Division of Allergy, Department of Internal Medicine, Tepecik Training and Research Hospital, İzmir, Turkey.
Int Arch Allergy Immunol. 2012;158(3):281-7. doi: 10.1159/000332929. Epub 2012 Mar 6.
The precision of the methods used to diagnose latex allergy is of great importance due to false-positive results. Neither the skin prick test (SPT) nor the latex-specific IgE assay has 100% diagnostic accuracy. We analysed the diagnostic value of latex-specific IgE by the first-ever concomitant use of the SPT and nasal provocation test (NPT).
Twenty-seven latex-sensitive patients (group 1), 46 aeroallergen-sensitive patients (group 2a) and 33 healthy subjects (group 2b) participated in the study. All groups underwent an SPT with latex and aeroallergens and an NPT with latex. Latex-specific IgE and total IgE levels were measured by the ImmunoCAP assay.
Latex-specific IgE was positive in 92.6, 30.4 and 9.1% of groups 1, 2a and 2b, respectively. The 11 aeroallergen-sensitive patients in group 1 and all of the patients in group 2a were predominantly sensitised to pollens (grass, weed and tree) and reacted to a lesser degree to house dust mite, moulds and animal dander. Combined pollinosis was remarkably more prevalent in patients with positive latex-specific IgE in group 2a than in those with negative latex-specific IgE (p = 0.001). The NPT was positive in 84.6% of group 1 and negative in all control subjects. The sensitivity, specificity, negative predictive value and positive predictive value of the latex-specific IgE assay were 90.9, 72.2, 96.3 and 50%, respectively.
The high rate of false-positive results for latex-specific IgE by ImmunoCAP should be taken into account when making a diagnosis of latex allergy in patients with pollinosis, especially in those sensitised to more than one pollen species.
由于假阳性结果,用于诊断乳胶过敏的方法的精确性非常重要。皮肤点刺试验(SPT)和乳胶特异性 IgE 检测均没有 100%的诊断准确性。我们通过首次同时使用 SPT 和鼻激发试验(NPT)来分析乳胶特异性 IgE 的诊断价值。
27 例乳胶过敏患者(组 1)、46 例气传过敏原过敏患者(组 2a)和 33 例健康对照者(组 2b)参与了研究。所有组均接受了乳胶和气传过敏原的 SPT 和 NPT,乳胶特异性 IgE 和总 IgE 水平通过 ImmunoCAP 检测进行测量。
组 1、组 2a 和组 2b 中乳胶特异性 IgE 阳性的比例分别为 92.6%、30.4%和 9.1%。组 1 中的 11 例气传过敏原过敏患者和组 2a 中的所有患者主要对花粉(草、杂草和树木)过敏,对屋尘螨、霉菌和动物皮屑的反应程度较低。组 2a 中乳胶特异性 IgE 阳性患者的合并花粉过敏明显多于乳胶特异性 IgE 阴性患者(p = 0.001)。组 1 中有 84.6%的患者 NPT 阳性,而所有对照组均为阴性。乳胶特异性 IgE 检测的敏感性、特异性、阴性预测值和阳性预测值分别为 90.9%、72.2%、96.3%和 50%。
在花粉过敏患者中,尤其是在对多种花粉过敏的患者中,使用 ImmunoCAP 检测乳胶特异性 IgE 会产生较高的假阳性率,应考虑到这一点。