Duc J, Peitrequin R, Pécoud A
Department of Medicine, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
Allergy. 1988 Jul;43(5):332-7. doi: 10.1111/j.1398-9995.1988.tb00426.x.
Phadiatop (Pharmacia) is a new in vitro screening test for respiratory allergy which detects in serum the presence of specific IgE to a mixture of common inhalant allergens; results are either positive or negative. Among 100 patients suffering from rhinitis and/or asthma, investigated with 15 skin prick tests (SPT) and RAST for frequent allergens, the Phadiatop was positive in 63: all 63 had at least one positive SPT and RAST (specificity: 100%). Conversely, ther were 67 patients who had a positive RAST for at least one allergen: among these 67 the total IgE concentration in serum was high (greater than 100 kU/l) in 43 (64%) and the Phadiatop was positive in 63 (94%). Phadiatop was negative in serum obtained from 10 cord bloods and 10 non-allergic subjects (disease-free, 15 negative SPT and RAST). Results of the radio-immunoassay originally proposed by the manufacturer were similar to those obtained with a modified enzymo assay using a fluorometric substrate. In the prediction of respiratory allergy, Phadiatop was found to be specific and more accurate than the determination of total IgE in serum.
Phadiatop(法玛西亚公司)是一种用于呼吸道过敏的新型体外筛查试验,可检测血清中针对常见吸入性变应原混合物的特异性IgE;结果为阳性或阴性。在100例患有鼻炎和/或哮喘的患者中,用15种常见变应原的皮肤点刺试验(SPT)和放射性变应原吸附试验(RAST)进行检测,Phadiatop试验结果阳性者63例:这63例患者的SPT和RAST至少有一项为阳性(特异性:100%)。相反,有67例患者至少对一种变应原的RAST结果为阳性:在这67例患者中,43例(64%)血清总IgE浓度较高(大于100 kU/l),Phadiatop试验结果阳性者63例(94%)。从10份脐血和10名非过敏受试者(无疾病,15项SPT和RAST结果均为阴性)获得的血清中,Phadiatop试验结果为阴性。制造商最初提出的放射免疫分析结果与使用荧光底物的改良酶分析结果相似。在呼吸道过敏的预测中,发现Phadiatop试验具有特异性,且比血清总IgE测定更准确。