20 min (mean 10 min) following an earlier tolerable allergen injection, developed severe, anaphylactic reactions, in three of them nearly fatal. Mould extracts were responsible for the most frequent and serious side effects (Alternaria iridis/alternata, 3 patients, Cladosporium herbarum, 8 patients). Furthermore, serious, but not immediately life-threatening, anaphylactic reactions occurred in two children treated with Phleum pratense. On the other hand, hyposensitization with Dermatophagoides pteronyssinus was very well tolerated.
对1979年至1983年开始进行减敏治疗的503例连续性哮喘患儿中的106例(21%)进行了免疫治疗安全性的前瞻性研究。超过80%的患者完成治疗且无副作用。13例患者因出现中度且可预测但无法耐受的副作用(如哮喘/鼻炎、荨麻疹、皮下结节以及对铝过敏)而退出减敏治疗。然而,更令人担忧的是6名儿童的情况,他们在免疫治疗过程顺利且维持治疗数月后,在之前可耐受的过敏原注射后5至20分钟(平均10分钟)突然出现严重的过敏反应,其中3例近乎致命。霉菌提取物导致了最常见且最严重的副作用(鸢尾/交替链格孢,3例;草本枝孢菌,8例)。此外,2例接受梯牧草治疗的儿童出现了严重但未立即危及生命的过敏反应。另一方面,对粉尘螨进行减敏治疗的耐受性非常好。