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Biological equilibration of allergen preparations: methodological aspects and reproducibility
Authors:S. DREBORG,A. BASOMBA¶    ,L. BELIN&Dagger  ,S. DURHAM,R. EINARSSON&dagger  ,N. E. ERIKSSON§  ,A. B. FROSTAD,Ø  ,GRIMMER,R. HALVORSEN,M. HOLGERSSON,A. B. KAY,G. NILSSON,H.-J. MALLING§  §  ,I. SJÖ  GREN&dagger  ,B. WEEKE§  §  ,I.-J. VÅ  LA&Dagger  &Dagger  ,O. ZETTERSTRÖ    
Affiliation:Department of Paediatrics, University Hospital, Linköping;Pharmacia Diagnostics AB, Sweden;Akademiska Hospital, Uppsala, Sweden;Sahlgrenska Hospital, Göteborg, Sweden;Länssjukhuset, Halmatad, Sweden;Karolinska Hospital, Stockholm, Sweden;Nycomed, Oslo, Norway;Kristiansand, Norway;Rigshospitalet, Copenhagen, Denmark;Hospital "La Fe" Valencia, Spain;Cardiothoracic Institute, Brompton Hospital, London, U.K.
Abstract: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 < 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 < 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.
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