Dreborg S, Basomba A, Belin L, Durham S, Einarsson R, Eriksson N E, Frostad A B, Grimmer O, Halvorsen R, Holgersson M
Department of Paediatrics, University Hospital, Linköping, Sweden.
Clin Allergy. 1987 Nov;17(6):537-50. doi: 10.1111/j.1365-2222.1987.tb02050.x.
A method for biological equilibration (BE) of allergen reference preparations using the skin-prick test (SPT) method and histamine HCl 10 mg/ml as reference substance (reference method), was evaluated. The precision was low for weals less than 10 mm2. The slope (log weal area/log concentration) of allergen and histamine did not vary significantly between investigators and allergens. The median slopes were 0.39 (n = 384) and 0.34 (n = 397), for allergen and histamine, respectively (P less than 0.01). The concentration of allergen eliciting a weal of the same size as that of histamine HCl 1 mg/ml (Chl) in the median sensitive patient, 1000 Biological Units/ml (BU/ml), did not vary significantly between clinics/geographical regions (grasses, mites and moulds). As BE is repeatable between regions, BUs estimated by this method are generally valid. A high correlation (r = 0.91, P less than 0.001) was found between the median Chl as estimated with histamine 1 and 10 mg/ml as reference substance, respectively. Thus, this reference method for BE is valid. The precision of the SPT method with histamine HCl 1 mg/ml is not as good as with 10 mg/ml, which is therefore recommended as the reference concentration.
评估了一种使用皮肤点刺试验(SPT)方法以及10 mg/ml盐酸组胺作为参考物质(参考方法)对变应原参考制剂进行生物平衡(BE)的方法。对于小于10 mm2的风团,精密度较低。变应原和组胺的斜率(log风团面积/log浓度)在研究者和变应原之间没有显著差异。变应原和组胺的中位数斜率分别为0.39(n = 384)和0.34(n = 397)(P小于0.01)。在中位敏感患者中,引起与1 mg/ml盐酸组胺相同大小风团的变应原浓度(Chl),即1000生物单位/毫升(BU/ml),在各诊所/地理区域(草、螨和霉菌)之间没有显著差异。由于BE在各区域之间具有可重复性,通过该方法估算的BU通常是有效的。分别以1 mg/ml和10 mg/ml组胺作为参考物质估算的中位Chl之间存在高度相关性(r = 0.91,P小于0.001)。因此,这种BE参考方法是有效的。1 mg/ml盐酸组胺的SPT方法的精密度不如10 mg/ml的,因此推荐10 mg/ml作为参考浓度。