Brunnée T, Seeberger A, Kleine-Tebbe J, Kunkel G
Department of Clinical Immunology and Asthma OPD, Humboldt University, Berlin, Germany.
Clin Exp Allergy. 1996 Dec;26(12):1420-7.
The ELItest is a newly developed system to measure specific IgE based on allergen bound to paper rings and an alkaline phosphatase conjugated second antibody detection system. It was compared to the CAP system, a method based on allergen conjugated to an encapsulated cellulose polymer and a beta-galactosidase conjugated fluorescence detection system.
Sera of 300 patients with positive history and positive skin-prick tests to common allergens (birch, timothy-grass, cat dander, dermatophagoides ptronyssinus, wasp venom) and 30 negative controls were tested in both systems. Serial dilutions of high titre sera were measured; inter- and intraassay coefficients of variation (cv) were determined.
The CAP system proved to be more sensitive (92.3%) compared to ELItest (84%) but marginally less specific (94.7% for CAP versus 96.7% for ELItest). Intraassay cv were slightly lower in the ELItest (7.2% CAP versus 6.4% ELItest), whereas the interassay cv was roughly twice as high for ELItest (20.1%) than for the CAP system (11.4%). Linearity over an 8-fold dilution was good in both tests (r2 0.979 ELItest versus 0.996 CAP), although ELItest levelled off at higher allergen concentrations. Similarly, correlation analysis between both systems revealed that ELItest consistently measured lower values, especially at higher concentrations of specific IgE. The slope of the linear regression line of a log/log plot of measured IgE concentrations was significantly lower than 1 in birch, cat and wasp; the y-intersect was significantly lower than 0 in all analysed allergens.
These results suggest that the ELItest system for the measurement of specific IgE is not quite as reproducible and sensitive as the CAP system but slightly more specific, and that higher concentrations of specific IgE are measured lower in the ELItest. One potential reason might be that the amount of allergen bound to a paper ring might be smaller than that bound to a cellulose polymer, but further experiments are necessary to prove this hypothesis.
ELItest是一种新开发的系统,用于基于结合在纸环上的变应原和碱性磷酸酶偶联的第二抗体检测系统来测量特异性IgE。将其与CAP系统进行比较,CAP系统是一种基于偶联到包被纤维素聚合物上的变应原和β-半乳糖苷酶偶联的荧光检测系统。
在这两种系统中对300例有常见变应原(桦树、梯牧草、猫皮屑、屋尘螨、黄蜂毒液)阳性病史和皮肤点刺试验阳性的患者血清以及30例阴性对照进行检测。对高滴度血清进行系列稀释并测量;确定批内和批间变异系数(cv)。
与ELItest(84%)相比,CAP系统被证明更敏感(92.3%),但特异性略低(CAP为94.7%,ELItest为96.7%)。ELItest的批内cv略低(CAP为7.2%,ELItest为6.4%),而ELItest的批间cv大约是CAP系统(11.4%)的两倍(20.1%)。在两种检测中,8倍稀释范围内的线性都很好(ELItest的r2为0.979,CAP为0.996),尽管ELItest在较高变应原浓度时趋于平稳。同样,两种系统之间的相关性分析表明,ELItest始终测量到较低的值,尤其是在特异性IgE浓度较高时。在桦树、猫和黄蜂中,测量的IgE浓度的对数/对数图的线性回归线斜率显著低于1;在所有分析的变应原中,y轴截距显著低于0。
这些结果表明,用于测量特异性IgE的ELItest系统不如CAP系统可重复和敏感,但特异性略高,并且在ELItest中较高浓度的特异性IgE测量值较低。一个潜在原因可能是结合在纸环上的变应原量可能小于结合在纤维素聚合物上的变应原量,但需要进一步实验来证实这一假设。