Sievers S, Cretich M, Gagni P, Ahrens B, Grishina G, Sampson H A, Niggemann B, Chiari M, Beyer K
Pediatric Pneumology and Immunology, Charité Universitätsmedizin, Berlin, Germany.
Department of Biology, Chemistry and Pharmacy, Free University, Berlin, Germany.
Clin Exp Allergy. 2017 Aug;47(8):1057-1068. doi: 10.1111/cea.12929. Epub 2017 May 9.
Microarray-based component-resolved diagnostics (CRD) has become an accepted tool to detect allergen-specific IgE sensitization towards hundreds of allergens in parallel from one drop of serum. Nevertheless, specificity and sensitivity as well as a simultaneous detection of allergen-specific IgG , as a potential parameter for tolerance development, remain to be optimized.
We applied the recently introduced silicon chip coated with a functional polymer named copoly(DMA-NAS-MAPS) to the simultaneous detection of food allergen-specific IgE and IgG , and compared it with ImmunoCAP and ImmunoCAP ISAC. Inter- and intraslide variation, linearity of signal and working range, sensitivity and application of internal calibrations for IgE and IgG were assessed.
Native and recombinant allergenic proteins from hen's egg and cow's milk were spotted on silicon chips coated with copoly(DMA-NAS-MAPS) along with known concentrations for human IgE and IgG . A serum pool and 105 patient samples were assessed quantitatively and semi-quantitatively with the ImmunoCAP and ImmunoCAP ISAC and correlated with IgE- and IgG -specific fluorescence on silicon microarrays.
Allergen-specific IgE and IgG were detected in parallel using two fluorescent dyes with no crosstalk. Results from the ImmunoCAP correlated better with microarray fluorescence than with ImmunoCAP ISAC except for the allergen ovomucoid. The working range of the silicon microarray for total hen's egg-specific IgE was comparable to the range of 0.1 to >100 kU /L of the ImmunoCAP system, whereas for total cow's milk, the silicon microarray was less sensitive. Detectable allergen-specific IgG could be determined only for low concentrations, but still correlated positively with ImmunoCAP results.
We confirmed the ability of the polymer coated silicon microarray to be comparably sensitive to the ImmunoCAP ISAC for various food allergens. This suggests that the copoly(DMA-NAS-MAPS) microarray is a low-cost, self-producible alternative to the commercial ImmunoCAP ISAC in allergy research.
基于微阵列的组分分辨诊断(CRD)已成为一种被认可的工具,可从一滴血清中同时检测针对数百种过敏原的过敏原特异性IgE致敏情况。然而,其特异性、敏感性以及作为耐受性发展潜在参数的过敏原特异性IgG的同时检测仍有待优化。
我们将最近推出的涂覆有功能聚合物共聚(DMA-NAS-MAPS)的硅芯片应用于食品过敏原特异性IgE和IgG的同时检测,并将其与免疫CAP和免疫CAP ISAC进行比较。评估了芯片间和芯片内的变异、信号线性和工作范围、IgE和IgG的敏感性以及内部校准的应用。
将来自鸡蛋和牛奶的天然和重组过敏原蛋白与已知浓度的人IgE和IgG一起点样在涂覆有共聚(DMA-NAS-MAPS)的硅芯片上。使用免疫CAP和免疫CAP ISAC对血清库和105份患者样本进行定量和半定量评估,并与硅微阵列上的IgE和IgG特异性荧光进行关联。
使用两种荧光染料平行检测到过敏原特异性IgE和IgG,无串扰。除了过敏原卵类粘蛋白外,免疫CAP的结果与微阵列荧光的相关性优于与免疫CAP ISAC的相关性。硅微阵列对总鸡蛋特异性IgE的工作范围与免疫CAP系统0.1至>100 kU/L的范围相当,而对于总牛奶,硅微阵列的敏感性较低。仅可在低浓度下测定可检测到的过敏原特异性IgG,但仍与免疫CAP结果呈正相关。
我们证实了涂覆聚合物的硅微阵列对各种食物过敏原的敏感性与免疫CAP ISAC相当。这表明共聚(DMA-NAS-MAPS)微阵列在过敏研究中是商业免疫CAP ISAC的低成本、可自行生产的替代方案。