Park J W, Kim K S, Jin H S, Kim C W, Kang D B, Choi S Y, Yong T-S, Oh S H, Hong C-S
Department of Internal Medicine, Institute of Allergy, Yonsei University College of Medicine, Seoul, Korea.
Clin Exp Allergy. 2002 Jul;32(7):1042-7. doi: 10.1046/j.1365-2222.2002.01421.x.
Der p 2 isoallergens have been reported and the possibility of different allergenicity has also been suggested. In addition, the quantification with 2-site ELISA may be affected by the isoallergens.
Two different recombinant Der p 2 (rDer p 2) isoallergens were compared in terms of human IgE responses and the reliability of quantification of them with two-site ELISA kits which use monoclonal antibodies (mAbs) as capture and detection of Der p 2.
Seven different Der p 2 cDNA from the cultured Dermatophagoides pteronyssinus (DP) were cloned and polymorphism in nine amino acid residues was found. Two different recombinant isoallergens (rDer p 2A and rDer p 2B) were expressed and compared to their human IgE immune responses by ELISA and the ELISA inhibition test with 23 sera of DP-allergic patients. The reliability of quantification of two different available 2-site ELISA kits, which used mAbs for capture and detection of Der p 2, was evaluated.
The ELISA optical density of rDer p 2B-specific IgE (sIgE) was higher than that of rDer p 2A (P < 0.001). The ELISA inhibition curve of rDer p 2B sIgE in pool I sera (n = 5; high sIgE both to rDer p 2A and rDer p 2B) did not show any differences in the 50% inhibition concentration and maximum inhibitory percentage of rDer p 2A and rDer p 2B sIgE. However, with pool II sera (n = 5; markedly higher sIgE to rDer p 2B than rDer p 2A), the 50% inhibitory concentrations (10 microg/mL vs. 40 ng/mL) and maximum inhibitory percentage (61% vs. 99%) of rDer p 2B sIgE with the two recombinant isoallergens were quite different. rDer p 2B could be quantified with two different 2-site ELISA kits, but rDer p 2A was detected by only one kit.
We conclude that isoallergens of Der p 2 may have different IgE immune responses. Quantification of Der p 2 with 2-site ELISA kits that adopted mAbs, might be affected by the prevalent form of the isoallergens in reservoir dust.
已报道了Der p 2同种变应原,并且也有人提出了不同变应原性的可能性。此外,双位点ELISA定量可能会受到同种变应原的影响。
比较两种不同的重组Der p 2(rDer p 2)同种变应原在人IgE反应方面的差异,以及使用单克隆抗体(mAb)作为捕获和检测Der p 2的双位点ELISA试剂盒对其进行定量的可靠性。
从培养的粉尘螨(DP)中克隆出7种不同的Der p 2 cDNA,发现9个氨基酸残基存在多态性。表达了两种不同的重组同种变应原(rDer p 2A和rDer p 2B),并通过ELISA和对23例DP过敏患者血清进行的ELISA抑制试验比较它们的人IgE免疫反应。评估了两种不同的可用双位点ELISA试剂盒(使用mAb捕获和检测Der p 2)定量的可靠性。
rDer p 2B特异性IgE(sIgE)的ELISA光密度高于rDer p 2A(P < 0.001)。I组血清(n = 5;对rDer p 2A和rDer p 2B的sIgE均高)中rDer p 2B sIgE的ELISA抑制曲线在rDer p 2A和rDer p 2B sIgE的50%抑制浓度和最大抑制百分比方面未显示任何差异。然而,对于II组血清(n = 5;对rDer p 2B的sIgE明显高于rDer p 2A),两种重组同种变应原的rDer p 2B sIgE的50%抑制浓度(10μg/mL对40 ng/mL)和最大抑制百分比(61%对99%)有很大差异。rDer p 2B可用两种不同的双位点ELISA试剂盒进行定量,但rDer p 2A仅能被一种试剂盒检测到。
我们得出结论,Der p 2的同种变应原可能具有不同的IgE免疫反应。采用mAb的双位点ELISA试剂盒对Der p 2进行定量可能会受到储尘中同种变应原流行形式的影响。