Seyfarth Florian, Schliemann Sibylle, Wiegand Cornelia, Hipler Uta-Christina, Elsner Peter
Department of Dermatology, Jena University Hospital, Erfurter Straße 35, 07740, Jena, Germany.
Int Arch Occup Environ Health. 2014;87(7):775-81. doi: 10.1007/s00420-013-0921-6. Epub 2013 Dec 6.
Latex allergy can be diagnosed by different test methods such as IgE quantification, Western blot, cellular antigen stimulation test (CAST), and in vivo methods [e.g. skin prick test (SPT)]. Phadia provides two modern methods using recombinant latex allergens: ImmunoCAP(®) and the Immuno Solid-phase Allergen Chip (ISAC(®)), which enables simultaneous determination of specific IgE against five latex allergens. We compared the diagnostic sensitivity of the ISAC(®) test kit and the conventional Hev b 5-spiked ImmunoCAP(®) latex extract.
Forty sera were sampled from subjects with suspected natural rubber latex (NRL) allergy. These patients had positive SPT to NRL extract, positive NRL Western blots, and positive results in the CAST. All sera were analysed using the ISAC(®) and recombinant NRL ImmunoCAP(®) allergens and compared to the results of 20 negative control sera.
Only 22 of the 40 subjects (55 %) showed positivity to at least one latex allergen on the ISAC(®) (sensitivity ISAC(®) 55 %). The sensitivity of the ImmunoCAP(®) latex extract was 70 %. The most frequently detected sensitization was against Hev b 6.01 (n = 12). When the serum samples were tested with all recombinant ImmunoCAP(®) allergens, three additional sensitizations against latex could be detected compared to the ISAC(®).
Microarrays do offer many potential benefits such as elegant simultaneous determination of sensitizations against different NRL allergens with minimal amounts of serum. However, a negative NRL test result should be regarded with caution and at least be confirmed by other in vitro methods.
乳胶过敏可通过不同的检测方法进行诊断,如免疫球蛋白E(IgE)定量检测、蛋白质印迹法、细胞抗原刺激试验(CAST)以及体内检测方法[如皮肤点刺试验(SPT)]。法迪亚公司提供了两种使用重组乳胶过敏原的现代检测方法:ImmunoCAP(®)和免疫固相过敏原芯片(ISAC(®)),后者能够同时测定针对五种乳胶过敏原的特异性IgE。我们比较了ISAC(®)检测试剂盒与传统的添加了Hev b 5的ImmunoCAP(®)乳胶提取物的诊断敏感性。
从疑似天然橡胶乳胶(NRL)过敏的受试者中采集了40份血清样本。这些患者对NRL提取物的皮肤点刺试验呈阳性、NRL蛋白质印迹法呈阳性且CAST结果为阳性。所有血清样本均使用ISAC(®)和重组NRL ImmunoCAP(®)过敏原进行分析,并与20份阴性对照血清的结果进行比较。
40名受试者中只有22名(55%)在ISAC(®)检测中对至少一种乳胶过敏原呈阳性反应(ISAC(®)敏感性为55%)。ImmunoCAP(®)乳胶提取物的敏感性为70%。最常检测到的致敏原是Hev b 6.01(n = 12)。当血清样本用所有重组ImmunoCAP(®)过敏原进行检测时,与ISAC(®)相比,可检测到另外三种针对乳胶的致敏反应。
微阵列确实具有许多潜在优势,例如能够以最少的血清量优雅地同时测定针对不同NRL过敏原的致敏反应。然而,NRL检测结果为阴性时应谨慎对待,至少需通过其他体外方法进行确认。